Oxyfunctionalization of Non-Natural Targets by Dioxiranes. 4.1 Efficient Oxidation of Binor S Using Methyl(trifluoromethyl)dioxirane-Reference-Cited by-同舟云学术

Oxyfunctionalization of Non-Natural Targets by Dioxiranes. 4.1 Efficient Oxidation of Binor S Using Methyl(trifluoromethyl)dioxirane

Published:2001-11-22 Issue:26 Volume:66 Page:9063-9066
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

D'Accolti Lucia¹,Fusco Caterina¹,Lucchini Vittorio¹,Carpenter Gene B.¹,Curci Ruggero¹

Affiliation:

1. Centro C.N.R. “M.I.S.O.”, Dipartimento Chimica, Università di Bari, v. Amendola 173, I-70126 Bari, Italy, the Chemistry Department, Brown University, Providence, Rhode Island 02912, and the Dipartimento Scienze Ambientali, University of Venice, Dorsoduro 2137, I-30123 Venice, Italy csmirc17@area.ba.cnr.it

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0109671

Reference26 articles.

1. Oxyfunctionalization of Non-Natural Targets by Dioxiranes. 3.1 Efficient Oxidation of Buckminsterfullerene C60 with Methyl(trifluoromethyl)dioxirane

2. Dioxirane oxidations: Taming the reactivity-selectivity principle

3. Dioxiranes: synthesis and reactions of methyldioxiranes

4. Oxidations by methyl(trifluoromethyl)dioxirane. 2. Oxyfunctionalization of saturated hydrocarbons

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