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Highly enantioselective organocatalytic direct aldol reaction in an aqueous medium.
Org Lett. 2007 Jun 21; 9(13):2593-5.OL

Abstract

We have demonstrated that small organic molecules 1 and 2 catalyzed the direct aldol reaction of both acyclic and cyclic ketones with different aldehydes in an excess of water/brine. Excellent enantioselectivities up to >99% and diastereoselectivities up to 99% with very good yields were obtained by using much lower catalyst loadings (0.5 mol %).

Authors+Show Affiliations

Deparment of Chemistry, Indian Institute of Technology Kanpur, India 208 016.No affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

17518481

Citation

Maya, Vishnu, et al. "Highly Enantioselective Organocatalytic Direct Aldol Reaction in an Aqueous Medium." Organic Letters, vol. 9, no. 13, 2007, pp. 2593-5.
Maya V, Raj M, Singh VK. Highly enantioselective organocatalytic direct aldol reaction in an aqueous medium. Org Lett. 2007;9(13):2593-5.
Maya, V., Raj, M., & Singh, V. K. (2007). Highly enantioselective organocatalytic direct aldol reaction in an aqueous medium. Organic Letters, 9(13), 2593-5.
Maya V, Raj M, Singh VK. Highly Enantioselective Organocatalytic Direct Aldol Reaction in an Aqueous Medium. Org Lett. 2007 Jun 21;9(13):2593-5. PubMed PMID: 17518481.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Highly enantioselective organocatalytic direct aldol reaction in an aqueous medium. AU - Maya,Vishnu, AU - Raj,Monika, AU - Singh,Vinod K, Y1 - 2007/05/23/ PY - 2007/5/24/pubmed PY - 2007/5/24/medline PY - 2007/5/24/entrez SP - 2593 EP - 5 JF - Organic letters JO - Org Lett VL - 9 IS - 13 N2 - We have demonstrated that small organic molecules 1 and 2 catalyzed the direct aldol reaction of both acyclic and cyclic ketones with different aldehydes in an excess of water/brine. Excellent enantioselectivities up to >99% and diastereoselectivities up to 99% with very good yields were obtained by using much lower catalyst loadings (0.5 mol %). SN - 1523-7060 UR - https://www.unboundmedicine.com/medline/citation/17518481/Highly_enantioselective_organocatalytic_direct_aldol_reaction_in_an_aqueous_medium_ L2 - https://doi.org/10.1021/ol071013l DB - PRIME DP - Unbound Medicine ER -
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