𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A mild and stereospecific conversion of vicinal diols into olefins

✍ Scribed by Stephen Hanessian; Alberto Bargiotti; Marie LaRue

Book ID
108384562
Publisher
Elsevier Science
Year
1978
Tongue
French
Weight
222 KB
Volume
19
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

A mild procedure for the conversion of 1
A mild procedure for the conversion of 1,2-diols to olefins
✍ E.J. Corey; B. Hopkins πŸ“‚ Article πŸ“… 1982 πŸ› Elsevier Science 🌐 French βš– 238 KB

An improved procedure for the stereospecific synthesis of olefhm from 1,2-dials via the corresponding thionocarbonate is described. The introduction of the versatile oleflnic function by &oxygenation of a 1,2-diol is a useful technique in organic synthesis. Although numerous procedures have appeare

A mild conversion of vicinal diols to al
A mild conversion of vicinal diols to alkenes. Efficient transformation of ribonucleosides into 2β€²-ene and 2t',3β€²-dideoxynucleosides
✍ Morris J. Robins; Fritz Hansske; Nicholas H. Low; Ja In Park πŸ“‚ Article πŸ“… 1984 πŸ› Elsevier Science 🌐 French βš– 249 KB

a-Acetoxyisobutyryl bromide in "moist" acetonitrile converted adenosine to trans-3'(2')-bromo-2'(3')-acetates with <3% glycosyl cleavage. This mixture was acetylated, treated with Zn/Cu/DMF, and deacylated to give 81% of the 2'-alkene.