Issue 80, 2016, Issue in Progress
From the journal:

RSC Advances

Caveat in the stereochemical outcome of the organocatalytic Diels–Alder reaction in PEG-400†

Pantapalli M. Anitha,a   Prathama S. Mainkar,*a   Shivakrishna Kallepu,a   V. S. Phani Babu,b   Cirandur Suresh Reddyc  and  Srivari Chandrasekhar*a  

* Corresponding authors

a Division of Natural Product Chemistry, CSIR-Indian Institute of Chemical Technology, Hyderabad 500007, India
E-mail: srivaric@iict.res.in

b Centre for NMR and Structural Chemistry, CSIR-Indian Institute of Chemical Technology, Hyderabad 500007, India

c Department of Chemistry, Sri Venkateswara University, Tirupati, India

Abstract

The organocatalytic Diels–Alder reaction in non-conventional solvent (PEG-400) has yielded cycloaddition products with diastereoselectivities hitherto not reported in detail using classical reaction conditions.

Graphical abstract: Caveat in the stereochemical outcome of the organocatalytic Diels–Alder reaction in PEG-400

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Article information

DOI
https://doi.org/10.1039/C6RA15035G
Article type
Communication
Submitted
09 Jun 2016
Accepted
01 Aug 2016
First published
02 Aug 2016

RSC Adv., 2016,6, 76132-76136

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Caveat in the stereochemical outcome of the organocatalytic Diels–Alder reaction in PEG-400

P. M. Anitha, P. S. Mainkar, S. Kallepu, V. S. P. Babu, C. S. Reddy and S. Chandrasekhar, RSC Adv., 2016, 6, 76132 DOI: 10.1039/C6RA15035G

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