Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 Versatile pyrrole synthesis through ruthenium(II)-catalyzed alkene C-H bond functionalization on enamines.

Literature DB >> 23256885

Versatile pyrrole synthesis through ruthenium(II)-catalyzed alkene C-H bond functionalization on enamines.

Abstract

An efficient ruthenium(II) catalyst enabled broadly applicable oxidative alkyne annulations with electron-rich enamines to provide diversely decorated pyrroles, even in an aerobic fashion with air as the ideal oxidant.

Entities: Chemical

Mesh：

Substances：

Year: 2012 PMID： 23256885 DOI： 10.1021/ol303224e

Source DB: PubMed Journal: Org Lett ISSN： 1523-7052 Impact factor: 6.005

Keyword Cloud
Cited

7 in total

1. A mild and efficient AgSbF₆-catalyzed synthesis of fully substituted pyrroles through a sequential propargylation/amination/cycloisomerization reaction.

Authors: Satheesh Gujarathi; Xingui Liu; Lin Song; Howard Hendrickson; Guangrong Zheng
Journal: Tetrahedron Date: 2014-08-26 Impact factor: 2.457

2. Synthesis of unsymmetrically tetrasubstituted pyrroles and studies of AIEE in pyrrolo[1,2-a]pyrimidine derivatives.

Authors: Taian Li; Mong-Feng Chiou; Yajun Li; Changqing Ye; Min Su; Mengyu Xue; Xiaobin Yuan; Chuanchuan Wang; Wen-Ming Wan; Daliang Li; Hongli Bao
Journal: Chem Sci Date: 2022-04-20 Impact factor: 9.969

3. Catalytic 1,4-rhodium(III) migration enables 1,3-enynes to function as one-carbon oxidative annulation partners in C-H functionalizations.

Authors: David J Burns; Hon Wai Lam
Journal: Angew Chem Int Ed Engl Date: 2014-07-22 Impact factor: 15.336

Versatile pyrrole synthesis through ruthenium(II)-catalyzed alkene C-H bond functionalization on enamines.

1. A mild and efficient AgSbF₆-catalyzed synthesis of fully substituted pyrroles through a sequential propargylation/amination/cycloisomerization reaction.

2. Synthesis of unsymmetrically tetrasubstituted pyrroles and studies of AIEE in pyrrolo[1,2-a]pyrimidine derivatives.

3. Catalytic 1,4-rhodium(III) migration enables 1,3-enynes to function as one-carbon oxidative annulation partners in C-H functionalizations.

4. Direct Synthesis of Highly Substituted Pyrroles and Dihydropyrroles Using Linear Selective Hydroacylation Reactions.

Review 5. Progress and prospects in copper-catalyzed C-H functionalization.

6. Rh-catalyzed aerobic oxidative cyclization of anilines, alkynes, and CO.

7. Iodine-catalyzed diazo activation to access radical reactivity.

Versatile pyrrole synthesis through ruthenium(II)-catalyzed alkene C-H bond functionalization on enamines.

1. A mild and efficient AgSbF6-catalyzed synthesis of fully substituted pyrroles through a sequential propargylation/amination/cycloisomerization reaction.

2. Synthesis of unsymmetrically tetrasubstituted pyrroles and studies of AIEE in pyrrolo[1,2-a]pyrimidine derivatives.

3. Catalytic 1,4-rhodium(III) migration enables 1,3-enynes to function as one-carbon oxidative annulation partners in C-H functionalizations.

4. Direct Synthesis of Highly Substituted Pyrroles and Dihydropyrroles Using Linear Selective Hydroacylation Reactions.

Review 5. Progress and prospects in copper-catalyzed C-H functionalization.

6. Rh-catalyzed aerobic oxidative cyclization of anilines, alkynes, and CO.

7. Iodine-catalyzed diazo activation to access radical reactivity.

1. A mild and efficient AgSbF₆-catalyzed synthesis of fully substituted pyrroles through a sequential propargylation/amination/cycloisomerization reaction.