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Kinetic resolution (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Kinetic resolution" in English language version.

refsWebsite
Global rank English rank
55doi.org
2nd place
2nd place
21nih.gov
4th place
4th place
15harvard.edu
18th place
17th place
1zenodo.org
621st place
380th place
1espacenet.com
800th place
676th place
1rero.ch
3,510th place
2,263rd place
1semanticscholar.org
11th place
8th place
1handle.net
102nd place
76th place

doi.org (Global: 2nd place; English: 2nd place)

  • Robinson, D.E.J.E.; Bull, S.D. (2005). "Kinetic resolution strategies using non-enzymatic catalysts". Tetrahedron: Asymmetry. 14 (11): 1407–1446. doi:10.1016/S0957-4166(03)00209-X.
  • Marckwald, W.; McKenzie, A. (1899). "Ueber eine principiell neue Methode zur Spaltung racemischer Verbindungen in die activen Bestandtheile". Ber. Dtsch. Chem. Ges. 32 (2): 2130–2136. doi:10.1002/cber.189903202130.
  • Roger, R.; Read, J. (1952). "Alexander McKenzie: 1869-1951". Obituary Notices of Fellows of the Royal Society. 8 (21): 206–228. doi:10.1098/rsbm.1952.0014.
  • Keith, J. M.; Larrow, J. F.; Jacobsen, E. N. (2001). "Practical Considerations in Kinetic Resolution Reactions". Adv. Synth. Catal. 343: 5–26. doi:10.1002/1615-4169(20010129)343:1<5::AID-ADSC5>3.0.CO;2-I.
  • Wurz, R.P.; Lee, E.C.; Ruble, J.C.; Fu, G.C. (2007). "Synthesis and Resolution of Planar-Chiral Derivatives of 4-(Dimethylamino)pyridine". Adv. Synth. Catal. 349 (14–15): 2345–2352. doi:10.1002/adsc.200700219.
  • Ruble, J.C.; Latham, H.A.; Fu, G.C. (1997). "Effective Kinetic Resolution of Secondary Alcohols with a Planar-Chiral Analogue of 4-(Dimethylamino)pyridine. Use of the Fe(C5Ph5) Group in Asymmetric Catalysis". J. Am. Chem. Soc. 119 (6): 1492–1493. doi:10.1021/ja963835b.
  • Ruble, J.C.; Tweddell, J.; Fu, G.C. (1998). "Kinetic Resolution of Arylakylcarbinols Catalyzed by a Planar-Chiral Derivative of DMAP: A New Benchmark for Nonenzymatic Acylation". J. Org. Chem. 63 (9): 2794–2795. doi:10.1021/jo980183w.
  • Tao, B.; Ruble, J.C.; Hoic, D.A.; Fu, G.C. (1999). "Nonenzymatic Kinetic Resolution of Propargylic Alcohols by a Planar−Chiral DMAP Derivative: Crystallographic Characterization of the Acylated Catalyst". J. Am. Chem. Soc. 121 (21): 2091–5092. Bibcode:1999JAChS.121.5091T. doi:10.1021/ja9906958.
  • Bellemin-Laponnaz, S.; Tweddell, J.; Ruble, J.C.; Breitling, F.M.; Fu, G.C. (2000). "The kinetic resolution of allylic alcohols by a non-enzymatic acylation catalyst; application to natural product synthesis". Chem. Commun. (12): 2091–5092. doi:10.1039/B002041I.
  • Arai, S.; Bellemin-Laponnaz, S.; Fu, G.C. (2001). "Kinetic Resolution of Amines by a Nonenzymatic Acylation Catalyst". Angew. Chem. Int. Ed. 133 (1): 240–242. Bibcode:2001AngCh.113..240A. doi:10.1002/1521-3757(20010105)113:1<240::AID-ANGE240>3.0.CO;2-E.
  • Arp, F.O.; Fu, G.C. (2006). "Kinetic Resolutions of Inolines by a Nonenzymatic Acylation Catalyst". J. Am. Chem. Soc. 128 (44): 14264–14265. Bibcode:2006JAChS.12814264A. doi:10.1021/ja0657859. PMC 2569996. PMID 17076493.
  • Katsuki, T.; Sharpless, K.B. (1980). "The first practical method for asymmetric epoxidation". J. Am. Chem. Soc. 102 (18): 5974–5976. Bibcode:1980JAChS.102.5974K. doi:10.1021/ja00538a077.
  • Martin, V.; Woodard, S.; Katsuki, T.; Yamada, Y.; Ikeda, M.; Sharpless, K.B. (1981). "Kinetic resolution of racemic allylic alcohols by enantioselective epoxidation. A route to substances of absolute enantiomeric purity?". J. Am. Chem. Soc. 103 (23): 6237–6240. Bibcode:1981JAChS.103.6237M. doi:10.1021/ja00410a053.
  • Gao, Yun; Klunder, J.M.; Hanson, R.M.; Masamune, H.; Ko, S.Y.; Sharpless, K.B. (1987). "Catalytic asymmetric epoxidation and kinetic resolution: modified procedures including in situ derivatization". J. Am. Chem. Soc. 109 (19): 5765–5780. Bibcode:1987JAChS.109.5765G. doi:10.1021/ja00253a032.
  • Kitano, Y.; Matsumoto, T.; Sato, F. (1988). "A highly efficient kinetic resolution of γ- and β- trimethylsilyl secondary allylic alcohols by the sharpless asymmetric epoxidation". Tetrahedron. 44 (13): 4073–4086. doi:10.1016/S0040-4020(01)86657-6.
  • VanNieuwenhze, M.S.; Sharpless, K.B. (1993). "Kinetic resolution of racemic olefins via asymmetric dihydroxylation". J. Am. Chem. Soc. 115 (17): 7864–7865. Bibcode:1993JAChS.115.7864V. doi:10.1021/ja00070a037.
  • Corey, E.J.; Noe, M.C.; Guzman-Perez, A. (1995). "Kinetic Resolution by Enantioselective Dihydroxylation of Secondary Allylic 4-Methoxybenzoate Esters Using a Mechanistically Designed Cinchona Alkaloid Catalyst". J. Am. Chem. Soc. 117 (44): 10817–10824. Bibcode:1995JAChS.11710817C. doi:10.1021/ja00149a004.
  • Lorenz, J.C.; Frohn, M.; Zhou, X.; Zhang, J.-R.; Tang, Y.; Burke, C.; Shi, Y. (2005). "Transition State Studies on the Dioxirane-Mediated Asymmetric Epoxidation via Kinetic Resolution and Desymmetrization". J. Org. Chem. 70 (8): 2904–2911. doi:10.1021/jo048217p. PMID 15822948.
  • Larrow, J.F.; Schaus, S.E.; Jacobsen, E.N. (1996). "Kinetic Resolution of Terminal Epoxides via Highly Regioselective and Enantioselective Ring Opening with TMSN3. An Efficient, Catalytic Route to 1,2-Amino Alcohols". J. Am. Chem. Soc. 118 (31): 7420–7421. Bibcode:1996JAChS.118.7420L. doi:10.1021/ja961708+.
  • Tokunaga, M.; Larrow, J.F.; Kakiuchi, F.; Jacobsen, E.N. (1997). "Asymmetric Catalysis with Water: Efficient Kinetic Resolution of Terminal Epoxides by Means of Catalytic Hydrolysis". Science. 277 (5328): 936–938. doi:10.1126/science.277.5328.936. PMID 9252321.
  • Brandes, B.D.; Jacobsen, E.N. (1997). "Synthesis of enantiopure 3-chlorostyrene oxide via an asymmetric epoxidation-hydrolytic kinetic resolution sequence". Tet. Asymm. 8 (23): 3927–3933. doi:10.1016/S0957-4166(97)00568-5.
  • Sudalai, A.; Karabal, P.U.; Devalankar, D.A. (2013). "Optically pure γ-butyrolactones and epoxy esters via two stereocentered HKR of 3-substituted epoxy esters: a formal synthesis of (−)-paroxetine, Ro 67-8867 and(+)-eldanolide". Org. Biomol. Chem. 11 (8): 1280–1285. doi:10.1039/c3ob27321k. PMID 23334653.
  • Hashiguchi, S.; Fujii, A.; Haack, K.-J.; Matsumura, K.; Ikariya, T.; Noyori, R. (1997). "Kinetic Resolution of Racemic Secondary Alcohols by RuII-Catalyzed Hydrogen Transfer". Angew. Chem. Int. Ed. 36 (3): 288–290. doi:10.1002/anie.199702881.
  • Hashiguchi, S.; Fujii, A.; Takehara, J.; Ikariya, T.; Noyori, R. (1995). "Asymmetric Transfer Hydrogenation of Aromatic Ketones Catalyzed by Chiral Ruthenium(II) Complexes". J. Am. Chem. Soc. 117 (28): 7562–7563. Bibcode:1995JAChS.117.7562H. doi:10.1021/ja00133a037.
  • Nishibayashi, Y.; Takei, I.; Uemura, S.; Hidai, M. (1999). "Extremely High Enantioselective Redox Reaction of Ketones and Alcohols Catalyzed by RuCl2(PPh3)(oxazolinylferrocenylphosphine)". Organometallics. 18 (12): 2291–2293. doi:10.1021/om990210o.
  • Kitamura, M.; Kasahara, I.; Manabe, K.; Noyori, R.; Takaya, H. (1988). "Kinetic resolution of racemic allylic alcohols by BINAP-ruthenium(II) catalyzed hydrogenation". J. Org. Chem. 53 (3): 708–710. doi:10.1021/jo00238a048.
  • Hoveyda, A.H.; Schrock, R.R. (2001). "Catalytic Asymmetric Olefin Metathesis". Chem. Eur. J. 7 (5): 945–950. doi:10.1002/1521-3765(20010302)7:5<945::AID-CHEM945>3.0.CO;2-3. PMID 11303874.
  • Ghanem, A.; Aboul-Enein, H.Y. (2005). "Application of lipases in kinetic resolution of racemates". Chirality. 17 (1): 1–15. doi:10.1002/chir.20089. PMID 15515046.
  • Ghanem, A.; Schurig, V. (2003). "Lipase-catalyzed Irreversible Transesterification of Secondary Alcohols Using Isopropenyl Acetate" (PDF). Monatshefte für Chemie. 134 (8): 1151–1157. doi:10.1007/s00706-003-0025-1. S2CID 96922176.
  • Santaniello, E.; Ferraboschi, P.; Grisenti, P.; Manzocchi, A. (1992). "The biocatalytic approach to the preparation of enantiomerically pure chiral building blocks". Chem. Rev. 92 (5): 1071–1140. doi:10.1021/cr00013a016.
  • Ticozzi, C.; Zanarotti, Antonio (1989). "Enantioselective Microbial Reduction of 5-Acetylisoxazolines – A Novel Method for Stereochemical Control on Yeast Reduction". Liebigs Ann. Chem. 1989 (12): 1257–1259. doi:10.1002/jlac.198919890299.
  • Fantin, G.; Fogagnolo, M.; Medici, A.; Pedrini, P.; Poli, S. (1993). "Kinetic resolution of 1-aryl- and 1-heteroaryl ethanols by oxidation with Baker's yeast". Tetrahedron Lett. 34 (5): 883–884. doi:10.1016/0040-4039(93)89039-S. hdl:11392/462444.
  • Brooks, D.W.; Wilson, M.; Webb, M. (1987). "Different enzymic reactions of an enantiomeric pair: simultaneous dual kinetic resolution of a keto ester by bakers' yeast". J. Org. Chem. 52 (11): 2244–2248. doi:10.1021/jo00387a026.
  • Pellissier, H. (2008). "Recent developments in dynamic kinetic resolution". Tetrahedron. 64 (8): 1563–1601. doi:10.1016/j.tet.2007.10.080.
  • Pellissier, H. (2003). "Dynamic kinetic resolution". Tetrahedron. 59 (42): 8291–8327. doi:10.1016/S0040-4020(03)01022-6.
  • Ward, R.S. (1995). "Dynamic kinetic resolution". Tetrahedron: Asymmetry. 6 (7): 1475–1490. doi:10.1016/0957-4166(95)00179-S.
  • Kitamura, M.; Tokunaga, M.; Noyori, R. (1993). "Quantitative expression of dynamic kinetic resolution of chirally labile enantiomers: stereoselective hydrogenation of 2-substituted 3-oxo carboxylic esters catalyzed by BINAP-ruthenium(II) complexes". J. Am. Chem. Soc. 115 (1): 144–152. Bibcode:1993JAChS.115..144K. doi:10.1021/ja00054a020.
  • Noyori, R.; Ikeda, T.; Ohkuma, T.; Widhalm, M.; Kitamura, M.; Takaya, H.; Akutagawa, S.; Sayo, N.; Saito, T. (1989). "Stereoselective hydrogenation via dynamic kinetic resolution". J. Am. Chem. Soc. 111 (25): 9134–9135. Bibcode:1989JAChS.111.9134N. doi:10.1021/ja00207a038.
  • de Paule, S.D.; Jeulin, S.; Ratovelomanana-Vidal, V.; Genêt, J-P.; Champion, N.; Dellis, P. (2003). "Synthesis and Molecular Modeling Studies of SYNPHOS®, a New, Efficient Diphosphane Ligand For Ruthenium-Catalyzed Asymmetric Hydrogenation". Eur. J. Org. Chem. 2003 (10): 1931–1941. doi:10.1002/ejoc.200200634.
  • Mordant, C.; Ratovelomanana-Vidal, V.; Dünkelmann, P.; Genêt, J.-P. (2004). "A Versatile Route to syn- and anti-α-Amino β-Hydroxy Esters from β-Keto Esters by Dynamic Kinetic Resolution with Ru-SYNPHOS® Catalyst". Eur. J. Org. Chem. 2004 (14): 3017–3026. doi:10.1002/ejoc.200400078.
  • Lee, S.Y.; Murphy, J.M.; Ukai, A.; Fu, G.C. (2012). "Nonenzymatic Dynamic Kinetic Resolution of Secondary Alcohols via Enantioselective Acylation: Synthetic and Mechanistic Studies". J. Am. Chem. Soc. 134 (36): 15149–15153. Bibcode:2012JAChS.13415149L. doi:10.1021/ja307425g. PMC 3447740. PMID 22934603.
  • Pellissier, H. (2003). "Lipase–triethylamine-mediated dynamic transesterification of a tricyclic acyloin having a latent meso-structure: a new route to optically pure oxodicyclopentadiene". Tetrahedron. 59 (42): 8291–9327. doi:10.1016/S0040-4020(03)01022-6.
  • Taniguchi, T.; Ogasawara, K. (1997). "Lipase–triethylamine-mediated dynamic transesterification of a tricyclic acyloin having a latent meso-structure: a new route to optically pure oxodicyclopentadiene". Chemical Communications (15): 1399–1400. doi:10.1039/A702910A.
  • Crawford, J.B.; Skerlj, R.T.; Bridger, G.J. (2007). "Spontaneous Enzymatically Mediated Dynamic Kinetic Resolution of 8-Amino-5,6,7,8-tetrahydroquinoline". J. Org. Chem. 72 (2): 669–671. doi:10.1021/jo062037t. PMID 17221995.
  • Pàmies, O.; Bäckvall, J.-E. (2004). "Chemoenzymatic dynamic kinetic resolution". Trends in Biotechnology. 22 (3): 130–135. doi:10.1016/j.tibtech.2004.01.005. PMID 15036863.
  • Pàmies, O.; Bäckvall, J.-E. (2002). "Enzymatic Kinetic Resolution and Chemoenzymatic Dynamic Kinetic Resolution of δ-Hydroxy Esters. An Efficient Route to Chiral δ-Lactones". J. Org. Chem. 67 (4): 1261–1265. doi:10.1021/jo016096c. PMID 11846671.
  • Martín-Matute, B.; Edin, M.; Bogár, K.; Kaynak, F.B.; Bäckvall, J.-E. (2005). "Combined Ruthenium(II) and Lipase Catalysis for Efficient Dynamic Kinetic Resolution of Secondary Alcohols. Insight into the Racemization Mechanism". J. Am. Chem. Soc. 127 (64): 8817–8825. Bibcode:2005JAChS.127.8817M. doi:10.1021/ja051576x. PMID 15954789.
  • Choi, Y.K.; Suh, J.H.; Lee, D.; Lim, I.T.; Jung, J.Y.; Kim, M.-J. (1999). "Dynamic Kinetic Resolution of Acyclic Allylic Acetates Using Lipase and Palladium". J. Org. Chem. 64 (22): 8423–8424. doi:10.1021/jo990956w. PMID 11674772.
  • Lee, D.; Huh, E.A.; Kim, M.-J.; Jung, H.M.; Koh, J.H.; Park, J. (2000). "Dynamic Kinetic Resolution of Allylic Alcohols Mediated by Ruthenium- and Lipase-Based Catalysts". Org. Lett. 2 (15): 2377–2379. doi:10.1021/ol006159y. PMID 10930288.
  • Eames, J. (2000). "Parallel Kinetic Resolutions". Angew. Chem. Int. Ed. 39 (5): 885–888. doi:10.1002/(SICI)1521-3773(20000303)39:5<885::AID-ANIE885>3.0.CO;2-2. PMID 10760881.
  • Dehil, J.R.; Gotor, V. (2002). "Parallel kinetic resolution of racemic mixtures: a new strategy for the preparation of enantiopure compounds?". Chem. Soc. Rev. 31 (6): 365–370. doi:10.1039/B205280F. PMID 12491751.
  • Vedejs, E.; Jure, M. (2005). "Efficiency in Nonenzymatic Kinetic Resolution". Angew. Chem. Int. Ed. 44 (5): 3974–4001. doi:10.1002/anie.200460842. PMID 15942973.
  • Kurosu, M.; Kishi, Y. (1998). "A Novel Example for Optical Resolution of Racemic Ketones Originating from Batrachotoxin Synthesis". J. Org. Chem. 63 (18): 6100–6101. doi:10.1021/jo981416m. PMID 11672234.
  • Dehil, J.R.; Gotor, V. (2002). "Preparation of Enantiopure Ketones and Alcohols Containing a Quaternary Stereocenter through Parallel Kinetic Resolution of β-Keto Nitriles". J. Org. Chem. 67 (5): 1716–1718. doi:10.1021/jo011092t. PMID 11871913.
  • Tanaka, K.; Fu, G.C. (2003). "Parallel Kinetic Resolution of 4-Alkynals Catalyzed by Rh(I)/Tol-BINAP: Synthesis of Enantioenriched Cyclobutanones and Cyclopentenones". J. Am. Chem. Soc. 125 (27): 8078–8079. Bibcode:2003JAChS.125.8078T. doi:10.1021/ja035489l. PMID 12837058.

espacenet.com (Global: 800th place; English: 676th place)

worldwide.espacenet.com

  • US patent 6656710, Bommarius & Verseck, "Process for the production of amino acids using racemase and Acylate", assigned to Degussa AG 

handle.net (Global: 102nd place; English: 76th place)

hdl.handle.net

  • Fantin, G.; Fogagnolo, M.; Medici, A.; Pedrini, P.; Poli, S. (1993). "Kinetic resolution of 1-aryl- and 1-heteroaryl ethanols by oxidation with Baker's yeast". Tetrahedron Lett. 34 (5): 883–884. doi:10.1016/0040-4039(93)89039-S. hdl:11392/462444.

harvard.edu (Global: 18th place; English: 17th place)

ui.adsabs.harvard.edu

nih.gov (Global: 4th place; English: 4th place)

pubmed.ncbi.nlm.nih.gov

ncbi.nlm.nih.gov

rero.ch (Global: 3,510th place; English: 2,263rd place)

doc.rero.ch

semanticscholar.org (Global: 11th place; English: 8th place)

api.semanticscholar.org

zenodo.org (Global: 621st place; English: 380th place)