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One-Pot Synthesis of 3-Iminoisoindolinones by a Rhodium(III)-Catalyzed and Methanol-Assisted C-H Cyanation-Cyclization Cascade with N-Alkoxyl Transfer
被引:12
|作者:
Jia, Jinlong
[1
]
Liu, Xuelei
[1
]
Shi, Jingjing
[1
]
Xu, H. Eric
[1
,2
]
Yi, Wei
[1
]
机构:
[1] Chinese Acad Sci, Shanghai Inst Mat Medica, Ctr Struct & Funct Drug Targets, VARI SIMM Ctr,Key Lab Receptor Res, Shanghai 201203, Peoples R China
[2] Van Andel Res Inst, Lab Struct Sci, Program Struct Biol & Drug Discovery, Grand Rapids, MI 49503 USA
关键词:
C-H functionalization;
3-iminoisoindolinones;
N-alkoxybenzamides;
N-cyano-N-phenyl-p-toluenesulfonamide;
rhodium;
PHENYL-P-TOLUENESULFONAMIDE;
BOND FUNCTIONALIZATIONS;
ISOINDOLINE DYES;
ACTIVATION;
ARENES;
OXIDES;
HETEROCYCLES;
INDOLES;
ALKYNES;
D O I:
10.1002/ajoc.201500294
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
Herein, we disclose the Rh-III-catalyzed and MeOH-assisted direct C-H functionalization of simple N-alkoxybenzamides with N-cyano-N-phenyl-p-toluenesulfonamide (NCTS) in a one-pot cascade synthesis of 3-iminoisoindolinones with excellent substrate/functional group tolerance. Experimental studies reveal that the versatile reaction comprises a regioselective C-H cyanation and subsequent intramolecular cyclization along with N-alkoxyl transfer. Furthermore, the synthetic application of the obtained products to rapidly build other important structural motifs, such as lactams and phthalazinones, has also been demonstrated in subsequent derivatization reactions.
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页码:1250 / 1253
页数:4
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