Computational Studies on Biosynthetic Carbocation Rearrangements Leading to Quiannulatene: Initial Conformation Regulates Biosynthetic Route, Stereochemistry, and Skeleton Type-Reference-Cited by-同舟云学术

Computational Studies on Biosynthetic Carbocation Rearrangements Leading to Quiannulatene: Initial Conformation Regulates Biosynthetic Route, Stereochemistry, and Skeleton Type

Published:2018-10-11 Issue:45 Volume:57 Page:14752-14757
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Sato Hajime¹²^ORCID,Mitsuhashi Takaaki³,Yamazaki Mami¹^ORCID,Abe Ikuro³^ORCID,Uchiyama Masanobu³²^ORCID

Affiliation:

1. Graduate School of Pharmaceutical Sciences; Chiba University; 1-8-1 Inohana, Chuoku Chiba 260-8675 Japan

2. Cluster of Pioneering Research (CPR), Advanced Elements Chemistry Laboratory; RIKEN; 2-1 Hirosawa Wako Saitama 351-0198 Japan

3. Graduate School of Pharmaceutical Sciences; University of Tokyo; 7-3-1 Hongo Bunkyo-ku Tokyo 113-0033 Japan

Funder

Japan Society for the Promotion of Science

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/anie.201807139/fullpdf

Reference57 articles.

1. Traversing the fungal terpenome

2. Bacterial terpene cyclases

3. Structural and Chemical Biology of Terpenoid Cyclases

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