Stereoselective synthesis of organosulfur compounds incorporating N-aromatic heterocyclic motifs and quaternary carbon centers via a sulfa-Michael triggered tandem reaction

2015 ◽  
Vol 51 (47) ◽  
pp. 9714-9717 ◽  
Author(s):  
Tianyou Qin ◽  
Lu Cheng ◽  
Sean Xiao-An Zhang ◽  
Weiwei Liao
Keyword(s):  
Michael Addition ◽  
Stereoselective Synthesis ◽  
Tandem Reaction ◽  
Organosulfur Compounds ◽  
The Novel ◽  
Quaternary Carbon ◽  
Carbon Centers ◽  
Aromatic Heterocyclic

The novel sulfa-Michael addition (SMA)-triggered tandem reaction was developed by combining a SMA reaction with a simultaneous rearomatization process.

A rhodium-catalyzed tandem reaction of N-sulfonyl triazoles with indoles: access to indole-substituted indanones

2017 ◽  
Vol 53 (65) ◽  
pp. 9089-9092 ◽  
Author(s):  
Hao Yuan ◽  
Jianxian Gong ◽  
Zhen Yang
Keyword(s):  
Tandem Reaction ◽  
Quaternary Carbon ◽  
Carbon Centers

Rhodium(ii)-catalyzed tandem reaction of N-sulfonyl triazoles with indoles delivered structurally diverse indole-substituted indanones bearing vicinal quaternary carbon centers.

ChemInform Abstract: Acid-Promoted Rearrangement of Cyclic α,β-Epoxy Acylates: Stereoselective Synthesis of Spirocyclanes and Quaternary Carbon Centers.

ChemInform ◽  
2010 ◽  
Vol 28 (52) ◽  
pp. no-no
Author(s):  
Y. KITA ◽  
S. KITAGAKI ◽  
Y. YOSHIDA ◽  
S. MIHARA ◽  
D.-F. FANG ◽  
...  
Keyword(s):  
Stereoselective Synthesis ◽  
Quaternary Carbon ◽  
Carbon Centers

Acid-Promoted Rearrangement of Cyclic α,β-Epoxy Acylates:  Stereoselective Synthesis of Spirocyclanes and Quaternary Carbon Centers

1997 ◽  
Vol 62 (15) ◽  
pp. 4991-4997 ◽  
Author(s):  
Yasuyuki Kita ◽  
Shinji Kitagaki ◽  
Yutaka Yoshida ◽  
Sachiko Mihara ◽  
Dai-Fei Fang ◽  
...  
Keyword(s):  
Stereoselective Synthesis ◽  
Quaternary Carbon ◽  
Carbon Centers
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