A DFT Study of N-Heterocyclic Carbene Catalyzed [4+2] Annulation between Saturated Carboxylate withortho-Quinone Methide: Possible Mechanisms and Origin of Enantioselectivity-Reference-Cited by-同舟云学术

A DFT Study of N-Heterocyclic Carbene Catalyzed [4+2] Annulation between Saturated Carboxylate withortho-Quinone Methide: Possible Mechanisms and Origin of Enantioselectivity

Published:2017-09-29 Issue:28 Volume:2 Page:8856-8864
ISSN:2365-6549
Container-title:ChemistrySelect
language:en
Short-container-title:ChemistrySelect

Author:

Wang Wei¹^ORCID,Wei Donghui¹

Affiliation:

1. The College of Chemistry and Molecular Engineering; Center of Computational Chemistry; Zhengzhou University; Zhengzhou, Henan Province 450001 P. R. China

Funder

National Natural Science Foundation of China

China Postdoctoral Science Foundation

Outstanding Young Talent Research Fund of Zhengzhou University

Publisher

Wiley

Subject

General Chemistry

Reference72 articles.

1. Coumarin heterocyclic derivatives: chemical synthesis and biological activity

2. Asymmetric Synthesis of Dihydrocoumarins Containing Contiguous Quaternary and Tertiary Stereogenic Centers Catalyzed by aCinchona-Alkaloid-Based Bifunctional Thiourea Derivative

3. Enantioselective Synthesis of 4-Substituted Dihydrocoumarins through a Zinc Bis(hydroxyamide)-Catalyzed Conjugate Addition of Terminal Alkynes

4. PdI2-Catalyzed Regioselective Cyclocarbonylation of 2-Allyl Phenols to Dihydrocoumarins

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