Theoretical Studies of the Asymmetric Binary‐Acid‐Catalyzed tert ‐Aminocyclization Reaction: Origins of the CH Activation and Stereoselectivity-Reference-Cited by-同舟云学术

Theoretical Studies of the Asymmetric Binary‐Acid‐Catalyzed tert ‐Aminocyclization Reaction: Origins of the CH Activation and Stereoselectivity

Published:2012-09-10 Issue:11 Volume:7 Page:2569-2576
ISSN:1861-4728
Container-title:Chemistry – An Asian Journal
language:en
Short-container-title:Chemistry An Asian Journal

Author:

Zhang Long¹,Chen Liujuan¹,Lv Jian¹,Cheng Jin‐Pei¹,Luo Sanzhong¹

Affiliation:

1. Beijing National Laboratory for Molecular Sciences (BNLMS), CAS Key of Molecular Recognition and Function Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190 (China), Fax: (+86) 10‐62554449 http://luosz.iccas.ac.cn

Publisher

Wiley

Subject

General Chemistry,Biochemistry,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/asia.201200674

Reference76 articles.

2. Heterocycles by Ring Closure of Ortho-Substituted t-Anilines (The t-Amino Effect)

3. The t-Amino Effect: Heterocycles Formed by Ring Closure of ortho-Substituted t-Anilines**Dedicated to my evergreen friend and mentor, Professor Hans Suschitzky, on his 80th birthday.

5. Ring-Closure Reactions of ortho-Vinyl-tert-anilines and (Di)Aza-Heterocyclic Analogues via the tert-Amino Effect: Recent Developments

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