Indium-Mediated Asymmetric Barbier-Type Allylation of Aldimines in Alcoholic Solvents: Synthesis of Optically Active Homoallylic Amines-Reference-Cited by-同舟云学术

Indium-Mediated Asymmetric Barbier-Type Allylation of Aldimines in Alcoholic Solvents: Synthesis of Optically Active Homoallylic Amines

Published:2005-04-01 Issue:9 Volume:70 Page:3464-3471
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Vilaivan Tirayut¹,Winotapan Chutima¹,Banphavichit Vorawit¹,Shinada Tetsuro¹,Ohfune Yasufumi¹

Affiliation:

1. Organic Synthesis Research Unit, Department of Chemistry, Faculty of Science, Chulalongkorn University, Phayathai Road, Patumwan, Bangkok 10330, Thailand, and Department of Material Sciences, Graduate School of Science, Osaka City University, Sugimoto, Sumiyoshi, Osaka 558-8585, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0477244

Reference40 articles.

1. Carbohydrates as chiral templates: diastereoselective synthesis of N-glycosyl-N-homoallylamines and .beta.-amino acids from imines

2. An efficient route to 1,3-amino hydroxyl system via electrophilic lactonization of 2-amino-4-pentenoic acid derivatives. Stereoselective synthesis of (−)-bulgecinine

3. Allylsilanes derived from aminoacids in the synthesis of piperidine and pyrrolidins derivatives

4. Stereoselective Synthesis of 2-Substituted Pyrrolidines

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