ChemInform Abstract: Palladium-Catalyzed Tandem Cyclization-Anion Capture Processes. Part 3. Organoboron Anion Transfer Agents.

ChemInform ◽  
2010 ◽  
Vol 29 (1) ◽  
pp. no-no
Author(s):  
R. GRIGG ◽  
J. M. SANSANO ◽  
V. SANTHAKUMAR ◽  
V. SRIDHARAN ◽  
R. THANGAVELANTHUM ◽  
...  
Keyword(s):  
Palladium Catalyzed ◽  
Tandem Cyclization ◽  
Anion Transfer ◽  
Transfer Agents

ChemInform Abstract: Palladium Catalyzed Tandem Cyclization-Anion Capture Processes. Part 4. Organotin(IV) Transfer Agents.

ChemInform ◽  
2001 ◽  
Vol 32 (1) ◽  
pp. no-no
Author(s):  
Paul Fretwell ◽  
Ronald Grigg ◽  
Jose M. Sansano ◽  
Visuvanathar Sridharan ◽  
Sukanthini Sukirthalingam ◽  
...  
Keyword(s):  
Palladium Catalyzed ◽  
Tandem Cyclization ◽  
Transfer Agents

scholarly journals Palladium-Catalyzed Tandem Cyclization/Suzuki Coupling of 1,6-Enynes: Reaction Scope and Mechanism.

ChemInform ◽  
2005 ◽  
Vol 36 (31) ◽  
Author(s):  
Gangguo Zhu ◽  
Xiaofeng Tong ◽  
Jiang Cheng ◽  
Yanhui Sun ◽  
Dao Li ◽  
...  
Keyword(s):  
Suzuki Coupling ◽  
Palladium Catalyzed ◽  
Tandem Cyclization

Tandem cyclization of o-alkynylanilines with isocyanides triggered by intramolecular nucleopalladation: access to heterocyclic fused 2-aminoquinolines

2018 ◽  
Vol 54 (50) ◽  
pp. 6855-6858 ◽  
Author(s):  
Wanqing Wu ◽  
Meng Li ◽  
Jia Zheng ◽  
Weigao Hu ◽  
Chunsheng Li ◽  
...  
Keyword(s):  
Palladium Catalyzed ◽  
Tandem Cyclization ◽  
Novel Strategy

A novel strategy for the synthesis of heterocyclic fused 2-aminoquinolines via palladium-catalyzed tandem cyclization of o-alkynylanilines and isocyanides has been developed.

Palladium-catalyzed tandem cyclization/sulfonylation of homoallenyl amides with sodium sulfinates

2017 ◽  
Vol 15 (34) ◽  
pp. 7204-7211 ◽  
Author(s):  
Yimei Wan ◽  
Jian Zhang ◽  
Yongtao Chen ◽  
Lichun Kong ◽  
Fang Luo ◽  
...  
Keyword(s):  
Palladium Catalyzed ◽  
Tandem Cyclization

A palladium-catalyzed cyclizative sulfonylation of homoallenyl amides has been developed using sodium sulfinates as the sulfonylation reagent and PhI(O2CCF3)2 as the oxidant, providing a facile access to 2-amino-5-sulfonylmethylfurans in good to excellent yields.

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