Carboxylate phosphabetaine as a bifunctional organocatalyst for the intramolecular ring opening of oxetane-Reference-Cited by-同舟云学术

Carboxylate phosphabetaine as a bifunctional organocatalyst for the intramolecular ring opening of oxetane

Published:2019 Issue:10 Volume:6 Page:1681-1685
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Xu Dongyang¹²³⁴⁵,Wei Hongbo¹²³⁴⁵,Zhen Yanxia¹²³⁴⁵,Gao Yu-Qi¹²³⁴⁵,Li Ruoxin¹²³⁴⁵,Li Xingzhou⁶⁷⁸⁹,He Yupeng¹⁰¹¹¹²¹³⁵,Zhang Zhong¹²³⁴⁵,Xie Weiqing¹²³⁴⁵^ORCID

Affiliation:

1. Shaanxi Key Laboratory of Natural Products & Chemical Biology

2. College of Chemistry & Pharmacy

3. Northwest A&F University

4. Yangling 712100

5. China

6. Laboratory of Computer-Aided Drug Design & Discovery

7. Beijing Institute of Pharmacology and Toxicology

8. Beijing 100850

9. P.R. China

10. College of Chemistry

11. Chemical Engineering and Environmental Engineering

12. Liaoning Shihua University

13. Fushun 113001

Abstract

Carboxylate phosphabetaine acts as a competent organocatalyst for promoting the intramolecular ring opening of oxetanes.

Funder

National Natural Science Foundation of China

Chinese Universities Scientific Fund

Northwest A and F University

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/QO/C9QO00304E

Reference46 articles.

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3. R. Mahrwald , Enantioselective organocatalyzed reactions I , Springer , 2011

4. R. Mahrwald , Enantioselective organocatalyzed reactions, II : asymmetric C-C bond formation processes , Springer , 2011

5. C. Ballester , J.Castel , L.Testi , D. S.Intrigliolo and J. R.Castel , Comprehensive enantioselective organocatalysis , Wiley-VCH , 2013

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