Sodium-iodoxybenzoate mediated highly chemoselective aziridination of olefins-Reference-Cited by-同舟云学术

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Sodium-iodoxybenzoate mediated highly chemoselective aziridination of olefins

Published:2014-09 Issue:35 Volume:70 Page:5884-5894
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Bakthavachalam Ananthan,Chuang Hui-Chun,Yan Tu-Hsin

Funder

National Science Council of the Republic of China

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference66 articles.

1. Handbook of Natural Products;Dembitsky,2013

2. Heterocycles in Natural Product Synthesis, Part-1;Botuha,2011

3. Aziridines and Epoxides in Organic Synthesis,2006

4. Ullman's Encyclopedia of Industrial Chemistry;Steuerle,2006

5. Comprehensive Heterocyclic Chemistry III;Padwa,2008

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1. Aziridination via Nitrogen-Atom Transfer to Olefins from Photoexcited Azoxy-Triazenes;Journal of the American Chemical Society;2024-03-24

2. Aziridines and Azirines: Fused-Ring Derivatives;Comprehensive Heterocyclic Chemistry IV;2022

3. 3-Arylaziridine-2-carboxylic Acid Derivatives and (3-Arylaziridin-2-yl)ketones: The Aziridination Approaches;International Journal of Molecular Sciences;2021-09-13

4. Conformationally constrained fused bicyclic iminosugars: synthetic challenges and opportunities;Arkivoc;2019-02-20

5. Site-Selective, Catalyst-Controlled Alkene Aziridination;Synthesis;2018-07-23

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