Issue 69, 2015

Direct access to functionalized 4-nitromethyl-chromenes via a domino reaction under catalyst-free conditions

Abstract

A catalyst-free tandem reaction for synthesis of 4-nitromethyl-chromenes has been established from accessible α,β-unsaturated ketones and CH3NO2. Target products were obtained in non-toxic solvent under catalyst-free conditions. Especially, the scope of substrates was expanded to tricyclic α,β-unsaturated ketones for the synthesis of tetracyclic heterocompounds in medium to good yields.

Graphical abstract: Direct access to functionalized 4-nitromethyl-chromenes via a domino reaction under catalyst-free conditions

Supplementary files

Article information

Article type
Paper
Submitted
14 Jun 2015
Accepted
22 Jun 2015
First published
22 Jun 2015

RSC Adv., 2015,5, 56333-56336

Author version available

Direct access to functionalized 4-nitromethyl-chromenes via a domino reaction under catalyst-free conditions

W. Xu, Q. Li, W. Wang, H. Zheng, F. Zhang and Y. Hu, RSC Adv., 2015, 5, 56333 DOI: 10.1039/C5RA11333D

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