Short Synthesis of Berkeleyamide D and Determination of the Absolute Configuration by the Vibrational Circular Dichroism Exciton Chirality Method-Reference-Cited by-同舟云学术

Short Synthesis of Berkeleyamide D and Determination of the Absolute Configuration by the Vibrational Circular Dichroism Exciton Chirality Method

Published:2014-02-14 Issue:5 Volume:16 Page:1386-1389
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Komori Kenta¹,Taniguchi Tohru²,Mizutani Shoma¹,Monde Kenji²,Kuramochi Kouji¹,Tsubaki Kazunori¹

Affiliation:

1. Graduate School for Life and Environmental Sciences, Kyoto Prefectural University, 1-5 Shimogamo Hangi-cho, Sakyo-ku, Kyoto 606-8522, Japan

2. Faculty of Advanced Life Science, Frontier Research Center for Post-Genome Science and Technology, Hokkaido University, Kita 21 Nishi 11, Sapporo 001-0021, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol500148g

Reference25 articles.

1. The Berkeleyamides, Amides from the Acid Lake Fungus Penicillum rubrum

2. Pseurotin, a New Metabolite ofPseudeurotium ovalis STOLK Having an Unusual Hetero-Spirocyclic System. (Preliminary Communication)

3. The Crystal and Molecular Structure of 12, 13-Dibromopseurotin

4. Isolation and Structure of Pseurotin A, a Microbial Metabolite ofPseudeurotium ovalis STOLK with an Unusual Heterospirocyclic System

5. Azaspirene: A Novel Angiogenesis Inhibitor Containing a 1-Oxa-7-azaspiro[4.4]non-2-ene-4,6-dione Skeleton Produced by the Fungus Neosartorya sp.

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