Facile Creation of 2‐Substituted Indolin‐3‐ones by Using Primary–Secondary Diamine Catalysts-Reference-Cited by-同舟云学术

Facile Creation of 2‐Substituted Indolin‐3‐ones by Using Primary–Secondary Diamine Catalysts

Published:2011-04-18 Issue:22 Volume:17 Page:6030-6033
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Sun Wangsheng¹,Hong Liang¹,Wang Rui¹²

Affiliation:

1. Key Laboratory of Preclinical Study for New Drugs of Gansu Province, State Key Laboratory of Applied Organic Chemistry and Institute of Biochemistry and Molecular Biology, Lanzhou University, Lanzhou, 730000 (P.R. China), Fax: (+86) 931‐891‐2567

2. State Key Laboratory of Chiroscience and Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Kowloon (Hong Kong)

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.201100144

Reference109 articles.

2. A Short Synthetic Route to (+)-Austamide, (+)-Deoxyisoaustamide, and (+)-Hydratoaustamide from a Common Precursor by a Novel Palladium-Mediated Indole → Dihydroindoloazocine Cyclization

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

4. Total synthesis of (-)-alloaristoteline, (-)-serratoline, and (+)-aristotelone

5. Total Synthesis of (+)-Isatisine A

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