Syntheses of 12H-benzo[a]xanthen-12-ones and benzo[a]acridin-12(7H)-ones through Au(i)-catalyzed Michael addition/6-endo-trig cyclization/aromatization cascade annulation-Reference-Cited by-同舟云学术

Syntheses of 12H-benzo[a]xanthen-12-ones and benzo[a]acridin-12(7H)-ones through Au(i)-catalyzed Michael addition/6-endo-trig cyclization/aromatization cascade annulation

Published:2018 Issue:40 Volume:16 Page:7361-7374
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Xiong Zhiling¹²³⁴⁵,Zhang Xinhang¹²³⁴⁵,Li Yangming¹²³⁴⁵,Peng Xiaoshi¹²³⁴⁵,Fu Jiayue¹²³⁴⁵,Guo Jiajia¹²³⁴⁵,Xie Fukai¹²³⁴⁵,Jiang Chongguo¹²³⁴⁵,Lin Bin¹²³⁴⁵,Liu Yongxiang¹²³⁴⁵^ORCID,Cheng Maosheng¹²³⁴⁵

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

A gold(i)-catalyzed cascade strategy to synthesize both 12H-benzo[a]xanthen-12-ones and benzo[a]acridin-12(7H)-ones was developed.

Funder

National Natural Science Foundation of China

Foundation of Liaoning Province Education Administration

Publisher