Issue 43, 2014
From the journal:

RSC Advances

First example of a Prins–Ritter reaction on terpenoids: a diastereoselective route to novel 4-amido-octahydro-2H-chromenes†

Barnali Sarmah,a   Gakul Baishya*a  and  Rajani K. Baruahb  

* Corresponding authors

a Natural Products Chemistry Division, CSIR-North East Institute of Science & Technology, Jorhat-785006, India
E-mail: b.gakul@gmail.com
Fax: +91-376-2370011

b Analytical Chemistry Division, CSIR-North East Institute of Science & Technology, Jorhat-785006, India
Fax: +91-376-2370011

Abstract

(−)-Isopulegol was subjected to a triflic acid-promoted three-component Prins–Ritter reaction with a series of aldehydes to produce a library of novel 4-acetamido-octahydro-2H-chromene derivatives in good yields and high diastereoselectivities.

Graphical abstract: First example of a Prins–Ritter reaction on terpenoids: a diastereoselective route to novel 4-amido-octahydro-2H-chromenes

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Article information

DOI
https://doi.org/10.1039/C4RA02124J
Article type
Paper
Submitted
11 Mar 2014
Accepted
28 Apr 2014
First published
29 Apr 2014

RSC Adv., 2014,4, 22387-22397

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First example of a Prins–Ritter reaction on terpenoids: a diastereoselective route to novel 4-amido-octahydro-2H-chromenes

B. Sarmah, G. Baishya and R. K. Baruah, RSC Adv., 2014, 4, 22387 DOI: 10.1039/C4RA02124J

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