Diastereoselective Synthesis ofsyn-1,3-Diols by Titanium-Mediated Reductive Coupling of Propargylic Alcohols

2010 ◽  
Vol 12 (2) ◽  
pp. 288-290 ◽  
Author(s):  
Guo-Qiang Tian ◽  
Thomas Kaiser ◽  
Jiong Yang
Keyword(s):  
Reductive Coupling ◽  
Diastereoselective Synthesis ◽  
Propargylic Alcohols

Diastereoselective synthesis of 1,2-diphenyl-1,2-diaminoethanes by Yb(OTf)3 accelerated reductive coupling of imines

1998 ◽  
Vol 39 (20) ◽  
pp. 3333-3336 ◽  
Author(s):  
Rita Annunziata ◽  
Maurizio Benaglia ◽  
Mauro Cinquini ◽  
Franco Cozzi ◽  
Laura Raimondi
Keyword(s):  
Reductive Coupling ◽  
Diastereoselective Synthesis

ChemInform Abstract: Diastereoselective Synthesis of 1,2-Diphenyl-1,2-diaminoethanes by Yb(OTf)3 Accelerated Reductive Coupling of Imines.

ChemInform ◽  
2010 ◽  
Vol 29 (33) ◽  
pp. no-no
Author(s):  
R. ANNUNZIATA ◽  
M. BENAGLIA ◽  
M. CINQUINI ◽  
F. COZZI ◽  
L. RAIMONDI
Keyword(s):  
Reductive Coupling ◽  
Diastereoselective Synthesis

Indium(iii) chloride catalyzed highly diastereoselective domino synthesis of indenodithiepines and indenodithiocines

2015 ◽  
Vol 51 (4) ◽  
pp. 707-710 ◽  
Author(s):  
Sengodagounder Muthusamy ◽  
Manickasamy Sivaguru ◽  
Eringathodi Suresh
Keyword(s):  
Domino Reaction ◽  
Diastereoselective Synthesis ◽  
Propargylic Alcohols

An atom-economical diastereoselective synthesis of indenodithiepines and indenodithiocines has been developed via a domino reaction of propargylic alcohols and dithioacetals in the presence of InCl3 as a catalyst.

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