Synthesis of Central Chirality-Containing Triarylmethanols and Triarylmethyl Radicals with Extraordinarily Stable Configurations-Reference-Cited by-同舟云学术

Synthesis of Central Chirality-Containing Triarylmethanols and Triarylmethyl Radicals with Extraordinarily Stable Configurations

Published:2019-08-27 Issue:18 Volume:84 Page:11774-11782
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Li Yingchun¹,Zhai Weixiang¹,Liao Yongfang¹,Nie Jiangping¹,Han Guifang¹,Song Yuguang¹,Li Shaoyong¹,Hou Jingli¹^ORCID,Liu Yangping¹^ORCID

Affiliation:

1. Tianjin Key Laboratory on Technologies Enabling Development of Clinical Therapeutics and Diagnostics, School of Pharmacy, Tianjin Medical University, Tianjin 300070, P. R. China

Funder

National Natural Science Foundation of China

Tianjin Medical University

Science and Technology Projects of Tianjin

Tianjin Key Laboratory on Technologies Enabling Development of Clinical Therapeutics and Diagnostics,Tianjin Medical University

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.9b01675

Reference40 articles.

1. Configurationally Stable Molecular Propellers: First Resolution of Residual Enantiomers

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3. Triphenylacetic Acid Amides: Molecular Propellers with Induced Chirality

4. Stereochemical consequences of correlated rotation in molecular propellers

5. Understanding Internal Chirality Induction of Triarylsilyl Ethers Formed from Enantiopure Alcohols

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