Unusual Sterically Controlled Regioselective Lithiation of 3-Bromo-5-(4,4‘-dimethyl)oxazolinylpyridine. Straightforward Access to Highly Substituted Nicotinic Acid Derivatives-Reference-Cited by-同舟云学术

Unusual Sterically Controlled Regioselective Lithiation of 3-Bromo-5-(4,4‘-dimethyl)oxazolinylpyridine. Straightforward Access to Highly Substituted Nicotinic Acid Derivatives

Published:2006-12-01 Issue:26 Volume:8 Page:6071-6074
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Robert Nicolas¹,Bonneau Anne-Laure¹,Hoarau Christophe¹,Marsais Francis¹

Affiliation:

1. Laboratoire de Chimie Organique Fine et Hétérocyclique, UMR 6014, INSA et Université de Rouen, IRCOF-INSA Rouen BP08, 76131 Mont Saint Aignan Cedex, France

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol062556i

Reference27 articles.

1. Reviews: (a) Offermanns, H.; Kleemann, A.; Tanner, H.; Beschke, H.; Friedrich, H. InKirk-Othmer Encyclopedia of Chemical Technology, 3rd ed.; Grayson, M., Eckroth, D., Eds; Wiley: New York, 1983; p 59. (b) Sharmann, I. M.Nutr. Food Sci.1982,77, 17−19.

2. Stereoselective synthesis of nicotinamide β-riboside and nucleoside analogs

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