Stereoelectronic power of oxygen in control of chemical reactivity: the anomeric effect is not alone-Reference-Cited by-同舟云学术

Stereoelectronic power of oxygen in control of chemical reactivity: the anomeric effect is not alone

Published:2021 Issue:18 Volume:50 Page:10253-10345
ISSN:0306-0012
Container-title:Chemical Society Reviews
language:en
Short-container-title:Chem. Soc. Rev.

Author:

Alabugin Igor V.¹^ORCID,Kuhn Leah¹^ORCID,Medvedev Michael G.²³^ORCID,Krivoshchapov Nikolai V.²⁴^ORCID,Vil’ Vera A.²^ORCID,Yaremenko Ivan A.²^ORCID,Mehaffy Patricia¹,Yarie Meysam⁵^ORCID,Terent’ev Alexander O.²^ORCID,Zolfigol Mohammad Ali⁵^ORCID

Affiliation:

1. Department of Chemistry and Biochemistry, Florida State University, Tallahassee, FL 32306, USA

2. N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991 Moscow, Russian Federation

3. A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 Vavilova St., 119991 Moscow, Russian Federation

4. Lomonosov Moscow State University, Leninskie Gory 1 (3), Moscow, 119991, Russian Federation

5. Department of Organic Chemistry, Faculty of Chemistry, Bu-Ali Sina University, Hamedan 65167, Iran

Abstract

The chameleonic properties of oxygen accounts for the diverse reactivity of O-functionalities and their profound role in organic synthesis.

Funder

Division of Chemistry

Russian Science Foundation

Ministry of Science and Higher Education of the Russian Federation

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/CS/D1CS00386K

Reference452 articles.

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2. Intramolecular strategies and stereoelectronic effects. Glycosides hydrolysis revisited

3. A revision of the value for the anomeric effect

4. The anomeric effect with central atoms other than carbon. 2. Strong interactions between nonbonded substituents in mono- and polyfluorinated first- and second-row amines, FnAHmNH2

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