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Alpha-aminophosphonates as novel organocatalysts for asymmetric Michael addition of carbonyl compounds to nitroolefins.
Chirality. 2008 Jul; 20(7):833-8.C

Abstract

A cyclic alpha-aminophosphonate was found to be a novel organocatalyst for Michael type addition reactions of carbonyl compounds to nitroolefins to afford the corresponding adducts in high enantio- and diastereoselectivities.

Authors+Show Affiliations

Department of Chemistry and Key Laboratory for Chemical Biology of Fujian Province, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, People's Republic of China.No affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

18381740

Citation

Tao, Qin, et al. "Alpha-aminophosphonates as Novel Organocatalysts for Asymmetric Michael Addition of Carbonyl Compounds to Nitroolefins." Chirality, vol. 20, no. 7, 2008, pp. 833-8.
Tao Q, Tang G, Lin K, et al. Alpha-aminophosphonates as novel organocatalysts for asymmetric Michael addition of carbonyl compounds to nitroolefins. Chirality. 2008;20(7):833-8.
Tao, Q., Tang, G., Lin, K., & Zhao, Y. F. (2008). Alpha-aminophosphonates as novel organocatalysts for asymmetric Michael addition of carbonyl compounds to nitroolefins. Chirality, 20(7), 833-8. https://doi.org/10.1002/chir.20552
Tao Q, et al. Alpha-aminophosphonates as Novel Organocatalysts for Asymmetric Michael Addition of Carbonyl Compounds to Nitroolefins. Chirality. 2008;20(7):833-8. PubMed PMID: 18381740.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Alpha-aminophosphonates as novel organocatalysts for asymmetric Michael addition of carbonyl compounds to nitroolefins. AU - Tao,Qin, AU - Tang,Guo, AU - Lin,Kan, AU - Zhao,Yu-Fen, PY - 2008/4/3/pubmed PY - 2008/6/28/medline PY - 2008/4/3/entrez SP - 833 EP - 8 JF - Chirality JO - Chirality VL - 20 IS - 7 N2 - A cyclic alpha-aminophosphonate was found to be a novel organocatalyst for Michael type addition reactions of carbonyl compounds to nitroolefins to afford the corresponding adducts in high enantio- and diastereoselectivities. SN - 1520-636X UR - https://www.unboundmedicine.com/medline/citation/18381740/Alpha_aminophosphonates_as_novel_organocatalysts_for_asymmetric_Michael_addition_of_carbonyl_compounds_to_nitroolefins_ DB - PRIME DP - Unbound Medicine ER -