Hetero Diels-Alder Reaction and Ene Reaction of Acylnitroso Species in situ Generated by Hypoiodite Catalysis-Reference-Cited by-同舟云学术

Hetero Diels-Alder Reaction and Ene Reaction of Acylnitroso Species in situ Generated by Hypoiodite Catalysis

Published:2018-10-29 Issue:45 Volume:2018 Page:6199-6203
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Uraoka Saki¹,Shinohara Ikumi¹,Shimizu Hisato¹,Noguchi Keiichi²,Yoshimura Akira³⁴^ORCID,Zhdankin Viktor V.³⁴^ORCID,Saito Akio¹^ORCID

Affiliation:

1. Division of Applied Chemistry; Institute of Engineering; Tokyo University of Agriculture and Technology; 2-24-16 Naka-cho, Koganei 184-8588 Tokyo Japan

2. Instrumentation Analysis Center; Institute of Engineering; Tokyo University of Agriculture and Technology; Tokyo Japan

3. Department of Chemistry and Biochemistry; Institute of Engineering; University of Minnesota Duluth; 55812 Duluth MN USA

4. Institute of Engineering; The Tomsk Polytechnic University; 634050 Tomsk Russia

Funder

Japan Society for the Promotion of Science

Tomsk Polytechnic University

Russian Science Foundation

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ejoc.201801340/fullpdf

Reference93 articles.

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

2. Hetero-Diels-Alder-Reaktionen von Nitrosocarbonylverbindungen als nützliches Verfahren in der organischen Synthese

3. Stereo- and regioselectivity of the hetero-Diels–Alder reaction of nitroso derivatives with conjugated dienes

4. The Nitroso Ene Reaction: A Regioselective and Stereoselective Allylic Nitrogen Functionalization of Mechanistic Delight and Synthetic Potential

5. Synthesis of Acylnitroso Intermediates and Their Synthetic Applications

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