Total Synthesis of Aplydactone by a Conformationally Controlled C−H Functionalization-Reference-Cited by-同舟云学术

Total Synthesis of Aplydactone by a Conformationally Controlled C−H Functionalization

Published:2017-05-23 Issue:28 Volume:56 Page:8187-8190
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Liu Chenguang¹,Chen Renzhi¹,Shen Yang¹,Liang Zhanhao¹,Hua Yuhui¹,Zhang Yandong¹^ORCID

Affiliation:

1. Department of Chemistry and Key Laboratory for Chemical Biology of Fujian Province; Collaborative Innovation Center of Chemistry for Energy Materials, College of Chemistry and Chemical Engineering; Xiamen University; Xiamen Fujian 361005 China

Funder

National Natural Science Foundation of China

FRFCU

NFFTBS

NCETFJ

Publisher

Wiley

Subject

General Chemistry,Catalysis

Reference53 articles.

1. Aplydactone, a New Sesquiterpenoid with an Unprecedented Carbon Skeleton from the Sea Hare Aplysia dactylomela, and Its Cargill-Like Rearrangement

2. Novel rearrangement of 5,6-disubstituted bicyclo[4.2.0]octan-2-ones with aluminum chloride. Application to total synthesis of (.+-.)-5-oxosilphiperfol-6-ene and (.+-.)-silphiperfol-6-ene

3. Stereoelectronic effects in the cationic rearrangements of [4.3.2]propellanes

4. Total synthesis of (.+-.)-isocomene

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