Diversity-oriented synthesis of chromenopyrrolidines from azomethine ylides and 2-hydroxybenzylidene indandiones via base-controlled regiodivergent (3+2) cycloaddition-Reference-Cited by-同舟云学术

Diversity-oriented synthesis of chromenopyrrolidines from azomethine ylides and 2-hydroxybenzylidene indandiones via base-controlled regiodivergent (3+2) cycloaddition

Published:2018 Issue:71 Volume:54 Page:9921-9924
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Yu Jhen-Kuei¹²³⁴,Chien Han-Wei¹²³⁴,Lin Yi-Jung¹²³⁴,Karanam Praneeth¹²³⁴,Chen Yu-Heng¹²³⁴,Lin Wenwei¹²³⁴^ORCID

Affiliation:

1. Department of Chemistry

2. National Taiwan Normal University

3. Taipei 11677

4. Republic of China

Abstract

An organobase-controlled, regiodivergent (3+2) cycloaddition resulting in two different cascade reactions is demonstrated from azomethine ylides and 2-hydroxybenzylidineindandiones to achieve diverse chromanopyrrolidines.

Funder

Ministry of Science and Technology of the People's Republic of China

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/2018/CC/C8CC05693E

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