Construction of Chiral Tetrahydro-β-Carbolines: Asymmetric Pictet-Spengler Reaction of Indolyl Dihydropyridines-Reference-Cited by-同舟云学术

Construction of Chiral Tetrahydro-β-Carbolines: Asymmetric Pictet-Spengler Reaction of Indolyl Dihydropyridines

Published:2017-05-23 Issue:26 Volume:56 Page:7440-7443
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Wang Shou-Guo¹,Xia Zi-Lei¹,Xu Ren-Qi¹,Liu Xi-Jia¹,Zheng Chao¹,You Shu-Li¹²^ORCID

Affiliation:

1. State Key Laboratory of Organometallic Chemistry; Shanghai Institute of Organic Chemistry; University of Chinese Academy of Sciences, Chinese Academy of Sciences; 345 Lingling Lu Shanghai 200032 China

2. Collaborative Innovation Center of Chemical Science and Engineering; Tianjin 300072 China

Funder

Ministry of Science and Technology of the People's Republic of China

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry,Catalysis

Reference83 articles.

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2. Simple indole alkaloids and those with a nonrearranged monoterpenoid unit

3. Chemistry and biology of monoterpene indole alkaloid biosynthesis

4. General Approach for the Synthesis of Sarpagine Indole Alkaloids. Enantiospecific Total Synthesis of (+)-Vellosimine, (+)-Normacusine B, (−)-Alkaloid Q3, (−)-Panarine, (+)-Na-Methylvellosimine, and (+)-Na-Methyl-16-epipericyclivine

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