Highly Regio- and Stereoselective Synthesis of Z and E Enol Esters by an Amine-Catalyzed Conjugate Addition–Rearrangement Reaction of Ynals with Carboxylic Acids-Reference-Cited by-同舟云学术

Highly Regio- and Stereoselective Synthesis of Z and E Enol Esters by an Amine-Catalyzed Conjugate Addition–Rearrangement Reaction of Ynals with Carboxylic Acids

Published:2016-10-31 Issue:12 Volume:6 Page:8030-8035
ISSN:2155-5435
Container-title:ACS Catalysis
language:en
Short-container-title:ACS Catal.

Author:

Huang He¹,Zhang Xinshuai¹,Yu Chenguang¹,Li Xiangmin¹²,Zhang Yueteng¹,Wang Wei¹²

Affiliation:

1. Department of Chemistry & Chemical Biology, University of New Mexico, Albuquerque, New Mexico 87131-0001, United States

2. State Key Laboratory of Bioengineering Reactor, Shanghai Key Laboratory of New Drug Design, Shanghai Key Laboratory of Chemical Biology, and School of Pharmacy, East China University of Science & Technology, Shanghai 200237, People’s Republic of China

Funder

Division of Chemistry

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Catalysis,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acscatal.6b02206

Reference62 articles.

1. A Novel Dietary Sesquiterpene from the marine SacoglossanTridachia Crispata

2. Grenadadiene and Grenadamide, Cyclopropyl-Containing Fatty Acid Metabolites from the Marine Cyanobacterium Lyngbya majuscula