𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Microwave-assisted expeditious synthesis of 5-fluoroalkyl-3-(aryl/alkyl)-oxazolidin-2-ones

✍ Scribed by Yang, Bo; Shi, Luyan; Wu, JingJing; Fang, Xiang; Yang, Xueyan; Wu, Fanhong

Book ID
120008873
Publisher
Elsevier Science
Year
2013
Tongue
French
Weight
346 KB
Volume
69
Category
Article
ISSN
0040-4020

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Regio- and stereoselective microwave-ass
Regio- and stereoselective microwave-assisted synthesis of 5-alkyl-4-alkenyl-4-phenyl-1,3-oxazolidin-2-ones
✍ Marta Amador; Xavier Ariza; JΓ©rΓ©mie Boyer; Lucia D’Andrea; Jordi Garcia; Jaume G πŸ“‚ Article πŸ“… 2010 πŸ› Elsevier Science 🌐 French βš– 588 KB

Quaternary a-amino acids a b s t r a c t Chiral symmetrical alk-2-yne-1,4-diols have been stereoselectively transformed into 5-alkyl-4-alkenyl-4phenyl-1,3-oxazolidin-2-ones, which are precursors of quaternary a-amino b-hydroxy acids. The key step was the cyclization of the bis(tosylcarbamates) of 2-

Solid phase synthesis of 3,5-disubstitut
Solid phase synthesis of 3,5-disubstituted oxazolidin-2-ones
✍ S.K. Rastogi; G.K. Srivastava; S.K. Singh; R.K. Grover; R. Roy; B. Kundu πŸ“‚ Article πŸ“… 2002 πŸ› Elsevier Science 🌐 French βš– 140 KB

A versatile method for the solid phase synthesis of oxazolidin-2-ones is described. A resin bound phenolic group was treated with (Β±)-epichlorohydrin followed by opening of the epoxide ring with sodium azide. The resulting 1-azido-3-aryloxypropan-2-ol was treated with p-nitrophenylchloroformate and