Dieckmann Condensation of Ugi N-Acylamino Amide Product: Facile Access to Functionalized 2,2-Disubstituted Indolin-3-ones-Reference-Cited by-同舟云学术

Dieckmann Condensation of Ugi N-Acylamino Amide Product: Facile Access to Functionalized 2,2-Disubstituted Indolin-3-ones

Published:2021-12-17 Issue:1 Volume:87 Page:823-834
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Li Yong¹,Xu Jia¹,He Liu-Jun¹,Luo Ya-Fei¹,Meng Jiang-Ping¹,Tang Dian-Yong¹,Li Hong-yu²^ORCID,Chen Zhong-Zhu¹,Xu Zhi-Gang¹^ORCID

Affiliation:

1. College of Pharmacy, National & Local Joint Engineering Research Center of Targeted and Innovative Therapeutics, IATTI, Chongqing University of Arts and Sciences, 319 Honghe Avenue, Yongchuan, Chongqing 402160, China

2. Department of Pharmaceutical Sciences, College of Pharmacy, University of Arkansas for Medical Sciences, Little Rock, Arkansas 72205, United States

Funder

Chongqing Research Program of Basic Research and Frontier Technology

Chongqing Municipal Education Commission

Chongqing University of Arts and Sciences

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.1c02501

Reference77 articles.

1. Asymmetric, stereocontrolled total synthesis of (-)-brevianamide B