A cascade Claisen rearrangement/o-quinone methide formation/electrocyclization approach to 2H-chromenes-Reference-Cited by-同舟云学术

A cascade Claisen rearrangement/o-quinone methide formation/electrocyclization approach to 2H-chromenes

Published:2017 Issue:44 Volume:53 Page:6021-6024
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Song Liyan¹²³⁴⁵^ORCID,Huang Fang¹²³⁴⁵,Guo Liwen¹²³⁴⁵,Ouyang Ming-An¹²³⁴⁵,Tong Rongbiao⁶⁷⁸⁵^ORCID

Affiliation:

1. State Key Laboratory of Ecological Pest Control for Fujian and Taiwan Crops

2. Institute of Plant Virology

3. Fujian Agriculture and Forestry University

4. Fuzhou

5. China

6. Department of Chemistry

7. The Hong Kong University of Science and Technology

8. Kowloon

Abstract

A new approach to 8-substituted 2H-chromenes is developed, featuring a novel cascade aromatic Claisen rearrangement/o-quinone methide formation/6π-electrocyclization.

Funder

Natural Science Foundation of Fujian Province

Research Grants Council, University Grants Committee, Hong Kong

National Natural Science Foundation 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/2017/CC/C7CC03037A

Reference72 articles.

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3. Catalytic Synthesis of 2H-Chromenes

4. Rhodium-Catalyzed (5+1) Annulations Between 2-Alkenylphenols and Allenes: A Practical Entry to 2,2-Disubstituted 2H-Chromenes

5. Metalloradical Approach to 2H-Chromenes

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