Oxidative rearrangement of malondialdehyde: substrate scope and mechanistic insights-Reference-Cited by-同舟云学术

Oxidative rearrangement of malondialdehyde: substrate scope and mechanistic insights

Published:2014 Issue:96 Volume:4 Page:53397-53401
ISSN:2046-2069
Container-title:RSC Adv.
language:en
Short-container-title:RSC Adv.

Author:

Yu Xin¹²³⁴,Liu Zheng⁵⁶⁷⁸,Xia Zilei⁹¹⁰¹¹¹²,Shen Zhigao⁹¹⁰¹¹¹²,Pan Xixian¹²³⁴,Zhang Hui¹²³⁴,Xie Weiqing⁵⁶⁷⁸

Affiliation:

1. Department of Chemistry

2. School of Science & Instrumental Analysis and Research Center

3. Shanghai University

4. Shanghai 200444, China

5. State Key Laboratory of Bioorganic & Natural Products Chemistry

6. Shanghai Institute of Organic Chemistry

7. Chinese Academy of Sciences

8. Shanghai 200032, China

9. State Key Laboratory of Natural Medicines

10. Center of Drug Discovery

11. China Pharmaceutical University

12. Nanjing 210009, China

Abstract

Interception of Criegee intermediate via tandem acetalization and fragmentation reaction provides a novel oxidative decarbonylation of malondialdehyde.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/RA/C4RA11237G

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