Molecular design principles towards exo-exclusive Diels–Alder reactions-Reference-Cited by-同舟云学术

Molecular design principles towards exo-exclusive Diels–Alder reactions

Published:2019 Issue:13 Volume:9 Page:7246-7250
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Huang Ci-Jhang¹²³⁴,Li Elise Y.¹²³⁴^ORCID

Affiliation:

1. Department of Chemistry

2. National Taiwan Normal University

3. Taipei

4. Taiwan

Abstract

Exo-exclusive stereoselectivity for simple, terminal-substituted dienes and dienophiles may be achieved under thermal conditions through a delicate control of substituent identities.

Funder

Ministry of Science and Technology, Taiwan

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/RA/C8RA10438G

Reference47 articles.

1. Synthesen in der hydroaromatischen Reihe

2. Untersuchungen über den Verlauf der Diensynthese

3. Orbital Symmetries and endo-exo Relationships in Concerted Cycloaddition Reactions

4. The existence of secondary orbital interactions

5. Do Secondary Orbital Interactions Really Exist?

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