Taming Reactive Phenol Tautomers and o-Quinone Methides with Transition Metals: A Structure−Reactivity Relationship
Тип публикации: Journal Article
Дата публикации: 2002-05-16
scimago Q1
wos Q1
БС1
SJR: 5.433
CiteScore: 30.7
Impact factor: 17.7
ISSN: 00014842, 15204898
PubMed ID:
12118989
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)
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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.
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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 -
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BibTex (до 50 авторов)
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@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}
}
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MLA
Скопировать
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.