Benzotriazole-Mediated Stereoselective Olefination of Carboxylic Esters: Transformation of α-Amino Acid Esters into Chiral Allylamines-Reference-Cited by-同舟云学术

Benzotriazole-Mediated Stereoselective Olefination of Carboxylic Esters: Transformation of α-Amino Acid Esters into Chiral Allylamines

Published:1998-04-28 Issue:10 Volume:63 Page:3438-3444
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Katritzky Alan R.¹,Cheng Dai¹,Li Jianqing¹

Affiliation:

1. Center for Heterocyclic Compounds, Department of Chemistry, University of Florida, Gainesville, Florida 32611-7200

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo971546f

Reference45 articles.

1. Stereoselective Olefination of Carbonyl Compounds with N-Benzyl- and N-Allylbenzotriazoles by Low-Valent Titanium-Promoted Dehydroxybenzotriazolylation

2. (a) Maguire, A. R. InComprehensive Organic Functional Group Transformations; Katritzky, A. R., Meth-Cohn, O., Rees, C. W., Eds.; Pergamon Press: New York, 1995; Vol. 1, p 589.

3. (b) Gosney, I.; Lloyd, D.ibid., p 719.

4. Alkene Synthesis

5. Carbonyl-coupling reactions using low-valent titanium

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5. References;Handbook of Heterocyclic Chemistry;2010