Chemoselective acid-catalyzed [4 + 2]-cycloaddition reactions of ortho-quinone methides and styrenes/stilbenes/cinnamates-Reference-Cited by-同舟云学术

Chemoselective acid-catalyzed [4 + 2]-cycloaddition reactions of ortho-quinone methides and styrenes/stilbenes/cinnamates

Published:2020 Issue:43 Volume:18 Page:8854-8866
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Akkarasereenon Kornkamon¹²³⁴⁵,Tangdenpaisal Kassrin⁶⁷⁴⁵,Ruchirawat Somsak¹²³⁴⁵,Ploypradith Poonsakdi¹²³⁴⁵^ORCID

Affiliation:

1. Program in Chemical Sciences

2. Chulabhorn Graduate Institute

3. Chulabhorn Royal Academy

4. Bangkok

5. Thailand

6. Laboratory of Medicinal Chemistry

7. Chulabhorn Research Institute

Abstract

Chemoselective [4 + 2]-cycloaddition reactions between o-QMs and different olefins—styrenes, stilbenes, and cinnamates—yielded distinct cycloadducts in moderate to good yields.

Funder

Thailand Research Fund

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/OB/D0OB01312A

Reference58 articles.

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2. Stereoselective Reactions of ortho-Quinone Methide and ortho-Quinone Methide Imines and Their Utility in Natural Product Synthesis

3. Mannich base-connected syntheses mediated by ortho-quinone methides

4. ortho-Quinone methides as key intermediates in cascade heterocyclizations

5. The Emergence of Quinone Methides in Asymmetric Organocatalysis

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