共 65 条
Rhodium(III)-Catalyzed Intramolecular Annulation and Aromatization for the Synthesis of Pyrrolo[1,2-a]quinolines
被引:9
作者:

Hu, Yongchun
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机构:
Hunan Normal Univ, Key Lab Chem Biol & Tradit Chinese Med, Minist Educ China, Changsha 410081, Peoples R China
Hunan Normal Univ, Key Lab Assembly & Applicat Organ Funct Mol Hunan, Changsha 410081, Peoples R China Hunan Normal Univ, Key Lab Chem Biol & Tradit Chinese Med, Minist Educ China, Changsha 410081, Peoples R China

Jia, Yuanyuan
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机构:
Xiangtan Univ, Coll Chem Engn, Xiangtan 411105, Peoples R China Hunan Normal Univ, Key Lab Chem Biol & Tradit Chinese Med, Minist Educ China, Changsha 410081, Peoples R China

Tuo, Zekun
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机构:
Hunan Normal Univ, Key Lab Chem Biol & Tradit Chinese Med, Minist Educ China, Changsha 410081, Peoples R China
Hunan Normal Univ, Key Lab Assembly & Applicat Organ Funct Mol Hunan, Changsha 410081, Peoples R China Hunan Normal Univ, Key Lab Chem Biol & Tradit Chinese Med, Minist Educ China, Changsha 410081, Peoples R China

Zhou, Wang
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h-index: 0
机构:
Hunan Normal Univ, Key Lab Chem Biol & Tradit Chinese Med, Minist Educ China, Changsha 410081, Peoples R China
Hunan Normal Univ, Key Lab Assembly & Applicat Organ Funct Mol Hunan, Changsha 410081, Peoples R China
Xiangtan Univ, Coll Chem Engn, Xiangtan 411105, Peoples R China Hunan Normal Univ, Key Lab Chem Biol & Tradit Chinese Med, Minist Educ China, Changsha 410081, Peoples R China
机构:
[1] Hunan Normal Univ, Key Lab Chem Biol & Tradit Chinese Med, Minist Educ China, Changsha 410081, Peoples R China
[2] Hunan Normal Univ, Key Lab Assembly & Applicat Organ Funct Mol Hunan, Changsha 410081, Peoples R China
[3] Xiangtan Univ, Coll Chem Engn, Xiangtan 411105, Peoples R China
基金:
中国国家自然科学基金;
关键词:
PALLADIUM-CATALYZED ANNULATION;
C BOND FORMATION;
INTERNAL ALKYNES;
H ACTIVATION;
ACCESS;
FUNCTIONALIZATION;
PYRROLOQUINOLINES;
HYDROCARBONS;
CYCLIZATION;
QUINOLINES;
D O I:
10.1021/acs.orglett.3c00321
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
A rhodium(III)-catalyzed protocol for the synthesis of pyrrolo[1,2-a]quinolines through intramolecular annulation of o-alkynyl amino aromatic ketones and subsequent aromatization is reported. This transformation builds the pyrrole and quinoline moieties of the pyrrolo[1,2-a]quinoline in one pot and achieves a flexible introduction of different substituent groups at 4- and 5-positions on products that were difficult to prepare by other means. The reaction proceeds smoothly on a gram scale, and the products are amenable to downstream synthetic manipulations.
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页码:1845 / 1849
页数:5
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