𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Improved preparation of (±)-(1,3/2,4)-5-cyclohexene-1,2,3,4-tetrol [(±)-conduritol-B] and its reaction with hydrobromic and hydrochloric acid; synthesis and characterisation of some (±)-1-deoxy-1-halo- and (±)-1,4-dideoxy-1,4-dihaloconduritols

✍ Scribed by Zhao-Xia Guo; Alan H. Haines; Simon M. Pyke; Susan G. Pyke; Richard J.K. Taylor


Publisher
Elsevier Science
Year
1994
Tongue
English
Weight
530 KB
Volume
264
Category
Article
ISSN
0008-6215

No coin nor oath required. For personal study only.

✦ Synopsis


The configurations of 1 and 2 were tentatively assigned [2] on the relative rates of dehydrobromination with sodium ethoxide and on the conversion [l] of one of them into a previously described [ 31 triacetate.


📜 SIMILAR VOLUMES


Total Syntheses of (−)-Conduritol B ((−)
✍ Claude Le Drian; Jean-Paul Vionnet; Pierre Vogel 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 German ⚖ 585 KB

## Abstract The ‘naked sugar’ (+)‐(1__R__,2__R__4__R__)‐2‐__endo__‐cyano‐7‐oxabicyclo[2.2.1]hept‐5‐sn‐2‐__exo__‐yl acetate ((+)‐4) was converted (7 steps, 45% overall) with high stereoselectivity into (−)‐(4__R__,5__S__,6__R__)‐4,5,6‐tris{[(__tert__‐butyl)dimethylsilyl]oxy}cyclohex‐2‐en‐1‐one ((−)‐

ChemInform Abstract: Reactions with Hydr
✍ Abdou O. Abdelhamid; Zeineb H. Ismail; Anhar Abdel-Aziem 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 38 KB 👁 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

1,2,4-Triazoles. Improved synthesis of 5
✍ Francesco Paolo Invidiata; Giancarlo Furná; Ilaria Lampronti; Daniele Simoni 📂 Article 📅 1997 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 243 KB

## Abstract The reaction of thiocarbohydrazide with carboxylic acids at the melting temperature allows an improved preparation of the S‐substituted 4‐amino‐3‐mercapto‐1,2,4‐triazole heterocycles. The crude 4‐amino‐5‐mercapto‐1,2,4‐triazoles react easily with carboxylic acids or carboxylic acid chlo