𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of 1-3H-3, 3-dimethylallyl pyrophosphate

✍ Scribed by E. Cardemil; O. Cori


Publisher
John Wiley and Sons
Year
1973
Tongue
French
Weight
247 KB
Volume
9
Category
Article
ISSN
0022-2135

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

3, 3‐Dimethylallyl pyrophosphate (DMAPP) Labeled with ^3^H on C‐1 was prepared from the corresponding acid by esterification, reduction of the methyl ester with LiAl^3^H~4~ and pyrophosphorylation of the radioactive alcohol.

The products were purified by ion‐exchange chromatography, yielding a single radioactive compound. Phosphorus analysis and gas chromatography showed that the final product was DMAPP.


📜 SIMILAR VOLUMES


Improved preparation of 3-(1,1-dimethyla
✍ Xiangrui Jiang; Jianfeng Li; Rongxia Zhang; Hongli Guo; Shaolei Huang; Jingshan 📂 Article 📅 2009 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 63 KB

## Abstract magnified image An improved preparation method of 3‐(1,1‐dimethylallyl)decursinol from inexpensive commercially available start material was described. In the cyclization of **13**, silica gel was used as catalyst to give **1** with high purity and satisfying yield. J. Heterocyclic Che

ChemInform Abstract: Improved Preparatio
✍ Xiangrui Jiang; Jianfeng Li; Rongxia Zhang; Guo-Hongli Guo-Hongli; Shaolei Huang 📂 Article 📅 2009 🏛 John Wiley and Sons ⚖ 21 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

Synthesis of [3″-3H]taxol and [13-3H]tax
✍ George F. Taylor; Stephen S. Thornton; C. Ray Tallent; John A. Kepler 📂 Article 📅 1993 🏛 John Wiley and Sons 🌐 French ⚖ 677 KB

## Abstract 7‐Trietylsilylbaccatin III (11) was coupled with cis‐1‐benzoyl‐3‐triethylsiloxy‐4‐(3′‐bromophenyl)azetidin‐2‐one. Hydrolysis of the silyl groups gave 3″‐bromotaxol which was reduced with tritium gas to give[3″‐^3^H]taxol with specific activity of 19.3 Ci mmol. Reduction of 7‐triethylsil

Synthesis of 1-pyrenyloxirane-3,6,8-3H1
✍ Daniel J. McCaustland; Alexander B. Susàn; James C. Wiley Jr. 📂 Article 📅 1981 🏛 John Wiley and Sons 🌐 French ⚖ 225 KB

## Abstract The syntheses of 1‐pyrenyloxirane‐3,6,8‐^3^H~1~, **7**, and its precursor, pyrene‐1,3,6,8‐^3^H~1~, **4**, are described. The synthesis pathway includes a novel preparation of **4** from 1‐pyrenyllithium and tritiated water in theoretical yield.