Highly Diastereo‐ and Enantioselective Aza‐Mannich Addition of Oxazolones to N‐ Boc Protected α‐Amido Sulfones Catalyzed by Bifunctional Thiourea‐modified Cinchona Alkaloid-Reference-Cited by-同舟云学术

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Highly Diastereo‐ and Enantioselective Aza‐Mannich Addition of Oxazolones to N‐ Boc Protected α‐Amido Sulfones Catalyzed by Bifunctional Thiourea‐modified Cinchona Alkaloid

Published:2021-09-15 Issue:35 Volume:6 Page:9442-9446
ISSN:2365-6549
Container-title:ChemistrySelect
language:en
Short-container-title:ChemistrySelect

Author:

Zhang Hui¹²,Song Lihua¹,Yuan Weicheng³,Zhang Xiaomei³

Affiliation:

1. Department of Pharmacy Changzhi Medical College Changzhi 046000 P. R. of China

2. Science and Technology Center Shanxi Zhendong Pharmaceutical Co., Ltd. Changzhi 047100 P. R. of China

3. Chengdu Institute of Organic Chemistry Chinese Academy of Sciences Chengdu 610041 P. R. of China

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/slct.202102496

Reference58 articles.

2. Synthesis and Characterization of Two Novel Oxazol-5-ones Derivatives and Their Multifunctional Properties; pH Sensitivity, Electropolymerizability and Antiproliferative Activity

3. Current Scenario of 1,3-oxazole Derivatives for Anticancer Activity

4. Synthesis of 2-Methyl-(Z)-4-(phenylimino)naphth[2,3-d]oxazol-9-one, a Monoimine Quinone with Selective Cytotoxicity toward Cancer Cells

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