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Ionic liquid-supported (ILS) (S)-pyrrolidine sulfonamide, a recyclable organocatalyst for the highly enantioselective Michael addition to nitroolefins.
Org Lett. 2009 Feb 19; 11(4):1037-40.OL

Abstract

A new class of ionic liquid supported (ILS) (S)-pyrrolidine sulfonamide organocatalyst has been developed and shown to be a very effective catalyst for the asymmetric Michael addition reactions of ketones and aldehyde to nitroolefins with high enantio- and diastereoselectivities. This ILS organocatalyst is also easily recycled and could be reused at least five times without significant loss of its ability to affect the outcome of the asymmetric reactions.

Authors+Show Affiliations

Department of Chemistry, Texas A&M University-Commerce, Commerce, Texas 75429-3011, USA. bukuo_ni@tamu-commerce.eduNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

19178161

Citation

Ni, Bukuo, et al. "Ionic Liquid-supported (ILS) (S)-pyrrolidine Sulfonamide, a Recyclable Organocatalyst for the Highly Enantioselective Michael Addition to Nitroolefins." Organic Letters, vol. 11, no. 4, 2009, pp. 1037-40.
Ni B, Zhang Q, Dhungana K, et al. Ionic liquid-supported (ILS) (S)-pyrrolidine sulfonamide, a recyclable organocatalyst for the highly enantioselective Michael addition to nitroolefins. Org Lett. 2009;11(4):1037-40.
Ni, B., Zhang, Q., Dhungana, K., & Headley, A. D. (2009). Ionic liquid-supported (ILS) (S)-pyrrolidine sulfonamide, a recyclable organocatalyst for the highly enantioselective Michael addition to nitroolefins. Organic Letters, 11(4), 1037-40. https://doi.org/10.1021/ol900003e
Ni B, et al. Ionic Liquid-supported (ILS) (S)-pyrrolidine Sulfonamide, a Recyclable Organocatalyst for the Highly Enantioselective Michael Addition to Nitroolefins. Org Lett. 2009 Feb 19;11(4):1037-40. PubMed PMID: 19178161.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Ionic liquid-supported (ILS) (S)-pyrrolidine sulfonamide, a recyclable organocatalyst for the highly enantioselective Michael addition to nitroolefins. AU - Ni,Bukuo, AU - Zhang,Qianying, AU - Dhungana,Kritanjali, AU - Headley,Allan D, PY - 2009/1/31/entrez PY - 2009/1/31/pubmed PY - 2009/1/31/medline SP - 1037 EP - 40 JF - Organic letters JO - Org Lett VL - 11 IS - 4 N2 - A new class of ionic liquid supported (ILS) (S)-pyrrolidine sulfonamide organocatalyst has been developed and shown to be a very effective catalyst for the asymmetric Michael addition reactions of ketones and aldehyde to nitroolefins with high enantio- and diastereoselectivities. This ILS organocatalyst is also easily recycled and could be reused at least five times without significant loss of its ability to affect the outcome of the asymmetric reactions. SN - 1523-7052 UR - https://www.unboundmedicine.com/medline/citation/19178161/Ionic_liquid_supported__ILS___S__pyrrolidine_sulfonamide_a_recyclable_organocatalyst_for_the_highly_enantioselective_Michael_addition_to_nitroolefins_ DB - PRIME DP - Unbound Medicine ER -
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