Chemoenzymatic Synthesis of (+)-Asperpentyn and the Enantiomer of the Structure Assigned to Aspergillusol A-Reference-Cited by-同舟云学术

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Chemoenzymatic Synthesis of (+)-Asperpentyn and the Enantiomer of the Structure Assigned to Aspergillusol A

Published:2015-08-13 Issue:8 Volume:78 Page:1963-1968
ISSN:0163-3864
Container-title:Journal of Natural Products
language:en
Short-container-title:J. Nat. Prod.

Author:

Lan Ping¹,White Lauren E.¹,Taher Ehab S.¹,Guest Prudence E.¹,Banwell Martin G.¹,Willis Anthony C.¹

Affiliation:

1. Research School of Chemistry, Institute of Advanced Studies, The Australian National University, Canberra, ACT 2601, Australia

Funder

Islamic Development Bank

China Scholarship Council

Australian Research Council

Institute of Advanced Studies, Australian National University

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Complementary and alternative medicine,Drug Discovery,Pharmaceutical Science,Pharmacology,Molecular Medicine,Analytical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.jnatprod.5b00304

Reference33 articles.

1. γ-Butyrolactone, Cytochalasin, Cyclic Carbonate, Eutypinic Acid, and Phenalenone Derivatives from the Soil Fungus Aspergillus sp. PSU-RSPG185

2. Indole-benzodiazepine-2,5-dione derivatives from a soil fungus Aspergillus sp. PSU-RSPG185

3. A cyclic carbonate and related polyketides from a marine-derived fungus of the genus Phoma

4. Phomoxins B and C: Polyketides from an endophytic fungus of the genus Eupenicillium

5. Asperpentyn, a novel acetylenic cyclohexene epoxide from Aspergillus duricaulis

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