Catalytic, Enantioselective [4 + 2]-Cycloadditions of Ketene Enolates and o-Quinones: Efficient Entry to Chiral, α-Oxygenated Carboxylic Acid Derivatives-Reference-Cited by-同舟云学术

Catalytic, Enantioselective [4 + 2]-Cycloadditions of Ketene Enolates and o-Quinones: Efficient Entry to Chiral, α-Oxygenated Carboxylic Acid Derivatives

Published:2006-01-21 Issue:6 Volume:128 Page:1810-1811
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Bekele Tefsit¹,Shah Meha H.¹,Wolfer Jamison¹,Abraham Ciby J.¹,Weatherwax Anthony¹,Lectka Thomas¹

Affiliation:

1. Department of Chemistry, New Chemistry Building, Johns Hopkins University, 3400 North Charles Street, Baltimore, Maryland, 21218

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja058077g

Reference8 articles.

1. Asymmetric synthesis of (S)- and (R)-malic acid from ketene and chloral

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