Regio- and Stereospecific Construction of 3a-(1H-Indol-3-yl)pyrrolidinoindolines and Application to the Formal Syntheses of Gliocladins B and C
Author:
Affiliation:
1. Key Laboratory of Chemical Genomics, School of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate School, Xili, Nanshan District, Shenzhen 518055, China
Funder
National Natural Science Foundation of China
Natural Science Foundation of Guangdong Province
Shenzhen Science and Technology Innovation Committee
Shenzhen Municipality
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.7b02425
Reference30 articles.
1. Gliocladins A - C and Glioperazine ; Cytotoxic Dioxo- or Trioxopiperazine Metabolites from a Gliocladium Sp. Separated from a Sea Hare
2. Bionectins A−C, Epidithiodioxopiperazines with Anti-MRSA Activity, from Bionectra byssicola F120
3. Novel Cytotoxic Thiodiketopiperazine Derivatives from a Tilachlidium sp.
4. Nematicidal Epipolysulfanyldioxopiperazines from Gliocladium roseum
5. Leptosins, antitumour metabolites of a fungus isolated from a marine alga
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