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Enantioselective organocatalytic Michael addition reactions between N-heterocycles and nitroolefins.
Org Lett. 2006 Mar 30; 8(7):1391-4.OL

Abstract

[reaction: see text] A method for Michael addition of N-heterocycles to nitroolefins has been developed. The process is promoted by a cinchona alkaloid derivative to give Michael adducts in moderate to high enantioselectivities.

Authors+Show Affiliations

Wang J
Department of Chemistry, University of New Mexico, Albuquerque, New Mexico 87131-0001, USA.
Li H
No affiliation info available
Zu L
No affiliation info available
Wang W
No affiliation info available

MeSH

AlkenesCatalysisCinchona AlkaloidsMolecular StructureNitro CompoundsStereoisomerism

Pub Type(s)

Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

16562899

Citation

Wang, Jian, et al. "Enantioselective Organocatalytic Michael Addition Reactions Between N-heterocycles and Nitroolefins." Organic Letters, vol. 8, no. 7, 2006, pp. 1391-4.
Wang J, Li H, Zu L, et al. Enantioselective organocatalytic Michael addition reactions between N-heterocycles and nitroolefins. Org Lett. 2006;8(7):1391-4.
Wang, J., Li, H., Zu, L., & Wang, W. (2006). Enantioselective organocatalytic Michael addition reactions between N-heterocycles and nitroolefins. Organic Letters, 8(7), 1391-4.
Wang J, et al. Enantioselective Organocatalytic Michael Addition Reactions Between N-heterocycles and Nitroolefins. Org Lett. 2006 Mar 30;8(7):1391-4. PubMed PMID: 16562899.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Enantioselective organocatalytic Michael addition reactions between N-heterocycles and nitroolefins. AU - Wang,Jian, AU - Li,Hao, AU - Zu,Liansuo, AU - Wang,Wei, PY - 2006/3/28/pubmed PY - 2006/12/22/medline PY - 2006/3/28/entrez SP - 1391 EP - 4 JF - Organic letters JO - Org Lett VL - 8 IS - 7 N2 - [reaction: see text] A method for Michael addition of N-heterocycles to nitroolefins has been developed. The process is promoted by a cinchona alkaloid derivative to give Michael adducts in moderate to high enantioselectivities. SN - 1523-7060 UR - https://www.unboundmedicine.com/medline/citation/16562899/Enantioselective_organocatalytic_Michael_addition_reactions_between_N_heterocycles_and_nitroolefins_ DB - PRIME DP - Unbound Medicine ER -