Literature DB >> 27007992

Amitorines A and B, Nitrogenous Diterpene Metabolites of Theonella swinhoei: Isolation, Structure Elucidation, and Asymmetric Synthesis.

Koichiro Ota1, Yukiko Hamamoto1, Wakiko Eda1, Kenta Tamura1, Akiyoshi Sawada1, Ayako Hoshino1, Hidemichi Mitome2, Kazuo Kamaike1, Hiroaki Miyaoka1.   

Abstract

Two new nitrogenous prenylbisabolanes never before found in Lithistid sponges have been isolated from Theonella swinhoei. These new diterpenes, named amitorine A (1) and amitorine B (2), containing a prenylbisabolane skeleton have been characterized by spectroscopic analyses, and the relative and absolute configurations of 1 and 2 were determined by asymmetric synthesis of both diastereomers via the common bicyclic lactone 6 intermediate.

Entities:  

Mesh:

Substances:

Year:  2016        PMID: 27007992     DOI: 10.1021/acs.jnatprod.5b01069

Source DB:  PubMed          Journal:  J Nat Prod        ISSN: 0163-3864            Impact factor:   4.050


  1 in total

1.  Flow Chemistry-Enabled Divergent and Enantioselective Total Syntheses of Massarinolin A, Purpurolides B, D, E, 2,3-Deoxypurpurolide C, and Structural Revision of Massarinolin A.

Authors:  Ye-Cheng Wang; Chengsen Cui; Mingji Dai
Journal:  Angew Chem Int Ed Engl       Date:  2021-09-15       Impact factor: 15.336

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.