ChemInform Abstract: Palladium-Catalyzed Tandem Allenyl and Aryl C-N Bond Formation: Efficient Access to N-Functionalized Multisubstituted Indoles.

ChemInform ◽  
2012 ◽  
Vol 43 (52) ◽  
pp. no-no
Author(s):  
Bingxin Liu ◽  
Xiaohu Hong ◽  
Dong Yan ◽  
Shuguang Xu ◽  
Xiaomei Huang ◽  
...  
Keyword(s):  
Bond Formation ◽  
Efficient Access ◽  
Palladium Catalyzed

Palladium-Catalyzed Tandem Allenyl and Aryl C–N Bond Formation: Efficient Access toN-Functionalized Multisubstituted Indoles

2012 ◽  
Vol 14 (17) ◽  
pp. 4398-4401 ◽  
Author(s):  
Bingxin Liu ◽  
Xiaohu Hong ◽  
Dong Yan ◽  
Shuguang Xu ◽  
Xiaomei Huang ◽  
...  
Keyword(s):  
Bond Formation ◽  
Efficient Access ◽  
Palladium Catalyzed

ChemInform Abstract: Efficient Access to 1,4-Benzothiazine: Palladium-Catalyzed Double C-S Bond Formation Using Na2S2O3as Sulfurating Reagent.

ChemInform ◽  
2013 ◽  
Vol 44 (40) ◽  
pp. no-no
Author(s):  
Zongjun Qiao ◽  
Hui Liu ◽  
Xiao Xiao ◽  
Yana Fu ◽  
Jianpeng Wei ◽  
...  
Keyword(s):  
Bond Formation ◽  
Efficient Access ◽  
Palladium Catalyzed

Efficient Access to 1,4-Benzothiazine: Palladium-Catalyzed Double C–S Bond Formation Using Na2S2O3 as Sulfurating Reagent

2013 ◽  
Vol 15 (11) ◽  
pp. 2594-2597 ◽  
Author(s):  
Zongjun Qiao ◽  
Hui Liu ◽  
Xiao Xiao ◽  
Yana Fu ◽  
Jianpeng Wei ◽  
...  
Keyword(s):  
Bond Formation ◽  
Efficient Access ◽  
Palladium Catalyzed

Sequential C-Selective Difluoromethylation/Pd-Catalyzed Decarboxylative Protonation: An Efficient Access to Tertiary Difluoromethylated Scaffolds

2019 ◽  
Author(s):  
Nicolas Duchemin ◽  
Roberto Buccafusca ◽  
Marc Daumas ◽  
Vincent Ferey ◽  
Stellios Arseniyadis
Keyword(s):  
Drug Development ◽  
Late Stage ◽  
Efficient Access ◽  
Palladium Catalyzed ◽  
General Method

We report here a general method that allows a highly straightforward access to tertiary difluoromethylated compounds. The strategy relies on a two-step sequence featuring a C-selective electrophilic difluoromethylation and an unprecedented palladium-catalyzed decarboxylative protonation. Considering the generality of the method and the attractive properties offered by the difluoromethyl group, this approach provides a valuable tool for late-stage functionalization and drug development.<br>

Palladium-catalyzed cascade cyclizations involving C–C and C–X bond formation: strategic applications in natural product synthesis

2021 ◽  
Author(s):  
K. R. Holman ◽  
A. M. Stanko ◽  
S. E. Reisman
Keyword(s):  
Natural Product ◽  
Bond Formation ◽  
Natural Product Synthesis ◽  
Cascade Cyclizations ◽  
Palladium Catalyzed ◽  
Multiple Rings

This tutorial review highlights the use of palladium-catalyzed cascade cyclizations in natural product synthesis, focusing on cascades that construct multiple rings and form both C–C and C–X (X = O, N) bonds in a single synthetic operation.

A Valuable Synthesis of Pyrrolo[1,2-a]quinoxalines, Indolo[1,2-a]quinoxalines and their Aza-Analogues by Palladium-Catalyzed Intramolecular Carbon-Nitrogen Bond Formation

Synthesis ◽  
2005 ◽  
Vol 2005 (17) ◽  
pp. 2881-2886 ◽  
Author(s):  
Egle M. Beccalli ◽  
Giorgio Abbiati ◽  
Gianluigi Broggini ◽  
Giuseppe Paladino ◽  
Elisabetta Rossi
Keyword(s):  
Bond Formation ◽  
Palladium Catalyzed ◽  
Nitrogen Bond
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