An Experimental and Computational Approach to Understanding the Reactions of Acyl Nitroso Compounds in [4 + 2] Cycloadditions-Reference-Cited by-同舟云学术

An Experimental and Computational Approach to Understanding the Reactions of Acyl Nitroso Compounds in [4 + 2] Cycloadditions

Published:2015-09-15 Issue:19 Volume:80 Page:9518-9534
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Chaiyaveij Duangduan¹,Batsanov Andrei S.²,Fox Mark A.²,Marder Todd B.³,Whiting Andrew²

Affiliation:

1. Chemistry Department, Faculty of Science and Technology, Thammasat University Rangsit Campus, Khlongluang, Pathumthani 12120, Thailand

2. Centre for Sustainable Chemical Processes, Department of Chemistry, Durham University, Science Laboratories, South Road, Durham DH1 3LE, United Kingdom

3. Institut für Anorganische Chemie, Julius-Maximilians-Universität Würzburg, Am Hubland, 97074 Würzburg, Germany

Funder

Thammasat University

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.5b01470

Reference70 articles.

1. Nitrosobenzol und Nitrosonaphtalin

2. Tilden Lecture. Electrophilic C-nitroso-compounds

3. Development and applications of amino acid-derived chiral acylnitroso hetero Diels-Alder reactions

4. The Nitrosocarbonyl Hetero-Diels-Alder Reaction as a Useful Tool for Organic Syntheses

5. Nitroso Diels–Alder (NDA) reaction as an efficient tool for the functionalization of diene-containing natural products

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