Gold(i)-catalyzed tandem cyclization of cyclopropylidene-tethered propargylic alcohols: an approach to functionalized naphtho[2,3-c]pyrans-Reference-Cited by-同舟云学术

Gold(i)-catalyzed tandem cyclization of cyclopropylidene-tethered propargylic alcohols: an approach to functionalized naphtho[2,3-c]pyrans

Published:2020 Issue:64 Volume:56 Page:9154-9157
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Li Jian¹²³⁴⁵^ORCID,Yang Fang¹²³⁴⁵,Hu Weiwei¹²³⁴⁵,Ren Bo¹²³⁴⁵,Chen Zi-Sheng¹²³⁴⁵^ORCID,Ji Kegong¹²³⁴⁵^ORCID

Affiliation:

1. Shaanxi Key Laboratory of Natural Products & Chemical Biology

2. College of Chemistry and Pharmacy

3. Northwest A&F University

4. Yangling 712100

5. P. R. China

Abstract

An unprecedented gold(i)-catalyzed cyclization of cyclopropylidene-tethered ynols via a 6-endo-dig enyne cyclization followed by a ring-opening of cyclopropane and nucleophilic closure reaction to construct naphtho[2,3-c]pyrans was developed.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Shaanxi Province

Northwest A and F University

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2020/CC/D0CC03285A

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5. Naphthopyran-Based Silica Nanoparticles as New High-Performance Photoresponsive Materials

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