том 35 издание 7 страницы 501-510

Taming Reactive Phenol Tautomers and o-Quinone Methides with Transition Metals:  A Structure−Reactivity Relationship

Тип публикацииJournal Article
Дата публикации2002-05-16
scimago Q1
wos Q1
БС1
SJR5.433
CiteScore30.7
Impact factor17.7
ISSN00014842, 15204898
General Chemistry
General Medicine
Краткое описание
Quinone methides act as important intermediates in organic syntheses, as well as in chemical and biological processes; however, examples of such isolated species are scarce as a result of their high reactivity. Phenol tautomers (keto form of phenol) are also important intermediates in several organic and organometallic reactions; nevertheless, isolated complexes are rare. This Account reviews the recent progress on the synthesis and reactivity of iridium and rhodium o-quinone methide complexes as well as on iridium-mediated ortho functionalization of phenols. This reaction was at the origin of the discovery of a general synthetic procedure to prepare the first metal-stabilized o-quinone methide.
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ГОСТ |
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Amouri H., Le Bras J. Taming Reactive Phenol Tautomers and o-Quinone Methides with Transition Metals: A Structure−Reactivity Relationship // Accounts of Chemical Research. 2002. Vol. 35. No. 7. pp. 501-510.
ГОСТ со всеми авторами (до 50) Скопировать
Amouri H., Le Bras J. Taming Reactive Phenol Tautomers and o-Quinone Methides with Transition Metals: A Structure−Reactivity Relationship // Accounts of Chemical Research. 2002. Vol. 35. No. 7. pp. 501-510.
RIS |
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TY - JOUR
DO - 10.1021/ar010105m
UR - https://doi.org/10.1021/ar010105m
TI - Taming Reactive Phenol Tautomers and o-Quinone Methides with Transition Metals: A Structure−Reactivity Relationship
T2 - Accounts of Chemical Research
AU - Amouri, Hani
AU - Le Bras, Jean
PY - 2002
DA - 2002/05/16
PB - American Chemical Society (ACS)
SP - 501-510
IS - 7
VL - 35
PMID - 12118989
SN - 0001-4842
SN - 1520-4898
ER -
BibTex |
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BibTex (до 50 авторов) Скопировать
@article{2002_Amouri,
author = {Hani Amouri and Jean Le Bras},
title = {Taming Reactive Phenol Tautomers and o-Quinone Methides with Transition Metals: A Structure−Reactivity Relationship},
journal = {Accounts of Chemical Research},
year = {2002},
volume = {35},
publisher = {American Chemical Society (ACS)},
month = {may},
url = {https://doi.org/10.1021/ar010105m},
number = {7},
pages = {501--510},
doi = {10.1021/ar010105m}
}
MLA
Цитировать
Amouri, Hani, and Jean Le Bras. “Taming Reactive Phenol Tautomers and o-Quinone Methides with Transition Metals: A Structure−Reactivity Relationship.” Accounts of Chemical Research, vol. 35, no. 7, May. 2002, pp. 501-510. https://doi.org/10.1021/ar010105m.