𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A New, Stereospecific Olefin Synthesis from 1,2-Diols

✍ Scribed by Corey, E. J.; Winter, Roland A. E.


Book ID
121076788
Publisher
American Chemical Society
Year
1963
Tongue
English
Weight
283 KB
Volume
85
Category
Article
ISSN
0002-7863

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Stereospecific deoxygenation of 1,2-diol
✍ John L. King; Bruce A. Posner; Kwok Tim Mak; Nien-chu C. Yang πŸ“‚ Article πŸ“… 1987 πŸ› Elsevier Science 🌐 French βš– 203 KB

The 2-dimethylamino-1,3-dioxolane derivatives of 1,2-diols when treated with trifluoromethane sulfonic anhydride and diisopropylethylamine in toluene give the corresponding olefins stereospecifically under mild experimental conditions. Many methods are known for the conversion of 1,2-diols into the

Total synthesis of (+)-spatol. A stereos
✍ Robert G. Salomon; Basudeb Basu; Subhas Roy; Ram B. Sharma πŸ“‚ Article πŸ“… 1989 πŸ› Elsevier Science 🌐 French βš– 242 KB

A total synthesis of (+)-spat01 (1) was achieved which depends upon a novel stereospecific transformation of trans-2,3-epoxy-1,4-diols to generate the sensitive allylic vicinal cisdiepoxide in 1. Spat01 (l), a structurally and functionally complex minor metabolite produced by a tropical

Synthesis of diols from 1,2-epoxy-3-bute
✍ L. V. Mel’nik; S. S. Srednev; G. V. Rybina; A. E. Meshechkina; A. S. Shevchuk; A πŸ“‚ Article πŸ“… 2007 πŸ› Springer 🌐 English βš– 150 KB