Synthesis Of Biologically Active Bis(Indolyl)Methane Derivatives by Bisindole Alkylation of Tetrahydroisoquinolines with Visible‐Light Induced Ring‐Opening Fragmentation.-Reference-Cited by-同舟云学术

Synthesis Of Biologically Active Bis(Indolyl)Methane Derivatives by Bisindole Alkylation of Tetrahydroisoquinolines with Visible‐Light Induced Ring‐Opening Fragmentation.

Published:2016-10-13 Issue:4 Volume:6 Page:426-431
ISSN:2193-5807
Container-title:Asian Journal of Organic Chemistry
language:en
Short-container-title:Asian J. Org. Chem.

Author:

Chen Chia‐Chueng¹,Hong Bor‐Cherng¹^ORCID,Li Wen‐Shan²,Chang Tzu‐Ting²,Lee Gene‐Hsiang³

Affiliation:

1. Department of Chemistry and BiochemistryNational Chung Cheng University 168 University Rd. Chia-Yi 621, Taiwan R.O.C.

2. Institute of ChemistryAcademia Sinica No. 128, Sec. 2, Academia Rd., Nankang Taipei 115, Taiwan R.O.C.

3. Instrumentation CenterNational Taiwan University No 1, Sec 4, Roosevelt Rd. Taipei 106, Taiwan R.O.C.

Funder

Ministry of Science and Technology, Taiwan

Publisher

Wiley

Subject

Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajoc.201600415

Reference95 articles.

2. Bis- and Trisindolylmethanes (BIMs and TIMs)†

3. Bis(indolyl)methane Alkaloids: Isolation, Bioactivity, and Syntheses

5. Indole alkaloids from Balansia epichloe (Weese)

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