Stereoselective synthesis of [3.3.0] fused lactones (γ-butyrolactones) of sugars and nucleosides by free radical intramolecular cyclization

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Sonsoles Velázquez ◽  
Sophie Huss ◽  
María-José Camarasa
1996 ◽  
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Mario D. Bachi ◽  
Nira Bar-Ner ◽  
Artem Melman

2020 ◽  
Vol 9 (7) ◽  
pp. 1040-1044 ◽  
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Ya‐Nan Wu ◽  
Tian‐Shu Zhang ◽  
Wen‐Juan Hao ◽  
Shu‐Jiang Tu ◽  
Bo Jiang

Tetrahedron ◽  
2005 ◽  
Vol 61 (11) ◽  
pp. 2767-2778 ◽  
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Pedro Almendros ◽  
Alberto Rodríguez-Vicente ◽  
M. Pilar Ruiz

2002 ◽  
Vol 31 (2) ◽  
pp. 148-149 ◽  
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Hitomi Kadohama ◽  
Tadashi Nakata

1993 ◽  
Vol 29 (8) ◽  
pp. 857-877
Author(s):  
S. S. Zlot-skii ◽  
M. V. Kochinashvili ◽  
D. L. Rakhmankulov

2003 ◽  
Vol 68 (26) ◽  
pp. 10087-10091 ◽  
Author(s):  
Verónica I. Dodero ◽  
Liliana C. Koll ◽  
M. Belén Faraoni ◽  
Terence N. Mitchell ◽  
Julio C. Podestá

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.


ChemInform ◽  
2010 ◽  
Vol 25 (20) ◽  
pp. no-no
Author(s):  
S. S. ZLOTSKII ◽  
M. V. KOCHINASHVILI ◽  
D. L. RAKHMANKULOV

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