Dipole‐bound states and substituent effects of Breslow intermediates in the enolate form-Reference-Cited by-同舟云学术

Dipole‐bound states and substituent effects of Breslow intermediates in the enolate form

Published:2021-08-31 Issue:11 Volume:68 Page:2060-2070
ISSN:0009-4536
Container-title:Journal of the Chinese Chemical Society
language:en
Short-container-title:J Chin Chem Soc

Author:

Hsieh Ming‐Hsiu¹,Huang Gou‐Tao²,Yu Jen‐Shiang K.³⁴

Affiliation:

1. Institute of Bioinformatics and Systems Biology National Yang Ming Chiao Tung University Hsinchu Taiwan

2. Department of Biological Science and Technology National Yang Ming Chiao Tung University Hsinchu Taiwan

3. Institute of Bioinformatics and Systems Biology, Department of Biological Science and Technology, and Institute of Molecular Medicine and Bioengineering National Yang Ming Chiao Tung University Hsinchu Taiwan

4. Center for Intelligent Drug Systems and Smart Bio‐Devices National Yang Ming Chiao Tung University Hsinchu Taiwan

Funder

Ministry of Education

Ministry of Science and Technology

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jccs.202100310

Reference57 articles.

1. On the Mechanism of Thiamine Action. IV.1 Evidence from Studies on Model Systems

2. Organocatalytic umpolung: N-heterocyclic carbenes and beyond

3. Organocatalytic Reactions Enabled by N-Heterocyclic Carbenes

4. Tale of the Breslow intermediate, a central player in N-heterocyclic carbene organocatalysis: then and now

5. Characterization of the Key Intermediates of Carbene-Catalyzed Umpolung by NMR Spectroscopy and X-Ray Diffraction: Breslow Intermediates, Homoenolates, and Azolium Enolates

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