Regioselective C2 Sulfonylation of Indoles Mediated by Molecular Iodine-Reference-Cited by-同舟云学术

Regioselective C2 Sulfonylation of Indoles Mediated by Molecular Iodine

Published:2014-02-06 Issue:4 Volume:79 Page:1778-1785
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Katrun Praewpan¹,Mueangkaew Charoensak¹,Pohmakotr Manat¹,Reutrakul Vichai¹,Jaipetch Thaworn²,Soorukram Darunee¹,Kuhakarn Chutima¹

Affiliation:

1. Department of Chemistry and Center of Excellence for Innovation in Chemistry (PERCH-CIC), Faculty of Science, Mahidol University, Rama VI Road, Bangkok 10400, Thailand

2. Mahidol University, Kanchanaburi Campus, Saiyok, Kanchanaburi 71150, Thailand

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo402831k

Reference59 articles.

1. Indole alkaloids in medicine

2. cSeigler, D. S.Plant Secondary Metabolism;Springer:New York, 2001; pp628–667.

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

4. Gluco-indole Alkaloids from Nauclea cadamba in Thailand and Transformation of 3.ALPHA.-Dihydrocadambine into the Indolopyridine Alkaloid, 16-Carbomethoxynaufoline.

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