Computational study on the mechanism of uncatalyzed and selenium-based catalyzed bromolactonization-Reference-Cited by-同舟云学术

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Computational study on the mechanism of uncatalyzed and selenium-based catalyzed bromolactonization

Published:2014-10 Issue: Volume:1046 Page:49-56
ISSN:2210-271X
Container-title:Computational and Theoretical Chemistry
language:en
Short-container-title:Computational and Theoretical Chemistry

Author:

Sun Chuanzhi,He Xiaodan,Wang Wenjuan,Chu Guohong,Zhang Shuxiang,Chen Dezhan

Funder

National Natural Science Foundations of China

Advanced School Program of Science and Technology of Shandong Province

Publisher

Elsevier BV

Subject

Physical and Theoretical Chemistry,Condensed Matter Physics,Biochemistry

Reference40 articles.

1. Organocatalytic asymmetric halogenation/semipinacol rearrangement: highly efficient synthesis of chiral α-oxa-quaternary β-haloketones;Chen;J. Am. Chem. Soc.,2011

2. Total synthesis, relay synthesis, and structural confirmation of the C18-norditerpenoid alkaloid neofinaconitine;Shi;J. Am. Chem. Soc,2013

3. A unified strategy to ent-kauranoid natural products: total syntheses of (−)-trichorabdal A and (−)-Longikaurin E;Yeoman;J. Am. Chem. Soc,2013

4. Structure of shikodonin, a unique anti-tumor spirosecokaurene diterpenoid;Kubo;J. Am. Chem. Soc.,1978

5. Terpenoids. LIII. antitumor activity of trichorabdals and related compounds;Fuji;Chem. Pharm. Bull.,1989

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