共 183 条
The Paterno-Buchi reaction-Mechanisms and application to organic synthesis
被引:89
作者:
Freneau, Maxime
[1
]
Hoffmann, Norbert
[1
]
机构:
[1] Univ Reims, CNRS, ICMR, Equipe Photochim,UFR Sci, BP 1039, F-51687 Reims, France
关键词:
Photocycloadditions;
Oxetanes;
Reaction mechanism;
Stereoselectivity;
Organic synthesis;
CARBONYL PHOTOCYCLOADDITION REACTION;
ARENECARBOXYLIC ACID-ESTERS;
2+2 CYCLO-ADDITION;
N-ACYL ENAMINES;
PHOTOCHEMICAL-REACTIONS;
OXETANE FORMATION;
CHIRAL INDUCTION;
HYDROGEN ABSTRACTION;
ELECTRON-TRANSFER;
FACIAL DIASTEREOSELECTIVITY;
D O I:
10.1016/j.jphotochemrev.2017.10.002
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
The [2+2] photocycloaddition between an electronically excited carbonyl compound and an alkene leading to oxetanes (Paterno-Buchi reaction) is one of the most investigated organic photochemical reaction. Regio-, stereo- and site selectivities are discussed as a consequence of the reaction mechanism. Spin multiplicity and electron transfer have a significant impact on the outcome of the reaction. Typical carbonyl and alkene reaction partners are presented indicating scope and limitation of the reaction. The Paterno-Buchi reaction possesses particular interest for being applied to organic synthesis, considering the difficulty for non-photochemical reactions to obtain oxetanes, with or without stereoselectivity. Mechanistic details are particularly focused. It has been applied as key step in various multi-step syntheses. (C) 2017 Elsevier B.V. All rights reserved.
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页码:83 / 108
页数:26
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