A short synthesis of (±)-cherylline dimethyl ether

Bhima Y. Kale; Ananta D. Shinde; Swapnil S. Sonar; Bapurao B. Shingate; Sanjeev Kumar; Samir Ghosh; Soodamani Venugopal; Murlidhar S. Shingare

Journal ArticleOPEN ACCESS

A short synthesis of (±)-cherylline dimethyl ether

Kale B
Shinde A
Sonar S
et al.

Beilstein Journal of Organic Chemistry (2009) 5

DOI: 10.3762/bjoc.5.80

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Abstract

A synthesis of (±)-cherylline dimethyl ether is reported. The key steps involved are Michael-type addition, radical azidonation of an aldehyde, Curtius rearrangement, and reduction of an isocyanate intermediate followed by Pictet-Spengler cyclization. © 2009 Kale et al; licensee Beilstein-Institut.

Author supplied keywords

Curtius rearrangement
Michael reaction
Pictet-Spengler cyclization
Radical azidonation

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APA

Kale, B. Y., Shinde, A. D., Sonar, S. S., Shingate, B. B., Kumar, S., Ghosh, S., … Shingare, M. S. (2009). A short synthesis of (±)-cherylline dimethyl ether. Beilstein Journal of Organic Chemistry, 5. https://doi.org/10.3762/bjoc.5.80

A short synthesis of (±)-cherylline dimethyl ether

Abstract

Author supplied keywords

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