Synthesis of tritiated diborane and cryptand [2.2.2]
β Scribed by Kayhan Garmestani; Jeanne M. Link; Kenneth A. Krohn
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- French
- Weight
- 327 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
In order to provide a method for in vivo and in vitro detection of cryptand [2.2.2], tritiated cryptand was synthesized by reduction of appropriate bicyclic diamide with tritiated diborane. As part of this synthesis, tritiated diborane was synthesized by the reaction of tritiated sodium borohydride with boron trifluoride etherate and trapped in dry THF. This is a potentially useful agent for selective tritiation of molecules with functional groups which are prone to electrophilic attack.
π SIMILAR VOLUMES
Tritiated poly-L-lysine (y,&T\*) (IX) waa prepared according to the following procedure: Tritiated DL-lysine (y,&T\*) (111) was derived from acetarnino-(4amino-A\*-buteny1)-diethylmalonate (I) by tritiation followed by acid hydrolysis. The racemic tritiated lysine was converted to its e,N-trifluoroa
## Abstract The synthesis of 4,6β^2^H~2~β1,2,3βbenzenetriol from 1,2,3βbenzenetriol was possible under both acid and base catalyzed conditions. However, under simulated physiological conditions it was observed that the label underwent exchange and was lost. Using a three step synthesis, 5β^2^Hβ1,2,
## Abstract The synthesis of polyunsaturated trialkyl glyceryl ether tritiated at Cβ2 of the glycerol carbon chain having identical 1,3βalkyl groups is described.