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Rh(III)-Catalyzed Chemoselective [4+2] Annulations for the Synthesis of [1,3]Oxazinoindolones: A Combined Experimental and Computational Study
被引:2
作者:

Kumar, Perla Bharath
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Indian Inst Chem Technol, Fluoro & Agrochem Div, CSIR, Hyderabad 500007, India
Acad Sci & Innovat Res, Ghaziabad 201002, India Indian Inst Chem Technol, Fluoro & Agrochem Div, CSIR, Hyderabad 500007, India

Raju, Chittala Emmaniel
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Indian Inst Chem Technol, Fluoro & Agrochem Div, CSIR, Hyderabad 500007, India
Acad Sci & Innovat Res, Ghaziabad 201002, India Indian Inst Chem Technol, Fluoro & Agrochem Div, CSIR, Hyderabad 500007, India

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Anoop, Anakuthil
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Indian Inst Technol Kharagpur, Dept Chem, Kharagpur 721302, India Indian Inst Chem Technol, Fluoro & Agrochem Div, CSIR, Hyderabad 500007, India

Chandra, Rajesh
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Indian Inst Chem Technol, Fluoro & Agrochem Div, CSIR, Hyderabad 500007, India
Acad Sci & Innovat Res, Ghaziabad 201002, India Indian Inst Chem Technol, Fluoro & Agrochem Div, CSIR, Hyderabad 500007, India

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Karunakar, Galla V.
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Indian Inst Chem Technol, Fluoro & Agrochem Div, CSIR, Hyderabad 500007, India
Acad Sci & Innovat Res, Ghaziabad 201002, India Indian Inst Chem Technol, Fluoro & Agrochem Div, CSIR, Hyderabad 500007, India
机构:
[1] Indian Inst Chem Technol, Fluoro & Agrochem Div, CSIR, Hyderabad 500007, India
[2] Acad Sci & Innovat Res, Ghaziabad 201002, India
[3] Indian Inst Technol Kharagpur, Dept Chem, Kharagpur 721302, India
[4] Indian Inst Chem Technol, Ctr Xray Crystallog, CSIR, Hyderabad 500007, India
关键词:
C-H BONDS;
DIVERGENT SYNTHESIS;
INDOLES;
ALKYNES;
ACCESS;
D O I:
10.1021/acs.orglett.4c02770
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
The interaction of N-alkoxy-1H-indole-1-carboxamides with transition metals leads to indole-fused heterocyclic scaffolds through directing group leaving/migration, [3 + 2], N-C2 [4 + 1], and [4 + 2] annulations. However, the corresponding O-C2 [4 + 2] annulation reactions have never been reported. Herein, we report the chemoselective annulation of N-alkoxy-1H-indole-1-carboxamides catalyzed by Rh(III), affording [1,3]oxazinoindolones through a hitherto unknown reaction pathway. This unprecedented C2 oxygen cyclization, rather than the known C2 nitrogen cyclization to form oxazinoindolones via five key steps, has been explained using density functional theory.
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页码:8680 / 8685
页数:6
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Peking Univ, Coll Chem & Mol Engn, Minist Educ, Beijing Natl Lab Mol Sci, Beijing 100871, Peoples R China
Peking Univ, Coll Chem & Mol Engn, Minist Educ, Key Lab Bioorgan Chem & Mol Engn, Beijing 100871, Peoples R China
Peking Univ, Green Chem Ctr, Beijing 100871, Peoples R China Peking Univ, Coll Chem & Mol Engn, Minist Educ, Beijing Natl Lab Mol Sci, Beijing 100871, Peoples R China

Shi, Zhang-Jie
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Peking Univ, Coll Chem & Mol Engn, Minist Educ, Beijing Natl Lab Mol Sci, Beijing 100871, Peoples R China
Peking Univ, Coll Chem & Mol Engn, Minist Educ, Key Lab Bioorgan Chem & Mol Engn, Beijing 100871, Peoples R China
Peking Univ, Green Chem Ctr, Beijing 100871, Peoples R China
Chinese Acad Sci, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China
Nankai Univ, State Key Lab Elemental Organ Chem, Tianjin 300071, Peoples R China Peking Univ, Coll Chem & Mol Engn, Minist Educ, Beijing Natl Lab Mol Sci, Beijing 100871, Peoples R China
[40]
Rh(III)-Catalyzed C-H Activation/Cyclization of Indoles and Pyrroles: Divergent Synthesis of Heterocycles
[J].
Zhang, Yan
;
Zheng, Jing
;
Cui, Sunliang
.
JOURNAL OF ORGANIC CHEMISTRY,
2014, 79 (14)
:6490-6500

Zhang, Yan
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机构: Zhejiang Univ, Inst Mat Med, Hangzhou 310058, Zhejiang, Peoples R China

Zheng, Jing
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h-index: 0
机构: Zhejiang Univ, Inst Mat Med, Hangzhou 310058, Zhejiang, Peoples R China

Cui, Sunliang
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机构:
Zhejiang Univ, Inst Mat Med, Hangzhou 310058, Zhejiang, Peoples R China Zhejiang Univ, Inst Mat Med, Hangzhou 310058, Zhejiang, Peoples R China