Reação de Negishi (Portuguese Wikipedia)

Analysis of information sources in references of the Wikipedia article "Reação de Negishi" in Portuguese language version.

refsWebsite

Global rank Portuguese rank

44doi.org

2^nd place

4^th place

28nih.gov

4^th place

8^th place

15worldcat.org

5^th place

4acs.org

1,248^th place

1,143^rd place

4wiley.com

222^nd place

196^th place

3orgsyn.org

2,971^st place

3,512^th place

1harvard.edu

18^th place

51^st place

1rsc.org

2,020^th place

2,232^nd place

1zenodo.org

621^st place

1,847^th place

acs.org

pubs.acs.org

Zhou, Jianrong (Steve); Fu, Gregory C. (dezembro de 2003). «Cross-Couplings of Unactivated Secondary Alkyl Halides: Room-Temperature Nickel-Catalyzed Negishi Reactions of Alkyl Bromides and Iodides». Journal of the American Chemical Society (em inglês). 125 (48): 14726–14727. ISSN 0002-7863. PMID 14640646. doi:10.1021/ja0389366
Fischer, Christian; Fu, Gregory C. (abril de 2005). «Asymmetric Nickel-Catalyzed Negishi Cross-Couplings of Secondary α-Bromo Amides with Organozinc Reagents». Journal of the American Chemical Society (em inglês). 127 (13): 4594–4595. ISSN 0002-7863. PMID 15796523. doi:10.1021/ja0506509
Son, Sunghee; Fu, Gregory C. (1 de março de 2008). «Nickel-Catalyzed Asymmetric Negishi Cross-Couplings of Secondary Allylic Chlorides with Alkylzincs». Journal of the American Chemical Society (em inglês). 130 (9): 2756–2757. ISSN 0002-7863. PMID 18257579. doi:10.1021/ja800103z
Sase, Shohei; Jaric, Milica; Metzger, Albrecht; Malakhov, Vladimir; Knochel, Paul (19 de setembro de 2008). «One-Pot Negishi Cross-Coupling Reactions of In Situ Generated Zinc Reagents with Aryl Chlorides, Bromides, and Triflates». The Journal of Organic Chemistry (em inglês). 73 (18): 7380–7382. ISSN 0022-3263. PMID 18693766. doi:10.1021/jo801063c

doi.org

dx.doi.org

King, Anthony O.; Okukado, Nobuhisa; Negishi, Ei-ichi (1977). «Highly general stereo-, regio-, and chemo-selective synthesis of terminal and internal conjugated enynes by the Pd-catalysed reaction of alkynylzinc reagents with alkenyl halides». Journal of the Chemical Society, Chemical Communications (19). 683 páginas. doi:10.1039/C39770000683
Zhou, Jianrong (Steve); Fu, Gregory C. (dezembro de 2003). «Cross-Couplings of Unactivated Secondary Alkyl Halides: Room-Temperature Nickel-Catalyzed Negishi Reactions of Alkyl Bromides and Iodides». Journal of the American Chemical Society (em inglês). 125 (48): 14726–14727. ISSN 0002-7863. PMID 14640646. doi:10.1021/ja0389366
Negishi, Eiichi; King, Anthony O.; Okukado, Nobuhisa (1 de maio de 1977). «Selective carbon-carbon bond formation via transition metal catalysis. 3. A highly selective synthesis of unsymmetrical biaryls and diarylmethanes by the nickel- or palladium-catalyzed reaction of aryl- and benzylzinc derivatives with aryl halides». The Journal of Organic Chemistry. 42 (10): 1821–1823. ISSN 0022-3263. doi:10.1021/jo00430a041
Gavryushin, Andrei; Kofink, Christiane; Manolikakes, Georg; Knochel, Paul (1 de outubro de 2005). «Efficient Cross-Coupling of Functionalized Arylzinc Halides Catalyzed by a Nickel Chloride−Diethyl Phosphite System». Organic Letters. 7 (22): 4871–4874. ISSN 1523-7060. PMID 16235910. doi:10.1021/ol051615+
Baba S, Negishi E (1976). «A novel stereospecific alkenyl-alkenyl cross-coupling by a palladium- or nickel-catalyzed reaction of alkenylalanes with alkenyl halides». Journal of the American Chemical Society. 98 (21): 6729–6731. doi:10.1021/ja00437a067
Negishi E, King AO, Okukado N (1977). «Selective carbon-carbon bond formation via transition metal catalysis. 3. A highly selective synthesis of unsymmetrical biaryls and diarylmethanes by the nickel- or palladium-catalyzed reaction of aryl- and benzylzinc derivatives with aryl halides». The Journal of Organic Chemistry. 42 (10): 1821–1823. doi:10.1021/jo00430a041
Casado AL, Espinet P (1998). «On the Configuration Resulting from Oxidative Addition of RX to Pd(PPh3)4 and the Mechanism of the cis-to-trans Isomerization of [PdRX(PPh3)2] Complexes (R = Aryl, X = Halide)». Organometallics. 17 (5): 954–959. doi:10.1021/om9709502
McCann LC, Hunter HN, Clyburne JA, Organ MG (julho de 2012). «Higher-order zincates as transmetalators in alkyl-alkyl negishi cross-coupling». Angewandte Chemie. 51 (28): 7024–7. PMID 22685029. doi:10.1002/anie.201203547
García-Melchor M, Braga AA, Lledós A, Ujaque G, Maseras F (novembro de 2013). «Computational perspective on Pd-catalyzed C-C cross-coupling reaction mechanisms». Accounts of Chemical Research. 46 (11): 2626–34. PMID 23848308. doi:10.1021/ar400080r
Casares JA, Espinet P, Fuentes B, Salas G (março de 2007). «Insights into the mechanism of the Negishi reaction: ZnRX versus ZnR2 reagents». Journal of the American Chemical Society. 129 (12): 3508–9. PMID 17328551. doi:10.1021/ja070235b
Fuentes B, García-Melchor M, Lledós A, Maseras F, Casares JA, Ujaque G, Espinet P (agosto de 2010). «Palladium round trip in the Negishi coupling of trans-[PdMeCl(PMePh2)2] with ZnMeCl: an experimental and DFT study of the transmetalation step». Chemistry. 16 (29): 8596–9. PMID 20623568. doi:10.1002/chem.201001332
Liu Q, Lan Y, Liu J, Li G, Wu YD, Lei A (julho de 2009). «Revealing a second transmetalation step in the Negishi coupling and its competition with reductive elimination: improvement in the interpretation of the mechanism of biaryl syntheses». Journal of the American Chemical Society. 131 (29): 10201–10. PMID 19572717. doi:10.1021/ja903277d
Phapale, Vilas B.; Cárdenas, Diego J. (27 de maio de 2009). «Nickel-catalysed Negishi cross-coupling reactions: scope and mechanisms». Chemical Society Reviews (em inglês). 38 (6): 1598–1607. ISSN 1460-4744. PMID 19587955. doi:10.1039/B805648J
Schley, Nathan D.; Fu, Gregory C. (26 de novembro de 2014). «Nickel-Catalyzed Negishi Arylations of Propargylic Bromides: A Mechanistic Investigation». Journal of the American Chemical Society. 136 (47): 16588–16593. ISSN 0002-7863. PMC 4277758. PMID 25402209. doi:10.1021/ja508718m
Morrell, Dennis G.; Kochi, Jay K. (1 de dezembro de 1975). «Mechanistic studies of nickel catalysis in the cross coupling of aryl halides with alkylmetals. Role of arylalkylnickel(II) species as intermediates». Journal of the American Chemical Society. 97 (25): 7262–7270. ISSN 0002-7863. doi:10.1021/ja00858a011
Yu Y, Bond AD, Leonard PW, Lorenz UJ, Timofeeva TV, Vollhardt KP, Whitener GD, Yakovenko AA (junho de 2006). «Hexaferrocenylbenzene». Chemical Communications (24): 2572–4. PMID 16779481. doi:10.1039/b604844g
Zhao Y, Wang H, Hou X, Hu Y, Lei A, Zhang H, Zhu L (novembro de 2006). «Oxidative cross-coupling through double transmetallation: surprisingly high selectivity for palladium-catalyzed cross-coupling of alkylzinc and alkynylstannanes». Journal of the American Chemical Society. 128 (47): 15048–9. PMID 17117830. doi:10.1021/ja0647351
Yang Y, Oldenhuis NJ, Buchwald SL (janeiro de 2013). «Mild and general conditions for negishi cross-coupling enabled by the use of palladacycle precatalysts». Angewandte Chemie. 52 (2): 615–9. PMC 3697109. PMID 23172689. doi:10.1002/anie.201207750
Giovannini, Riccardo; Stüdemann, Thomas; Dussin, Gaelle; Knochel, Paul (1998). «An Efficient Nickel-Catalyzed Cross-Coupling Between sp3 Carbon Centers». Angewandte Chemie International Edition (em inglês). 37 (17): 2387–2390. ISSN 1521-3773. PMID 29710957. doi:10.1002/(SICI)1521-3773(19980918)37:17<2387::AID-ANIE2387>3.0.CO;2-M
Jensen, Anne Eeg; Knochel, Paul (1 de janeiro de 2002). «Nickel-Catalyzed Cross-Coupling between Functionalized Primary or Secondary Alkylzinc Halides and Primary Alkyl Halides». The Journal of Organic Chemistry. 67 (1): 79–85. ISSN 0022-3263. PMID 11777442. doi:10.1021/jo0105787
Giovannini, Riccardo; Knochel, Paul (1 de novembro de 1998). «Ni(II)-Catalyzed Cross-Coupling between Polyfunctional Arylzinc Derivatives and Primary Alkyl Iodides». Journal of the American Chemical Society. 120 (43): 11186–11187. ISSN 0002-7863. doi:10.1021/ja982520o
Fischer, Christian; Fu, Gregory C. (abril de 2005). «Asymmetric Nickel-Catalyzed Negishi Cross-Couplings of Secondary α-Bromo Amides with Organozinc Reagents». Journal of the American Chemical Society (em inglês). 127 (13): 4594–4595. ISSN 0002-7863. PMID 15796523. doi:10.1021/ja0506509
Son, Sunghee; Fu, Gregory C. (1 de março de 2008). «Nickel-Catalyzed Asymmetric Negishi Cross-Couplings of Secondary Allylic Chlorides with Alkylzincs». Journal of the American Chemical Society (em inglês). 130 (9): 2756–2757. ISSN 0002-7863. PMID 18257579. doi:10.1021/ja800103z
Phapale, Vilas B.; Buñuel, Elena; García-Iglesias, Miguel; Cárdenas, Diego J. (2007). «Ni-Catalyzed Cascade Formation of C(sp3)C(sp3) Bonds by Cyclization and Cross-Coupling Reactions of Iodoalkanes with Alkyl Zinc Halides». Angewandte Chemie International Edition. 46 (46): 8790–8795. ISSN 1521-3773. PMID 17918274. doi:10.1002/anie.200702528
Johansson Seechurn CC, Kitching MO, Colacot TJ, Snieckus V (maio de 2012). «Palladium-catalyzed cross-coupling: a historical contextual perspective to the 2010 Nobel Prize». Angewandte Chemie. 51 (21): 5062–85. PMID 22573393. doi:10.1002/anie.201107017
Sase S, Jaric M, Metzger A, Malakhov V, Knochel P (setembro de 2008). «One-pot Negishi cross-coupling reactions of in situ generated zinc reagents with aryl chlorides, bromides, and triflates». The Journal of Organic Chemistry. 73 (18): 7380–2. PMID 18693766. doi:10.1021/jo801063c
Manley PW, Acemoglu M, Marterer W, Pachinger W (2003). «Large-Scale Negishi Coupling as Applied to the Synthesis of PDE472, an Inhibitor of Phosphodiesterase Type 4D». Organic Process Research & Development. 7 (3): 436–445. doi:10.1021/op025615q
Torborg C, Beller M (2009). «Recent Applications of Palladium-Catalyzed Coupling Reactions in the Pharmaceutical, Agrochemical, and Fine Chemical Industries». Advanced Synthesis & Catalysis. 351 (18): 3027–3043. doi:10.1002/adsc.200900587
Nicolaou KC, Bulger PG, Sarlah D (julho de 2005). «Palladium-catalyzed cross-coupling reactions in total synthesis». Angewandte Chemie. 44 (29): 4442–89. PMID 15991198. doi:10.1002/anie.200500368
Lessene G (2004). «Advances in the Negishi coupling». Aust. J. Chem. 57 (1). 107 páginas. doi:10.1071/ch03225
Torssell S, Wanngren E, Somfai P (maio de 2007). «Total synthesis of (-)-stemoamide». The Journal of Organic Chemistry. 72 (11): 4246–9. PMID 17451274. doi:10.1021/jo070498o
Aoyagi S, Hirashima S, Saito K, Kibayashi C (2002). «Convergent Approach to Pumiliotoxin Alkaloids. Asymmetric Total Synthesis of (+)-Pumiliotoxins A, B, and 225F». The Journal of Organic Chemistry. 67 (16): 5517–5526. PMID 12153249. doi:10.1021/jo0200466
Maloney DJ, Hecht SM (setembro de 2005). «A stereocontrolled synthesis of delta-trans-tocotrienoloic acid». Organic Letters. 7 (19): 4297–300. PMID 16146411. doi:10.1021/ol051849t
Smith, Sean W.; Fu, Gregory C. (2008). «Nickel-Catalyzed Negishi Cross-Couplings of Secondary Nucleophiles with Secondary Propargylic Electrophiles at Room Temperature». Angewandte Chemie International Edition. 47 (48): 9334–9336. ISSN 1521-3773. PMC 2790060. PMID 18972493. doi:10.1002/anie.200802784
Schmidt, Thomas; Kirschning, Andreas (2012). «Total Synthesis of Carolacton, a Highly Potent Biofilm Inhibitor». Angewandte Chemie International Edition. 51 (4): 1063–1066. ISSN 1521-3773. PMID 22162345. doi:10.1002/anie.201106762
Huo S (fevereiro de 2003). «Highly efficient, general procedure for the preparation of alkylzinc reagents from unactivated alkyl bromides and chlorides». Organic Letters. 5 (4): 423–5. PMID 12583734. doi:10.1021/ol0272693
Giovannini R, Knochel P (1998). «Ni(II)-Catalyzed Cross-Coupling between Polyfunctional Arylzinc Derivatives and Primary Alkyl Iodides». Journal of the American Chemical Society. 120 (43): 11186–11187. doi:10.1021/ja982520o
Sase, Shohei; Jaric, Milica; Metzger, Albrecht; Malakhov, Vladimir; Knochel, Paul (19 de setembro de 2008). «One-Pot Negishi Cross-Coupling Reactions of In Situ Generated Zinc Reagents with Aryl Chlorides, Bromides, and Triflates». The Journal of Organic Chemistry (em inglês). 73 (18): 7380–7382. ISSN 0022-3263. PMID 18693766. doi:10.1021/jo801063c

doi.org

Negishi, Eiichi; King, Anthony O.; Okukado, Nobuhisa (1 de maio de 1977). «Selective carbon-carbon bond formation via transition metal catalysis. 3. A highly selective synthesis of unsymmetrical biaryls and diarylmethanes by the nickel- or palladium-catalyzed reaction of aryl- and benzylzinc derivatives with aryl halides». The Journal of Organic Chemistry. 42 (10): 1821–1823. ISSN 0022-3263. doi:10.1021/jo00430a041
Gavryushin, Andrei; Kofink, Christiane; Manolikakes, Georg; Knochel, Paul (1 de outubro de 2005). «Efficient Cross-Coupling of Functionalized Arylzinc Halides Catalyzed by a Nickel Chloride−Diethyl Phosphite System». Organic Letters. 7 (22): 4871–4874. ISSN 1523-7060. PMID 16235910. doi:10.1021/ol051615+
Schley, Nathan D.; Fu, Gregory C. (26 de novembro de 2014). «Nickel-Catalyzed Negishi Arylations of Propargylic Bromides: A Mechanistic Investigation». Journal of the American Chemical Society. 136 (47): 16588–16593. ISSN 0002-7863. PMC 4277758. PMID 25402209. doi:10.1021/ja508718m
Morrell, Dennis G.; Kochi, Jay K. (1 de dezembro de 1975). «Mechanistic studies of nickel catalysis in the cross coupling of aryl halides with alkylmetals. Role of arylalkylnickel(II) species as intermediates». Journal of the American Chemical Society. 97 (25): 7262–7270. ISSN 0002-7863. doi:10.1021/ja00858a011
Jensen, Anne Eeg; Knochel, Paul (1 de janeiro de 2002). «Nickel-Catalyzed Cross-Coupling between Functionalized Primary or Secondary Alkylzinc Halides and Primary Alkyl Halides». The Journal of Organic Chemistry. 67 (1): 79–85. ISSN 0022-3263. PMID 11777442. doi:10.1021/jo0105787
Giovannini, Riccardo; Knochel, Paul (1 de novembro de 1998). «Ni(II)-Catalyzed Cross-Coupling between Polyfunctional Arylzinc Derivatives and Primary Alkyl Iodides». Journal of the American Chemical Society. 120 (43): 11186–11187. ISSN 0002-7863. doi:10.1021/ja982520o

harvard.edu

faculty.chemistry.harvard.edu

Andrew G Myers Research Group. «Chemistry 115 Handouts». Boston, Massachusetts: Harvard University Department of Chemistry

nih.gov

ncbi.nlm.nih.gov

Zhou, Jianrong (Steve); Fu, Gregory C. (dezembro de 2003). «Cross-Couplings of Unactivated Secondary Alkyl Halides: Room-Temperature Nickel-Catalyzed Negishi Reactions of Alkyl Bromides and Iodides». Journal of the American Chemical Society (em inglês). 125 (48): 14726–14727. ISSN 0002-7863. PMID 14640646. doi:10.1021/ja0389366
Gavryushin, Andrei; Kofink, Christiane; Manolikakes, Georg; Knochel, Paul (1 de outubro de 2005). «Efficient Cross-Coupling of Functionalized Arylzinc Halides Catalyzed by a Nickel Chloride−Diethyl Phosphite System». Organic Letters. 7 (22): 4871–4874. ISSN 1523-7060. PMID 16235910. doi:10.1021/ol051615+
McCann LC, Hunter HN, Clyburne JA, Organ MG (julho de 2012). «Higher-order zincates as transmetalators in alkyl-alkyl negishi cross-coupling». Angewandte Chemie. 51 (28): 7024–7. PMID 22685029. doi:10.1002/anie.201203547
García-Melchor M, Braga AA, Lledós A, Ujaque G, Maseras F (novembro de 2013). «Computational perspective on Pd-catalyzed C-C cross-coupling reaction mechanisms». Accounts of Chemical Research. 46 (11): 2626–34. PMID 23848308. doi:10.1021/ar400080r
Casares JA, Espinet P, Fuentes B, Salas G (março de 2007). «Insights into the mechanism of the Negishi reaction: ZnRX versus ZnR2 reagents». Journal of the American Chemical Society. 129 (12): 3508–9. PMID 17328551. doi:10.1021/ja070235b
Fuentes B, García-Melchor M, Lledós A, Maseras F, Casares JA, Ujaque G, Espinet P (agosto de 2010). «Palladium round trip in the Negishi coupling of trans-[PdMeCl(PMePh2)2] with ZnMeCl: an experimental and DFT study of the transmetalation step». Chemistry. 16 (29): 8596–9. PMID 20623568. doi:10.1002/chem.201001332
Liu Q, Lan Y, Liu J, Li G, Wu YD, Lei A (julho de 2009). «Revealing a second transmetalation step in the Negishi coupling and its competition with reductive elimination: improvement in the interpretation of the mechanism of biaryl syntheses». Journal of the American Chemical Society. 131 (29): 10201–10. PMID 19572717. doi:10.1021/ja903277d
Phapale, Vilas B.; Cárdenas, Diego J. (27 de maio de 2009). «Nickel-catalysed Negishi cross-coupling reactions: scope and mechanisms». Chemical Society Reviews (em inglês). 38 (6): 1598–1607. ISSN 1460-4744. PMID 19587955. doi:10.1039/B805648J
Schley, Nathan D.; Fu, Gregory C. (26 de novembro de 2014). «Nickel-Catalyzed Negishi Arylations of Propargylic Bromides: A Mechanistic Investigation». Journal of the American Chemical Society. 136 (47): 16588–16593. ISSN 0002-7863. PMC 4277758. PMID 25402209. doi:10.1021/ja508718m
Yu Y, Bond AD, Leonard PW, Lorenz UJ, Timofeeva TV, Vollhardt KP, Whitener GD, Yakovenko AA (junho de 2006). «Hexaferrocenylbenzene». Chemical Communications (24): 2572–4. PMID 16779481. doi:10.1039/b604844g
Zhao Y, Wang H, Hou X, Hu Y, Lei A, Zhang H, Zhu L (novembro de 2006). «Oxidative cross-coupling through double transmetallation: surprisingly high selectivity for palladium-catalyzed cross-coupling of alkylzinc and alkynylstannanes». Journal of the American Chemical Society. 128 (47): 15048–9. PMID 17117830. doi:10.1021/ja0647351
Yang Y, Oldenhuis NJ, Buchwald SL (janeiro de 2013). «Mild and general conditions for negishi cross-coupling enabled by the use of palladacycle precatalysts». Angewandte Chemie. 52 (2): 615–9. PMC 3697109. PMID 23172689. doi:10.1002/anie.201207750
Giovannini, Riccardo; Stüdemann, Thomas; Dussin, Gaelle; Knochel, Paul (1998). «An Efficient Nickel-Catalyzed Cross-Coupling Between sp3 Carbon Centers». Angewandte Chemie International Edition (em inglês). 37 (17): 2387–2390. ISSN 1521-3773. PMID 29710957. doi:10.1002/(SICI)1521-3773(19980918)37:17<2387::AID-ANIE2387>3.0.CO;2-M
Jensen, Anne Eeg; Knochel, Paul (1 de janeiro de 2002). «Nickel-Catalyzed Cross-Coupling between Functionalized Primary or Secondary Alkylzinc Halides and Primary Alkyl Halides». The Journal of Organic Chemistry. 67 (1): 79–85. ISSN 0022-3263. PMID 11777442. doi:10.1021/jo0105787
Fischer, Christian; Fu, Gregory C. (abril de 2005). «Asymmetric Nickel-Catalyzed Negishi Cross-Couplings of Secondary α-Bromo Amides with Organozinc Reagents». Journal of the American Chemical Society (em inglês). 127 (13): 4594–4595. ISSN 0002-7863. PMID 15796523. doi:10.1021/ja0506509
Son, Sunghee; Fu, Gregory C. (1 de março de 2008). «Nickel-Catalyzed Asymmetric Negishi Cross-Couplings of Secondary Allylic Chlorides with Alkylzincs». Journal of the American Chemical Society (em inglês). 130 (9): 2756–2757. ISSN 0002-7863. PMID 18257579. doi:10.1021/ja800103z
Phapale, Vilas B.; Buñuel, Elena; García-Iglesias, Miguel; Cárdenas, Diego J. (2007). «Ni-Catalyzed Cascade Formation of C(sp3)C(sp3) Bonds by Cyclization and Cross-Coupling Reactions of Iodoalkanes with Alkyl Zinc Halides». Angewandte Chemie International Edition. 46 (46): 8790–8795. ISSN 1521-3773. PMID 17918274. doi:10.1002/anie.200702528
Johansson Seechurn CC, Kitching MO, Colacot TJ, Snieckus V (maio de 2012). «Palladium-catalyzed cross-coupling: a historical contextual perspective to the 2010 Nobel Prize». Angewandte Chemie. 51 (21): 5062–85. PMID 22573393. doi:10.1002/anie.201107017
Sase S, Jaric M, Metzger A, Malakhov V, Knochel P (setembro de 2008). «One-pot Negishi cross-coupling reactions of in situ generated zinc reagents with aryl chlorides, bromides, and triflates». The Journal of Organic Chemistry. 73 (18): 7380–2. PMID 18693766. doi:10.1021/jo801063c
Nicolaou KC, Bulger PG, Sarlah D (julho de 2005). «Palladium-catalyzed cross-coupling reactions in total synthesis». Angewandte Chemie. 44 (29): 4442–89. PMID 15991198. doi:10.1002/anie.200500368
Torssell S, Wanngren E, Somfai P (maio de 2007). «Total synthesis of (-)-stemoamide». The Journal of Organic Chemistry. 72 (11): 4246–9. PMID 17451274. doi:10.1021/jo070498o
Gusovsky F, Padgett WL, Creveling CR, Daly JW (dezembro de 1992). «Interaction of pumiliotoxin B with an "alkaloid-binding domain" on the voltage-dependent sodium channel». Molecular Pharmacology. 42 (6): 1104–8. PMID 1336116
Aoyagi S, Hirashima S, Saito K, Kibayashi C (2002). «Convergent Approach to Pumiliotoxin Alkaloids. Asymmetric Total Synthesis of (+)-Pumiliotoxins A, B, and 225F». The Journal of Organic Chemistry. 67 (16): 5517–5526. PMID 12153249. doi:10.1021/jo0200466
Maloney DJ, Hecht SM (setembro de 2005). «A stereocontrolled synthesis of delta-trans-tocotrienoloic acid». Organic Letters. 7 (19): 4297–300. PMID 16146411. doi:10.1021/ol051849t
Smith, Sean W.; Fu, Gregory C. (2008). «Nickel-Catalyzed Negishi Cross-Couplings of Secondary Nucleophiles with Secondary Propargylic Electrophiles at Room Temperature». Angewandte Chemie International Edition. 47 (48): 9334–9336. ISSN 1521-3773. PMC 2790060. PMID 18972493. doi:10.1002/anie.200802784
Schmidt, Thomas; Kirschning, Andreas (2012). «Total Synthesis of Carolacton, a Highly Potent Biofilm Inhibitor». Angewandte Chemie International Edition. 51 (4): 1063–1066. ISSN 1521-3773. PMID 22162345. doi:10.1002/anie.201106762
Huo S (fevereiro de 2003). «Highly efficient, general procedure for the preparation of alkylzinc reagents from unactivated alkyl bromides and chlorides». Organic Letters. 5 (4): 423–5. PMID 12583734. doi:10.1021/ol0272693
Sase, Shohei; Jaric, Milica; Metzger, Albrecht; Malakhov, Vladimir; Knochel, Paul (19 de setembro de 2008). «One-Pot Negishi Cross-Coupling Reactions of In Situ Generated Zinc Reagents with Aryl Chlorides, Bromides, and Triflates». The Journal of Organic Chemistry (em inglês). 73 (18): 7380–7382. ISSN 0022-3263. PMID 18693766. doi:10.1021/jo801063c

orgsyn.org

Adam P. Smith, Scott A. Savage, J. Christopher Love, and Cassandra L. Fraser (2004). «Synthesis of 4-, 5-, and 6-methyl-2,2'-bipyridine by a Negishi cross-coupling strategy: 5-methyl-2,2'-bipyridine». Org. Synth. ; Coll. Vol., 10
Ei-ichi Negishi, Tamotsu Takahashi, and Anthony O. King (1993). «Synthesis of biaryls via palladium-catalyzed cross-coupling: 2-methyl-4'-nitrobiphenyl». Org. Synth. ; Coll. Vol., 8
Ei-ichi Negishi, Tamotsu Takahashi, and Shigeru Baba (1993). «Palladium-catalyzed synthesis of conjugated dienes». Org. Synth. ; Coll. Vol., 8

rsc.org

pubs.rsc.org

Phapale, Vilas B.; Cárdenas, Diego J. (27 de maio de 2009). «Nickel-catalysed Negishi cross-coupling reactions: scope and mechanisms». Chemical Society Reviews (em inglês). 38 (6): 1598–1607. ISSN 1460-4744. PMID 19587955. doi:10.1039/B805648J

wiley.com

onlinelibrary.wiley.com

Giovannini, Riccardo; Stüdemann, Thomas; Dussin, Gaelle; Knochel, Paul (1998). «An Efficient Nickel-Catalyzed Cross-Coupling Between sp3 Carbon Centers». Angewandte Chemie International Edition (em inglês). 37 (17): 2387–2390. ISSN 1521-3773. PMID 29710957. doi:10.1002/(SICI)1521-3773(19980918)37:17<2387::AID-ANIE2387>3.0.CO;2-M
Phapale, Vilas B.; Buñuel, Elena; García-Iglesias, Miguel; Cárdenas, Diego J. (2007). «Ni-Catalyzed Cascade Formation of C(sp3)C(sp3) Bonds by Cyclization and Cross-Coupling Reactions of Iodoalkanes with Alkyl Zinc Halides». Angewandte Chemie International Edition. 46 (46): 8790–8795. ISSN 1521-3773. PMID 17918274. doi:10.1002/anie.200702528
Smith, Sean W.; Fu, Gregory C. (2008). «Nickel-Catalyzed Negishi Cross-Couplings of Secondary Nucleophiles with Secondary Propargylic Electrophiles at Room Temperature». Angewandte Chemie International Edition. 47 (48): 9334–9336. ISSN 1521-3773. PMC 2790060. PMID 18972493. doi:10.1002/anie.200802784
Schmidt, Thomas; Kirschning, Andreas (2012). «Total Synthesis of Carolacton, a Highly Potent Biofilm Inhibitor». Angewandte Chemie International Edition. 51 (4): 1063–1066. ISSN 1521-3773. PMID 22162345. doi:10.1002/anie.201106762

worldcat.org

Zhou, Jianrong (Steve); Fu, Gregory C. (dezembro de 2003). «Cross-Couplings of Unactivated Secondary Alkyl Halides: Room-Temperature Nickel-Catalyzed Negishi Reactions of Alkyl Bromides and Iodides». Journal of the American Chemical Society (em inglês). 125 (48): 14726–14727. ISSN 0002-7863. PMID 14640646. doi:10.1021/ja0389366
Negishi, Eiichi; King, Anthony O.; Okukado, Nobuhisa (1 de maio de 1977). «Selective carbon-carbon bond formation via transition metal catalysis. 3. A highly selective synthesis of unsymmetrical biaryls and diarylmethanes by the nickel- or palladium-catalyzed reaction of aryl- and benzylzinc derivatives with aryl halides». The Journal of Organic Chemistry. 42 (10): 1821–1823. ISSN 0022-3263. doi:10.1021/jo00430a041
Gavryushin, Andrei; Kofink, Christiane; Manolikakes, Georg; Knochel, Paul (1 de outubro de 2005). «Efficient Cross-Coupling of Functionalized Arylzinc Halides Catalyzed by a Nickel Chloride−Diethyl Phosphite System». Organic Letters. 7 (22): 4871–4874. ISSN 1523-7060. PMID 16235910. doi:10.1021/ol051615+
Phapale, Vilas B.; Cárdenas, Diego J. (27 de maio de 2009). «Nickel-catalysed Negishi cross-coupling reactions: scope and mechanisms». Chemical Society Reviews (em inglês). 38 (6): 1598–1607. ISSN 1460-4744. PMID 19587955. doi:10.1039/B805648J
Schley, Nathan D.; Fu, Gregory C. (26 de novembro de 2014). «Nickel-Catalyzed Negishi Arylations of Propargylic Bromides: A Mechanistic Investigation». Journal of the American Chemical Society. 136 (47): 16588–16593. ISSN 0002-7863. PMC 4277758. PMID 25402209. doi:10.1021/ja508718m
Morrell, Dennis G.; Kochi, Jay K. (1 de dezembro de 1975). «Mechanistic studies of nickel catalysis in the cross coupling of aryl halides with alkylmetals. Role of arylalkylnickel(II) species as intermediates». Journal of the American Chemical Society. 97 (25): 7262–7270. ISSN 0002-7863. doi:10.1021/ja00858a011
Giovannini, Riccardo; Stüdemann, Thomas; Dussin, Gaelle; Knochel, Paul (1998). «An Efficient Nickel-Catalyzed Cross-Coupling Between sp3 Carbon Centers». Angewandte Chemie International Edition (em inglês). 37 (17): 2387–2390. ISSN 1521-3773. PMID 29710957. doi:10.1002/(SICI)1521-3773(19980918)37:17<2387::AID-ANIE2387>3.0.CO;2-M
Jensen, Anne Eeg; Knochel, Paul (1 de janeiro de 2002). «Nickel-Catalyzed Cross-Coupling between Functionalized Primary or Secondary Alkylzinc Halides and Primary Alkyl Halides». The Journal of Organic Chemistry. 67 (1): 79–85. ISSN 0022-3263. PMID 11777442. doi:10.1021/jo0105787
Giovannini, Riccardo; Knochel, Paul (1 de novembro de 1998). «Ni(II)-Catalyzed Cross-Coupling between Polyfunctional Arylzinc Derivatives and Primary Alkyl Iodides». Journal of the American Chemical Society. 120 (43): 11186–11187. ISSN 0002-7863. doi:10.1021/ja982520o
Fischer, Christian; Fu, Gregory C. (abril de 2005). «Asymmetric Nickel-Catalyzed Negishi Cross-Couplings of Secondary α-Bromo Amides with Organozinc Reagents». Journal of the American Chemical Society (em inglês). 127 (13): 4594–4595. ISSN 0002-7863. PMID 15796523. doi:10.1021/ja0506509
Son, Sunghee; Fu, Gregory C. (1 de março de 2008). «Nickel-Catalyzed Asymmetric Negishi Cross-Couplings of Secondary Allylic Chlorides with Alkylzincs». Journal of the American Chemical Society (em inglês). 130 (9): 2756–2757. ISSN 0002-7863. PMID 18257579. doi:10.1021/ja800103z
Phapale, Vilas B.; Buñuel, Elena; García-Iglesias, Miguel; Cárdenas, Diego J. (2007). «Ni-Catalyzed Cascade Formation of C(sp3)C(sp3) Bonds by Cyclization and Cross-Coupling Reactions of Iodoalkanes with Alkyl Zinc Halides». Angewandte Chemie International Edition. 46 (46): 8790–8795. ISSN 1521-3773. PMID 17918274. doi:10.1002/anie.200702528
Smith, Sean W.; Fu, Gregory C. (2008). «Nickel-Catalyzed Negishi Cross-Couplings of Secondary Nucleophiles with Secondary Propargylic Electrophiles at Room Temperature». Angewandte Chemie International Edition. 47 (48): 9334–9336. ISSN 1521-3773. PMC 2790060. PMID 18972493. doi:10.1002/anie.200802784
Schmidt, Thomas; Kirschning, Andreas (2012). «Total Synthesis of Carolacton, a Highly Potent Biofilm Inhibitor». Angewandte Chemie International Edition. 51 (4): 1063–1066. ISSN 1521-3773. PMID 22162345. doi:10.1002/anie.201106762
Sase, Shohei; Jaric, Milica; Metzger, Albrecht; Malakhov, Vladimir; Knochel, Paul (19 de setembro de 2008). «One-Pot Negishi Cross-Coupling Reactions of In Situ Generated Zinc Reagents with Aryl Chlorides, Bromides, and Triflates». The Journal of Organic Chemistry (em inglês). 73 (18): 7380–7382. ISSN 0022-3263. PMID 18693766. doi:10.1021/jo801063c

zenodo.org

Yu Y, Bond AD, Leonard PW, Lorenz UJ, Timofeeva TV, Vollhardt KP, Whitener GD, Yakovenko AA (junho de 2006). «Hexaferrocenylbenzene». Chemical Communications (24): 2572–4. PMID 16779481. doi:10.1039/b604844g