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Recent Advances in Phosphine-Promoted (4+1) Annulation Reactions
被引:30
|作者:
Zhang, Heng
[1
]
Zhou, Rong
[1
]
机构:
[1] Taiyuan Univ Technol, Coll Chem & Chem Engn, Taiyuan 030024, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Phosphine;
Annulation;
Homogeneous catalysis;
Reaction mechanisms;
Heterocycles;
BAYLIS-HILLMAN CARBONATES;
REDUCTIVE 1+4 ANNULATION;
O-QUINONE METHIDES;
ALPHA-KETO ESTERS;
ACCESS;
MALEIMIDES;
ISATINS;
REARRANGEMENT;
CONDENSATION;
DERIVATIVES;
D O I:
10.1002/ejoc.202000023
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
Over the past two decades, the nucleophilic phosphine catalysis has effected many powerful annulation reactions and emerged as an intriguing platform for the generation of highly functionalized carbo- and heterocycles. In addition to the well-established (3 + 2) annulation, the phosphine-promoted (4 + 1) annulation has received increasing attention and developed rapidly in recent years, which complements the (3 + 2) annulation and also provides an alternative approach to structurally diverse five-membered carbo- and heterocycles. This minireview summarizes the recent advances in phosphine-promoted (4 + 1) annulation reactions according to the type of substrates used in the annulations.
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页码:4098 / 4107
页数:10
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