Highly Diastereoselective Synthesis of Polycyclic Indolines through Formal [4+2] Propargylic Cycloaddition of Indoles with Ethynyl Benzoxazinanones-Reference-Cited by-同舟云学术

Highly Diastereoselective Synthesis of Polycyclic Indolines through Formal [4+2] Propargylic Cycloaddition of Indoles with Ethynyl Benzoxazinanones

Published:2020-07-10 Issue:16 Volume:15 Page:2462-2466
ISSN:1861-4728
Container-title:Chemistry – An Asian Journal
language:en
Short-container-title:Chem. Asian J.

Author:

Shao Wen¹,Xu‐Xu Qing‐Feng¹,You Shu‐Li¹^ORCID

Affiliation:

1. State Key Laboratory of Organometallic ChemistryCenter for Excellence in Molecular SynthesisShanghai Institute of Organic ChemistryUniversity of Chinese Academy of SciencesChinese Academy of Sciences 345 Lingling Lu Shanghai 200032 China

Funder

National Basic Research Program of China

National Natural Science Foundation of China

Program of Shanghai Subject Chief Scientist

Publisher

Wiley

Subject

General Chemistry,Biochemistry,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/asia.202000640

Reference120 articles.

2. Naturally Occurring Cyclotryptophans and Cyclotryptamines

3. Isolation and Synthesis of Biologically Active Carbazole Alkaloids

4. Construction of Spiro[pyrrolidine‐3,3′‐oxindoles] − Recent Applications to the Synthesis of Oxindole Alkaloids

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