N-Fluorobenzenesulfonimide as a highly effective Ag(i)-catalyst attenuator for tryptamine-derived ynesulfonamide cycloisomerization-Reference-Cited by-同舟云学术

N-Fluorobenzenesulfonimide as a highly effective Ag(i)-catalyst attenuator for tryptamine-derived ynesulfonamide cycloisomerization

Published:2019 Issue:8 Volume:17 Page:2247-2257
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Pang Yadong¹²³⁴⁵,Liang Guoduan¹²³⁴⁵,Xie Fukai¹²³⁴⁵,Hu Haibin¹²³⁴⁵,Du Chuan¹²³⁴⁵,Zhang Xinhang¹²³⁴⁵,Cheng Maosheng¹²³⁴⁵,Lin Bin¹²³⁴⁵,Liu Yongxiang¹²³⁴⁵^ORCID

Affiliation:

1. Key Laboratory of Structure-Based Drug Design and Discovery Shenyang Pharmaceutical University

2. Ministry of Education

3. Shenyang 110016

4. P. R. China

5. Institute of Drug Research in Medicine Capital of China

Abstract

N-Fluorobenzenesulfonimide was identified for the first time as a unique Ag(i)-catalyst attenuator in the annulation of a tryptamine-derived ynesulfonamide to an azepino[4,5-b]indole.

Funder

Foundation of Liaoning Province Education Administration

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/OB/C9OB00059C

Reference68 articles.

1. Gold(I)-Catalyzed Intramolecular Enantioselective Hydroarylation of Allenes with Indoles

2. Gold Catalysis: The Benefits of N and N,O Ligands

3. Room Temperature Hydroamination of N-Alkenyl Ureas Catalyzed by a Gold(I) N-Heterocyclic Carbene Complex