Total Synthesis of Notoamides F, I, and R and Sclerotiamide-Reference-Cited by-同舟云学术

Total Synthesis of Notoamides F, I, and R and Sclerotiamide

Published:2016-07-22 Issue:35 Volume:128 Page:10591-10594
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angew. Chem.

Author:

Zhang Benxiang¹,Zheng Weifeng¹,Wang Xiaoqing¹,Sun Deqian¹,Li Chaozhong¹²^ORCID

Affiliation:

1. Key Laboratory of Organofluorine Chemistry and Collaborative Innovation Center of Chemistry for Life Sciences; Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences; 345 Lingling Road Shanghai 200032 P.R. China

2. School of Chemical Engineering; Ningbo University of Technology; 89 Cuibai Road Ningbo 315016 P.R. China

Funder

NSFC

Publisher

Wiley

Subject

General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ange.201604754/fullpdf

Reference51 articles.

1. Synthetic approaches to the bicyclo[2.2.2]diazaoctane ring system common to the paraherquamides, stephacidins and related prenylated indole alkaloids

2. Facial selectivity of the intramolecular SN2' cyclization: stereocontrolled total synthesis of brevianamide B

3. Asymmetric, stereocontrolled total synthesis of (-)-brevianamide B

4. A concise synthesis of d,l-brevianamide B via a biomimetically-inspired IMDA construction

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