Rhodium-Catalyzed 1,4-Addition of Lithium 2-Furyltriolborates to Unsaturated Ketones and Esters for Enantioselective Synthesis of γ-Oxo-Carboxylic Acids By Oxidation of the Furyl Ring with Ozone-Reference-Cited by-同舟云学术

Rhodium-Catalyzed 1,4-Addition of Lithium 2-Furyltriolborates to Unsaturated Ketones and Esters for Enantioselective Synthesis of γ-Oxo-Carboxylic Acids By Oxidation of the Furyl Ring with Ozone

Published:2011-01-04 Issue:3 Volume:6 Page:932-937
ISSN:1861-4728
Container-title:Chemistry - An Asian Journal
language:en
Short-container-title:Chem. Asian J.

Author:

Yu Xiao-Qiang,Shirai Tomohiko,Yamamoto Yasunori,Miyaura Norio

Publisher

Wiley

Subject

General Chemistry,Biochemistry,Organic Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/asia.201000589/fullpdf

Reference112 articles.

1. Stereoselective synthesis of quaternary α-amino acids. Part 1: Acyclic compounds

2. A new chiral alkylation methodology for the synthesis of 2-alkyl-4-ketoacids in high optical purity using 2-triflyloxy esters

3. The Stereoselective Synthesis of 2-Alkyl .gamma.-Keto Acid and Heterocyclic Ketomethylene Peptide Isostere Core Units Using Chiral Alkylation by 2-Triflyloxy Esters

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