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Methods for selective benzylic C-H oxofunctionalization of organic compounds. / Lubov, D. P.; Talsi, E. P.; Bryliakov, K. P.

In: Russian Chemical Reviews, Vol. 89, No. 6, 30.06.2020, p. 587-628.

Research output: Contribution to journal › Review article › peer-review

Harvard

Lubov, DP, Talsi, EP & Bryliakov, KP 2020, 'Methods for selective benzylic C-H oxofunctionalization of organic compounds', Russian Chemical Reviews, vol. 89, no. 6, pp. 587-628. https://doi.org/10.1070/RCR4918

APA

Lubov, D. P., Talsi, E. P., & Bryliakov, K. P. (2020). Methods for selective benzylic C-H oxofunctionalization of organic compounds. Russian Chemical Reviews, 89(6), 587-628. https://doi.org/10.1070/RCR4918

Vancouver

Lubov DP, Talsi EP, Bryliakov KP. Methods for selective benzylic C-H oxofunctionalization of organic compounds. Russian Chemical Reviews. 2020 Jun 30;89(6):587-628. doi: 10.1070/RCR4918

Author

Lubov, D. P. ; Talsi, E. P. ; Bryliakov, K. P. / Methods for selective benzylic C-H oxofunctionalization of organic compounds. In: Russian Chemical Reviews. 2020 ; Vol. 89, No. 6. pp. 587-628.

BibTeX

@article{83f09ad8246040b89fea7dc62991864b,
title = "Methods for selective benzylic C-H oxofunctionalization of organic compounds",
abstract = "The development of methods for the selective oxidation of C-H groups of organic compounds resulting in the formation of C-O bonds is a challenging problem in modern synthetic organic chemistry. Versatile methods for oxofunctionalization of these groups are currently lacking. Approaches for the oxidation of benzylic C-H groups having a relatively weak C-H bond (the homolytic dissociation energy is ≈80-90 kcal/mol) differ from the methods used for the oxidation of aliphatic and aromatic C-H groups with stronger C-H bonds. The review summarizes homogeneous catalytic and non-catalytic methods for the selective oxofunctionalization of benzylic groups of organic compounds developed in the past 40 years. Reactions involving various oxidizing agents in the presence or in the absence of transition metal compounds are considered. Putative mechanisms of selected transformations are discussed, with a particular focus on selective oxidation of various substrates. The bibliography includes 278 references.",
keywords = "TERT-BUTYL HYDROPEROXIDE, IRON-CATALYZED OXIDATION, 2-ARYLACETIC ACID-DERIVATIVES, LIGHT PHOTOREDOX CATALYSIS, AQUEOUS HYDROGEN-PEROXIDE, O-IODOXYBENZOIC ACID, AEROBIC OXIDATION, TRANSITION-METAL, NONHEME IRON, CARBONYL-COMPOUNDS",
author = "Lubov, {D. P.} and Talsi, {E. P.} and Bryliakov, {K. P.}",
year = "2020",
month = jun,
day = "30",
doi = "10.1070/RCR4918",
language = "English",
volume = "89",
pages = "587--628",
journal = "Russian Chemical Reviews",
issn = "0036-021X",
publisher = "Turpion Ltd.",
number = "6",

}

RIS

TY - JOUR

T1 - Methods for selective benzylic C-H oxofunctionalization of organic compounds

AU - Lubov, D. P.

AU - Talsi, E. P.

AU - Bryliakov, K. P.

PY - 2020/6/30

Y1 - 2020/6/30

N2 - The development of methods for the selective oxidation of C-H groups of organic compounds resulting in the formation of C-O bonds is a challenging problem in modern synthetic organic chemistry. Versatile methods for oxofunctionalization of these groups are currently lacking. Approaches for the oxidation of benzylic C-H groups having a relatively weak C-H bond (the homolytic dissociation energy is ≈80-90 kcal/mol) differ from the methods used for the oxidation of aliphatic and aromatic C-H groups with stronger C-H bonds. The review summarizes homogeneous catalytic and non-catalytic methods for the selective oxofunctionalization of benzylic groups of organic compounds developed in the past 40 years. Reactions involving various oxidizing agents in the presence or in the absence of transition metal compounds are considered. Putative mechanisms of selected transformations are discussed, with a particular focus on selective oxidation of various substrates. The bibliography includes 278 references.

AB - The development of methods for the selective oxidation of C-H groups of organic compounds resulting in the formation of C-O bonds is a challenging problem in modern synthetic organic chemistry. Versatile methods for oxofunctionalization of these groups are currently lacking. Approaches for the oxidation of benzylic C-H groups having a relatively weak C-H bond (the homolytic dissociation energy is ≈80-90 kcal/mol) differ from the methods used for the oxidation of aliphatic and aromatic C-H groups with stronger C-H bonds. The review summarizes homogeneous catalytic and non-catalytic methods for the selective oxofunctionalization of benzylic groups of organic compounds developed in the past 40 years. Reactions involving various oxidizing agents in the presence or in the absence of transition metal compounds are considered. Putative mechanisms of selected transformations are discussed, with a particular focus on selective oxidation of various substrates. The bibliography includes 278 references.

KW - TERT-BUTYL HYDROPEROXIDE

KW - IRON-CATALYZED OXIDATION

KW - 2-ARYLACETIC ACID-DERIVATIVES

KW - LIGHT PHOTOREDOX CATALYSIS

KW - AQUEOUS HYDROGEN-PEROXIDE

KW - O-IODOXYBENZOIC ACID

KW - AEROBIC OXIDATION

KW - TRANSITION-METAL

KW - NONHEME IRON

KW - CARBONYL-COMPOUNDS

UR - http://www.scopus.com/inward/record.url?scp=85086674069&partnerID=8YFLogxK

U2 - 10.1070/RCR4918

DO - 10.1070/RCR4918

M3 - Review article

AN - SCOPUS:85086674069

VL - 89

SP - 587

EP - 628

JO - Russian Chemical Reviews

JF - Russian Chemical Reviews

SN - 0036-021X

IS - 6

ER -

ID: 24566966