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Highly enantioselective water-compatible organocatalyst for Michael reaction of ketones to nitroolefins.
Org Lett. 2007 Mar 15; 9(6):1117-9.OL

Abstract

A chiral diamine was found to catalyze enantioselective addition of ketones to nitroolefins in aqueous/saline/organic media. The products were obtained with excellent diastereoselectivities (syn/anti = 99:1) and enantioselectivities up to 99%. The reaction could be facilitated using a mild acid. [reaction: see text]

Authors+Show Affiliations

Department of Chemistry, Indian Institute of Technology, Kanpur, India-208 016.No affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

17316013

Citation

Vishnumaya, , and Vinod K. Singh. "Highly Enantioselective Water-compatible Organocatalyst for Michael Reaction of Ketones to Nitroolefins." Organic Letters, vol. 9, no. 6, 2007, pp. 1117-9.
Vishnumaya , Singh VK. Highly enantioselective water-compatible organocatalyst for Michael reaction of ketones to nitroolefins. Org Lett. 2007;9(6):1117-9.
Vishnumaya, ., & Singh, V. K. (2007). Highly enantioselective water-compatible organocatalyst for Michael reaction of ketones to nitroolefins. Organic Letters, 9(6), 1117-9.
Vishnumaya , Singh VK. Highly Enantioselective Water-compatible Organocatalyst for Michael Reaction of Ketones to Nitroolefins. Org Lett. 2007 Mar 15;9(6):1117-9. PubMed PMID: 17316013.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Highly enantioselective water-compatible organocatalyst for Michael reaction of ketones to nitroolefins. AU - Vishnumaya,, AU - Singh,Vinod K, Y1 - 2007/02/23/ PY - 2007/2/24/pubmed PY - 2007/2/24/medline PY - 2007/2/24/entrez SP - 1117 EP - 9 JF - Organic letters JO - Org Lett VL - 9 IS - 6 N2 - A chiral diamine was found to catalyze enantioselective addition of ketones to nitroolefins in aqueous/saline/organic media. The products were obtained with excellent diastereoselectivities (syn/anti = 99:1) and enantioselectivities up to 99%. The reaction could be facilitated using a mild acid. [reaction: see text] SN - 1523-7060 UR - https://www.unboundmedicine.com/medline/citation/17316013/Highly_enantioselective_water_compatible_organocatalyst_for_Michael_reaction_of_ketones_to_nitroolefins_ L2 - https://doi.org/10.1021/ol070082x DB - PRIME DP - Unbound Medicine ER -
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