Diastereoselective Synthesis of Substituted Tetrahydrofurans via Prins Cyclization of Enol Ethers

2014 ◽  
Vol 79 (18) ◽  
pp. 8592-8598 ◽  
Author(s):  
Paramartha Gogoi ◽  
Vijay K. Das ◽  
Anil K. Saikia
2014 ◽  
Vol 12 (36) ◽  
pp. 7026-7035 ◽  
Author(s):  
Anil K. Saikia ◽  
Kiran Indukuri ◽  
Jagadish Das

A diastereoselective synthesis of 4-O-tosyl piperidine containing azabicyclic derivatives has been established via Prins cyclization reaction. This protocol has been applied for the total synthesis of (±)-epi-indolizidine 167B and 209D.


2012 ◽  
Vol 58 ◽  
pp. 1-11 ◽  
Author(s):  
Saulo L. Capim ◽  
Paulo H.P. Carneiro ◽  
Paloma C. Castro ◽  
Maithê R.M. Barros ◽  
Bruno G. Marinho ◽  
...  

Synthesis ◽  
2011 ◽  
Vol 2012 (02) ◽  
pp. 297-303 ◽  
Author(s):  
Basi Reddy ◽  
Dudhmal Chaya ◽  
Jhillu Yadav ◽  
René Grée

SynOpen ◽  
2019 ◽  
Vol 03 (01) ◽  
pp. 36-45
Author(s):  
Sujit Sarkar ◽  
Namita Devi ◽  
Bikoshita Porashar ◽  
Santu Ruidas ◽  
Anil Saikia

Intramolecular cyclization of enol ethers mediated by para-toluenesulfonic acid leads to substituted tetrahydropyrans in good to moderate yields. The reaction is diastereoselective.


Synthesis ◽  
2008 ◽  
Vol 2008 (3) ◽  
pp. 395-400 ◽  
Author(s):  
Jhillu Yadav ◽  
Basi Subba Reddy ◽  
Gunda Narayana Kumar ◽  
Seema Aravind

Sign in / Sign up

Export Citation Format

Share Document