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Alkene Synthesis Through Transition Metal-Catalyzed Cross-Coupling of N-Tosylhydrazones
被引:67
作者:
Zhang, Yan
[1
]
Wang, Jianbo
[1
]
机构:
[1] Peking Univ, BNLMS, Key Lab Bioorgan Chem & Mol Engn, Minist Educ,Coll Chem, Beijing 100871, Peoples R China
来源:
STEREOSELECTIVE ALKENE SYNTHESIS
|
2012年
/
327卷
关键词:
Alkene synthesis;
Cross-coupling;
Metal carbene;
N-Tosylhydrazones;
ARYL HALIDES SYNTHESIS;
C=C BOND FORMATION;
CARBENE INSERTION;
STEREOSELECTIVE-SYNTHESIS;
DIAZO-COMPOUNDS;
SELECTIVE OLEFINATION;
ORGANOMETALLIC ANALOG;
CARBONYL-COMPOUNDS;
VINYL HALIDES;
ALPHA-HYDROXY;
D O I:
10.1007/128_2012_322
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
In this chapter, alkene synthesis based on the reaction of N-tosylhydrazones is described. The reactivity of tosylhydrazones is determined by either the acidity of alpha-proton and hydrazone proton or the electropositivity of the carbon of C-N bond. This leads to diverse reactivities and a series of N-tosylhydrazone-based olefination methodologies. Both non-catalytic and transition metal-catalyzed olefinations from N-tosylhydrazones are introduced in this chapter. Most of the transition metal-catalyzed reactions proceed via metal carbene transformations. The synthesis of alkenes through Pd-catalyzed cross-coupling reactions of N-tosylhydrazones is particularly attractive and will be discussed in detail.
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页码:239 / 269
页数:31
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