𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A novel stereoselective synthesis of 1,2,3-trisubstituted cyclopentanes

✍ Scribed by T. Akiyama; T. Fujii; H. Ishiwari; T. Imagawa; M. Kawanisi

Publisher
Elsevier Science
Year
1978
Tongue
French
Weight
123 KB
Volume
19
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Stereoselective synthesis of 2,3,4-trisu
Stereoselective synthesis of 2,3,4-trisubstituted tetrahydrofurans
✍ Steven R. Angle; Daniel S. Bernier; Keith Chann; Darin E. Jones; Musong Kim; Mar πŸ“‚ Article πŸ“… 1998 πŸ› Elsevier Science 🌐 French βš– 190 KB

The stereoselective synthesis of trisubstituted tetrahydrofurans from benzyl diazoacetate and cΒ’-alkyl-~-benzyloxyaldehydes or cΒ’-alkyl-~-(triethylsilyl)oxyaldehydes is described.

Stereospecific synthesis of t,t-1,2,3-tr
Stereospecific synthesis of t,t-1,2,3-trisubstituted cyclopentanes and of angularly disubstituted t-hydrindanols
✍ Takeshi Imagawa; Syuichi Sugita; Tetsuo Akiyama; Mituyosi Kawanisi πŸ“‚ Article πŸ“… 1981 πŸ› Elsevier Science 🌐 French βš– 607 KB

Anodic oxidative decarboxylation of endo-3-methoxycarbonyl-7-oxabicyclo[2.2.llheptane-endo-2-carboxylate anion gave exclusively an oxygenassisted Wagner-Meerwein-rearranged product, methyl 3-methoxy-2-oxabicyclo[2.2.1]heptane-anti-7-carboxylate, constituting a method for the stereospecific synthesis