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A novel and one-pot method for synthesis of unprecedented 3,3-dimethyl-2-amide indoles under metal-free conditions
被引:7
作者:
Liu, Haidong
[1
,3
,4
]
Chen, Hao
[2
]
Li, Yuan
[2
]
Lv, Yongfeng
[2
]
Cai, Jin
[2
]
Ji, Min
[1
,3
,4
]
机构:
[1] Southeast Univ, Sch Biol Sci & Med Engn, Nanjing 210096, Jiangsu, Peoples R China
[2] Southeast Univ, Sch Chem & Chem Engn, Nanjing 210096, Jiangsu, Peoples R China
[3] Suzhou Key Lab Biomat & Technol, Suzhou 215123, Peoples R China
[4] Collaborat Innovat Ctr Suzhou Nano Sci & Technol, Suzhou 215123, Peoples R China
关键词:
Indoles;
Iodine-promoted reaction;
1,2,3,3-Tetramethyl-3H-indolium iodide;
One-pot;
Oxidative amidation;
BISINDOLE ALKALOIDS;
ALPHA-KETOAMIDES;
FACILE ACCESS;
IODINE;
FUNCTIONALIZATION;
ACETOPHENONES;
CONSTRUCTION;
AMIDATION;
AMINATION;
STRATEGY;
D O I:
10.1016/j.tetlet.2015.03.087
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
A novel and efficient method for the synthesis of 3,3-dimethyl-2-amide indoles, employing a I-2/DMSO-promoted oxidative amidation reaction between 1,2,3,3-tetramethyl-3H-indolium iodide and cyclic secondary amines under metal-free conditions has been developed. (C) 2015 Elsevier Ltd. All rights reserved.
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页码:2332 / 2335
页数:4
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