Michael addition reaction (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Michael addition reaction" in English language version.

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29doi.org

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8nih.gov

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7worldcat.org

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4semanticscholar.org

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3harvard.edu

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3sciencedirect.com

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1elsevier.com

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acs.org

pubs.acs.org

Huang, Sijia; Sinha, Jasmine; Podgórski, Maciej; Zhang, Xinpeng; Claudino, Mauro; Bowman, Christopher N. (14 August 2018). "Mechanistic Modeling of the Thiol–Michael Addition Polymerization Kinetics: Structural Effects of the Thiol and Vinyl Monomers". Macromolecules. 51 (15): 5979–5988. Bibcode:2018MaMol..51.5979H. doi:10.1021/acs.macromol.8b01264. ISSN 0024-9297. S2CID 105834506.
Jung, Hyuk-Joon; Yu, Insun; Nyamayaro, Kudzanai; Mehrkhodavandi, Parisa (5 June 2020). "Indium-Catalyzed Block Copolymerization of Lactide and Methyl Methacrylate by Sequential Addition". ACS Catalysis. 10 (11): 6488–6496. doi:10.1021/acscatal.0c01365. ISSN 2155-5435. S2CID 219762406.

bnf.fr

gallica.bnf.fr

Michael, A. (1887). "Ueber die Addition von Natriumacetessig- und Natriummalonsäureäthern zu den Aethern ungesättigter Säuren" [On the addition of sodium acetoacetate- and sodium malonic acid esters to the esters of unsaturated acids]. Journal für Praktische Chemie. 2nd series. 35: 349–356. doi:10.1002/prac.18870350136.
Michael, A. (1894). "Ueber die Addition von Natriumacetessig- und Natriummalonsäureäther zu den Aethern ungesättigter Säuren" [On the addition of sodium acetoacetate- and sodium malonic acid esters to the esters of unsaturated acids]. Journal für Praktische Chemie. 2nd series. 49: 20–25. doi:10.1002/prac.18940490103.

doi.org

Little, R. D.; Masjedizadeh, M. R.; Wallquist, O.; McLoughlin, J. I. (1995). "The Intramolecular Michael Reaction". Org. React. Vol. 47. pp. 315–552. doi:10.1002/0471264180.or047.02. ISBN 978-0-471-26418-7.
Mather, B.; Viswanathan, K.; Miller, K.; Long, T. (2006). "Michael addition reactions in macromolecular design for emerging technologies". Progress in Polymer Science. 31 (5): 487–531. doi:10.1016/j.progpolymsci.2006.03.001.
Tiano, Martin (2020). "Enantioselective Michael Addition: An Experimental Introduction to Asymmetric Synthesis". Journal of Chemical Education. 97 (8): 2291–2295. Bibcode:2020JChEd..97.2291T. doi:10.1021/acs.jchemed.0c00164.
Michael, A. (1887). "Ueber die Addition von Natriumacetessig- und Natriummalonsäureäthern zu den Aethern ungesättigter Säuren" [On the addition of sodium acetoacetate- and sodium malonic acid esters to the esters of unsaturated acids]. Journal für Praktische Chemie. 2nd series. 35: 349–356. doi:10.1002/prac.18870350136.
Michael, A. (1894). "Ueber die Addition von Natriumacetessig- und Natriummalonsäureäther zu den Aethern ungesättigter Säuren" [On the addition of sodium acetoacetate- and sodium malonic acid esters to the esters of unsaturated acids]. Journal für Praktische Chemie. 2nd series. 49: 20–25. doi:10.1002/prac.18940490103.
Mather, Brian D.; Viswanathan, Kalpana; Miller, Kevin M.; Long, Timothy E. (1 May 2006). "Michael addition reactions in macromolecular design for emerging technologies". Progress in Polymer Science. 31 (5): 487–531. doi:10.1016/j.progpolymsci.2006.03.001. ISSN 0079-6700.
Guin, Soumitra; Saha, Hemonta K.; Patel, Ashvani K.; Gudimella, Santosh K.; Biswas, Subhankar; Samanta, Sampak (17 July 2020). "1,6-Aza-Michael addition of para-quinone methides with N-heterocycles catalyzed by Zn(OTf)2: A regioselective approach to N-diarylmethyl-substituted heterocycles". Tetrahedron. 76 (28): 131338. doi:10.1016/j.tet.2020.131338. ISSN 0040-4020. S2CID 225589003.
Perlmutter, P., ed. (1 January 1992), "Chapter One – Introduction", Tetrahedron Organic Chemistry Series, Conjugate Addition Reactions in Organic Synthesis, vol. 9, Elsevier, pp. 1–61, doi:10.1016/b978-0-08-037067-5.50007-2, retrieved 7 October 2022
Conrad, M.; Guthzeit, M. (1884). "Ueber die Einwirkung von α-β-Dibrompropionsäure auf Malonsäureester" [On the reaction of 2,3-dibrompropionic acid with [diethyl] malonic acid ester]. Berichte der Deutschen Chemischen Gesellschaft. 17 (1): 1185–1188. doi:10.1002/cber.188401701314.
Tokoroyama, T. (2010). "Discovery of the Michael Reaction". European Journal of Organic Chemistry. 2010 (10): 2009–2016. doi:10.1002/ejoc.200901130.
Claisen, L. (1887). "Bemerkung über die Addition von Aethylmalonat an Körper mit doppelter Kohlenstoffbindung" [Observation on the addition of [di]ethyl malonate to substances with a double carbon bond]. Journal für Praktische Chemie. 2nd series. 35 (1): 413–415. doi:10.1002/prac.18870350144.
Komnenos, T. (1883). "Ueber die Einwirkung von Fettaldehyden auf Malonsäure und Aethylmalonat" [On the reaction of aliphatic aldehydes with malonic acid and [di]ethylmalonate]. Justus Liebig's Annalen der Chemie. 218 (2): 145–167. doi:10.1002/jlac.18832180204.
Reyes, E.; Uria, U.; Vicario, J. L.; Carrillo, L. (2016). "The Catalytic, Enantioselective Michael Reaction". Organic Reactions. 90: 1–898. doi:10.1002/0471264180.or090.01. ISBN 9780471264187.
Pansare, S. V.; Pandya, K. (2006). "Simple Diamine- and Triamine-Protonic Acid Catalysts for the Enantioselective Michael Addition of Cyclic Ketones to Nitroalkenes". Journal of the American Chemical Society. 128 (30): 9624–9625. doi:10.1021/ja062701n. PMID 16866504.
Ikawa, M.; Stahmann, M. A.; Link, K. P. (1944). "Studies on 4-Hydroxycoumarins. V. The Condensation of α,β-Unsaturated Ketones with 4-Hydroxycoumarin". Journal of the American Chemical Society. 66 (6): 902. doi:10.1021/ja01234a019.
Halland, N.; Hansen, T.; Jørgensen, K. (2003). "Organocatalytic asymmetric Michael reaction of cyclic 1,3-dicarbonyl compounds and α,β-unsaturated ketones--a highly atom-economic catalytic one-step formation of optically active warfarin anticoagulant". Angewandte Chemie. 42 (40): 4955–4957. doi:10.1002/anie.200352136. PMID 14579449.
Kim, H.; Yen, C.; Preston, P.; Chin, J. (2006). "Substrate-directed stereoselectivity in vicinal diamine-catalyzed synthesis of warfarin". Organic Letters. 8 (23): 5239–5242. doi:10.1021/ol062000v. PMID 17078687.
Xie, J.; Yue, L.; Chen, W.; Du, W.; Zhu, J.; Deng, J.; Chen, Y. (2007). "Highly Enantioselective Michael Addition of Cyclic 1,3-Dicarbonyl Compounds to α,β-Unsaturated Ketones". Organic Letters. 9 (3): 413–415. doi:10.1021/ol062718a. PMID 17249775.
Kristensen, T. E.; Vestli, K.; Hansen, F. K.; Hansen, T. (2009). "New Phenylglycine-Derived Primary Amine Organocatalysts for the Preparation of Optically Active Warfarin". European Journal of Organic Chemistry. 2009 (30): 5185. doi:10.1002/ejoc.200900664.
Dong, Z.; Wang, L.; Chen, X.; Liu, X.; Lin, L.; Feng, X. (2009). "Organocatalytic Enantioselective Michael Addition of 4-Hydroxycoumarin to α,β-Unsaturated Ketones: A Simple Synthesis of Warfarin". European Journal of Organic Chemistry. 2009 (30): 5192. doi:10.1002/ejoc.200900831.
Wong, T. C.; Sultana, C. M.; Vosburg, D. A. (2010). "A Green, Enantioselective Synthesis of Warfarin for the Undergraduate Organic Laboratory". Journal of Chemical Education. 87 (2): 194. Bibcode:2010JChEd..87..194W. doi:10.1021/ed800040m.
Mukaiyama, T. (1977). "Titanium Tetrachloride in Organic Synthesis [New synthetic methods (21)]". Angew. Chem. Int. Ed. Engl. 16 (12): 817–826. doi:10.1002/anie.197708171.
Lippert, A. R.; Kaeobamrung, J.; Bode, J. W. (2006). "Synthesis of Oligosubstituted Bullvalones: Shapeshifting Molecules Under Basic Conditions". Journal of the American Chemical Society. 128 (46): 14738–14739. doi:10.1021/ja063900+. PMID 17105247.
Hayashi, Yujiro; Okamura, Daichi; Umemiya, Shigenobu; Uchimaru, Tadafumi (July 2012). "Organocatalytic 1,4-Addition Reaction of α,β-γ,δ-Diunsaturated Aldehydes versus 1,6-Addition Reaction". ChemCatChem. 4 (7): 959–962. doi:10.1002/cctc.201200161. S2CID 98643888.
den Hartog, Tim; Harutyunyan, Syuzanna R.; Font, Daniel; Minnaard, Adriaan J.; Feringa, Ben L. (January 2008). "Catalytic Enantioselective 1,6-Conjugate Addition of Grignard Reagents to Linear Dienoates". Angewandte Chemie International Edition. 47 (2): 398–401. doi:10.1002/anie.200703702. PMID 18041800.
Boike, Lydia; Henning, Nathaniel J.; Nomura, Daniel K. (25 August 2022). "Advances in covalent drug discovery". Nature Reviews Drug Discovery. 21 (12): 881–898. doi:10.1038/s41573-022-00542-z. ISSN 1474-1776. PMC 9403961. PMID 36008483.
Huang, Sijia; Sinha, Jasmine; Podgórski, Maciej; Zhang, Xinpeng; Claudino, Mauro; Bowman, Christopher N. (14 August 2018). "Mechanistic Modeling of the Thiol–Michael Addition Polymerization Kinetics: Structural Effects of the Thiol and Vinyl Monomers". Macromolecules. 51 (15): 5979–5988. Bibcode:2018MaMol..51.5979H. doi:10.1021/acs.macromol.8b01264. ISSN 0024-9297. S2CID 105834506.
Jung, Hyuk-Joon; Yu, Insun; Nyamayaro, Kudzanai; Mehrkhodavandi, Parisa (5 June 2020). "Indium-Catalyzed Block Copolymerization of Lactide and Methyl Methacrylate by Sequential Addition". ACS Catalysis. 10 (11): 6488–6496. doi:10.1021/acscatal.0c01365. ISSN 2155-5435. S2CID 219762406.
Pham, M.C; Hubert, S; Piro, B; Maurel, F; Le Dao, H; Takenouti, H (February 2004). "Investigations of the redox process of conducting poly(2-methyl-5-amino-1,4-naphthoquinone) (PMANQ) film". Synthetic Metals. 140 (2–3): 183–197. doi:10.1016/S0379-6779(03)00373-4.

elsevier.com

linkinghub.elsevier.com

Pham, M.C; Hubert, S; Piro, B; Maurel, F; Le Dao, H; Takenouti, H (February 2004). "Investigations of the redox process of conducting poly(2-methyl-5-amino-1,4-naphthoquinone) (PMANQ) film". Synthetic Metals. 140 (2–3): 183–197. doi:10.1016/S0379-6779(03)00373-4.

harvard.edu

ui.adsabs.harvard.edu

Tiano, Martin (2020). "Enantioselective Michael Addition: An Experimental Introduction to Asymmetric Synthesis". Journal of Chemical Education. 97 (8): 2291–2295. Bibcode:2020JChEd..97.2291T. doi:10.1021/acs.jchemed.0c00164.
Wong, T. C.; Sultana, C. M.; Vosburg, D. A. (2010). "A Green, Enantioselective Synthesis of Warfarin for the Undergraduate Organic Laboratory". Journal of Chemical Education. 87 (2): 194. Bibcode:2010JChEd..87..194W. doi:10.1021/ed800040m.
Huang, Sijia; Sinha, Jasmine; Podgórski, Maciej; Zhang, Xinpeng; Claudino, Mauro; Bowman, Christopher N. (14 August 2018). "Mechanistic Modeling of the Thiol–Michael Addition Polymerization Kinetics: Structural Effects of the Thiol and Vinyl Monomers". Macromolecules. 51 (15): 5979–5988. Bibcode:2018MaMol..51.5979H. doi:10.1021/acs.macromol.8b01264. ISSN 0024-9297. S2CID 105834506.

hathitrust.org

babel.hathitrust.org

Conrad, M.; Guthzeit, M. (1884). "Ueber die Einwirkung von α-β-Dibrompropionsäure auf Malonsäureester" [On the reaction of 2,3-dibrompropionic acid with [diethyl] malonic acid ester]. Berichte der Deutschen Chemischen Gesellschaft. 17 (1): 1185–1188. doi:10.1002/cber.188401701314.
Claisen, L. (1887). "Bemerkung über die Addition von Aethylmalonat an Körper mit doppelter Kohlenstoffbindung" [Observation on the addition of [di]ethyl malonate to substances with a double carbon bond]. Journal für Praktische Chemie. 2nd series. 35 (1): 413–415. doi:10.1002/prac.18870350144.
Komnenos, T. (1883). "Ueber die Einwirkung von Fettaldehyden auf Malonsäure und Aethylmalonat" [On the reaction of aliphatic aldehydes with malonic acid and [di]ethylmalonate]. Justus Liebig's Annalen der Chemie. 218 (2): 145–167. doi:10.1002/jlac.18832180204.

nih.gov

pubmed.ncbi.nlm.nih.gov

Pansare, S. V.; Pandya, K. (2006). "Simple Diamine- and Triamine-Protonic Acid Catalysts for the Enantioselective Michael Addition of Cyclic Ketones to Nitroalkenes". Journal of the American Chemical Society. 128 (30): 9624–9625. doi:10.1021/ja062701n. PMID 16866504.
Halland, N.; Hansen, T.; Jørgensen, K. (2003). "Organocatalytic asymmetric Michael reaction of cyclic 1,3-dicarbonyl compounds and α,β-unsaturated ketones--a highly atom-economic catalytic one-step formation of optically active warfarin anticoagulant". Angewandte Chemie. 42 (40): 4955–4957. doi:10.1002/anie.200352136. PMID 14579449.
Kim, H.; Yen, C.; Preston, P.; Chin, J. (2006). "Substrate-directed stereoselectivity in vicinal diamine-catalyzed synthesis of warfarin". Organic Letters. 8 (23): 5239–5242. doi:10.1021/ol062000v. PMID 17078687.
Xie, J.; Yue, L.; Chen, W.; Du, W.; Zhu, J.; Deng, J.; Chen, Y. (2007). "Highly Enantioselective Michael Addition of Cyclic 1,3-Dicarbonyl Compounds to α,β-Unsaturated Ketones". Organic Letters. 9 (3): 413–415. doi:10.1021/ol062718a. PMID 17249775.
Lippert, A. R.; Kaeobamrung, J.; Bode, J. W. (2006). "Synthesis of Oligosubstituted Bullvalones: Shapeshifting Molecules Under Basic Conditions". Journal of the American Chemical Society. 128 (46): 14738–14739. doi:10.1021/ja063900+. PMID 17105247.
den Hartog, Tim; Harutyunyan, Syuzanna R.; Font, Daniel; Minnaard, Adriaan J.; Feringa, Ben L. (January 2008). "Catalytic Enantioselective 1,6-Conjugate Addition of Grignard Reagents to Linear Dienoates". Angewandte Chemie International Edition. 47 (2): 398–401. doi:10.1002/anie.200703702. PMID 18041800.
Boike, Lydia; Henning, Nathaniel J.; Nomura, Daniel K. (25 August 2022). "Advances in covalent drug discovery". Nature Reviews Drug Discovery. 21 (12): 881–898. doi:10.1038/s41573-022-00542-z. ISSN 1474-1776. PMC 9403961. PMID 36008483.

ncbi.nlm.nih.gov

Boike, Lydia; Henning, Nathaniel J.; Nomura, Daniel K. (25 August 2022). "Advances in covalent drug discovery". Nature Reviews Drug Discovery. 21 (12): 881–898. doi:10.1038/s41573-022-00542-z. ISSN 1474-1776. PMC 9403961. PMID 36008483.

orgsyn.org

Clarke, H. T.; Murray, T. F. (1941). "1,1,2,3-Propanetetracarboxylic acid, tetraethyl ester". Organic Syntheses; Collected Volumes, vol. 1, p. 272.
Shriner, R. L.; Todd, H. R. (1943). "1,3-Cyclohexanedione, 5,5-dimethyl-". Organic Syntheses; Collected Volumes, vol. 2, p. 200.
James Cason (1963). "β-Methylglutaric anhydride". Organic Syntheses; Collected Volumes, vol. 4, p. 630.
Moffett, R. B. (1963). "Methyl γ-Methyl-γ-nitrovalerate". Organic Syntheses; Collected Volumes, vol. 4, p. 652.
Horning, E. C.; Finelli, A. F. (1963). "α-Phenyl-α-carbethoxyglutaronitrile". Organic Syntheses; Collected Volumes, vol. 4, p. 776.
McMurry, J. E.; Melton, J. (1988). "Conversion of Nitro to Carbonyl by Ozonolysis of Nitronates: 2,5-Heptanedione". Organic Syntheses; Collected Volumes, vol. 6, p. 648.

pharmaxchange.info

Michael Addition | PharmaXChange.info

sciencedirect.com

Mather, Brian D.; Viswanathan, Kalpana; Miller, Kevin M.; Long, Timothy E. (1 May 2006). "Michael addition reactions in macromolecular design for emerging technologies". Progress in Polymer Science. 31 (5): 487–531. doi:10.1016/j.progpolymsci.2006.03.001. ISSN 0079-6700.
Guin, Soumitra; Saha, Hemonta K.; Patel, Ashvani K.; Gudimella, Santosh K.; Biswas, Subhankar; Samanta, Sampak (17 July 2020). "1,6-Aza-Michael addition of para-quinone methides with N-heterocycles catalyzed by Zn(OTf)2: A regioselective approach to N-diarylmethyl-substituted heterocycles". Tetrahedron. 76 (28): 131338. doi:10.1016/j.tet.2020.131338. ISSN 0040-4020. S2CID 225589003.
Perlmutter, P., ed. (1 January 1992), "Chapter One – Introduction", Tetrahedron Organic Chemistry Series, Conjugate Addition Reactions in Organic Synthesis, vol. 9, Elsevier, pp. 1–61, doi:10.1016/b978-0-08-037067-5.50007-2, retrieved 7 October 2022

semanticscholar.org

api.semanticscholar.org

Guin, Soumitra; Saha, Hemonta K.; Patel, Ashvani K.; Gudimella, Santosh K.; Biswas, Subhankar; Samanta, Sampak (17 July 2020). "1,6-Aza-Michael addition of para-quinone methides with N-heterocycles catalyzed by Zn(OTf)2: A regioselective approach to N-diarylmethyl-substituted heterocycles". Tetrahedron. 76 (28): 131338. doi:10.1016/j.tet.2020.131338. ISSN 0040-4020. S2CID 225589003.
Hayashi, Yujiro; Okamura, Daichi; Umemiya, Shigenobu; Uchimaru, Tadafumi (July 2012). "Organocatalytic 1,4-Addition Reaction of α,β-γ,δ-Diunsaturated Aldehydes versus 1,6-Addition Reaction". ChemCatChem. 4 (7): 959–962. doi:10.1002/cctc.201200161. S2CID 98643888.
Huang, Sijia; Sinha, Jasmine; Podgórski, Maciej; Zhang, Xinpeng; Claudino, Mauro; Bowman, Christopher N. (14 August 2018). "Mechanistic Modeling of the Thiol–Michael Addition Polymerization Kinetics: Structural Effects of the Thiol and Vinyl Monomers". Macromolecules. 51 (15): 5979–5988. Bibcode:2018MaMol..51.5979H. doi:10.1021/acs.macromol.8b01264. ISSN 0024-9297. S2CID 105834506.
Jung, Hyuk-Joon; Yu, Insun; Nyamayaro, Kudzanai; Mehrkhodavandi, Parisa (5 June 2020). "Indium-Catalyzed Block Copolymerization of Lactide and Methyl Methacrylate by Sequential Addition". ACS Catalysis. 10 (11): 6488–6496. doi:10.1021/acscatal.0c01365. ISSN 2155-5435. S2CID 219762406.

ucalgary.ca

chem.ucalgary.ca

Hunt, I. "Chapter 18: Enols and Enolates – The Michael Addition reaction". University of Calgary.

wiley.com

onlinelibrary.wiley.com

Hayashi, Yujiro; Okamura, Daichi; Umemiya, Shigenobu; Uchimaru, Tadafumi (July 2012). "Organocatalytic 1,4-Addition Reaction of α,β-γ,δ-Diunsaturated Aldehydes versus 1,6-Addition Reaction". ChemCatChem. 4 (7): 959–962. doi:10.1002/cctc.201200161. S2CID 98643888.
den Hartog, Tim; Harutyunyan, Syuzanna R.; Font, Daniel; Minnaard, Adriaan J.; Feringa, Ben L. (January 2008). "Catalytic Enantioselective 1,6-Conjugate Addition of Grignard Reagents to Linear Dienoates". Angewandte Chemie International Edition. 47 (2): 398–401. doi:10.1002/anie.200703702. PMID 18041800.

worldcat.org

search.worldcat.org

Mather, Brian D.; Viswanathan, Kalpana; Miller, Kevin M.; Long, Timothy E. (1 May 2006). "Michael addition reactions in macromolecular design for emerging technologies". Progress in Polymer Science. 31 (5): 487–531. doi:10.1016/j.progpolymsci.2006.03.001. ISSN 0079-6700.
Brown, William Henry (2018). Organic chemistry. Brent L. Iverson, Eric V. Anslyn, Christopher S. Foote (Eighth ed.). Boston, Mass. ISBN 978-1-337-51640-2. OCLC 1200494733.{{cite book}}: CS1 maint: location missing publisher (link)
Guin, Soumitra; Saha, Hemonta K.; Patel, Ashvani K.; Gudimella, Santosh K.; Biswas, Subhankar; Samanta, Sampak (17 July 2020). "1,6-Aza-Michael addition of para-quinone methides with N-heterocycles catalyzed by Zn(OTf)2: A regioselective approach to N-diarylmethyl-substituted heterocycles". Tetrahedron. 76 (28): 131338. doi:10.1016/j.tet.2020.131338. ISSN 0040-4020. S2CID 225589003.
Boike, Lydia; Henning, Nathaniel J.; Nomura, Daniel K. (25 August 2022). "Advances in covalent drug discovery". Nature Reviews Drug Discovery. 21 (12): 881–898. doi:10.1038/s41573-022-00542-z. ISSN 1474-1776. PMC 9403961. PMID 36008483.
Huang, Sijia; Sinha, Jasmine; Podgórski, Maciej; Zhang, Xinpeng; Claudino, Mauro; Bowman, Christopher N. (14 August 2018). "Mechanistic Modeling of the Thiol–Michael Addition Polymerization Kinetics: Structural Effects of the Thiol and Vinyl Monomers". Macromolecules. 51 (15): 5979–5988. Bibcode:2018MaMol..51.5979H. doi:10.1021/acs.macromol.8b01264. ISSN 0024-9297. S2CID 105834506.
Jung, Hyuk-Joon; Yu, Insun; Nyamayaro, Kudzanai; Mehrkhodavandi, Parisa (5 June 2020). "Indium-Catalyzed Block Copolymerization of Lactide and Methyl Methacrylate by Sequential Addition". ACS Catalysis. 10 (11): 6488–6496. doi:10.1021/acscatal.0c01365. ISSN 2155-5435. S2CID 219762406.

worldcat.org

Brown, William Henry (2018). Organic chemistry. Brent L. Iverson, Eric V. Anslyn, Christopher S. Foote (Eighth ed.). Boston, Mass. ISBN 978-1-337-51640-2. OCLC 1200494733.{{cite book}}: CS1 maint: location missing publisher (link)