## Abstract Synthesis of furosemide. specifically labelled at the 2‐furanylmethyl α‐position with ^2^H or ^3^H is reported. This synthesis required reduction of N‐[(2‐furanyhethyl)amino]‐4‐chloro‐5‐(N‐acetylaminosulfonyl)benzoia acid (2) with sodium ^2^H‐ or ^3^H‐borohydride. followed by alkaline h
Synthesis of the epimeric 2-bromocholesterols and their conversion into (2α-3H)cholesterol and [2ß-3H]cholesterol
✍ Scribed by J. Römer; H. Wagner; K. Ponsold
- Publisher
- John Wiley and Sons
- Year
- 1984
- Tongue
- French
- Weight
- 398 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
The s y n t h e s i s of t h e epirceric 2-bromocbolesterols is d e s c r i b e d . T h e i r r e d u c t i v e c a t a l y z e d debromination w i t h T2 a f f o r d s c20<-'HJa.nd [2B -311]cbolesterol r e s p e c t i v e l y . The [Z -3E]cholesterols c a n be s y n t h e s i s e d w i t h a r a d i o c h e m i c a l pul'ity >98% aiid s p e c i f i c e c t i v i t i e s of about 600 -700 GSq/mmol. The l a b e l l i n g r e a c t i o n s proceed under r e t e n t i o n .
📜 SIMILAR VOLUMES
## Abstract The synthesis of [2‐^3^H~2~]‐2‐aminoethanesulfonate [2‐^3^H]‐taurine by the reduction of cyanomethanesulfonic acid with tritium gas is described. The conversion of [2‐^3^H]‐taurine and its ^14^C and ^35^S isotopic forms to 2‐aminoethanesulfinate (hypotaurine) was accomplished by convert
Two new nickel metavanadate hydrates, Ni(VO 3 ) 2 ' 4H 2 O and -Ni(VO 3 ) 2 ' 2H 2 O, have been synthesized using a 99chimie douce:: process; their crystal structures have been solved from single-crystal X-ray di4raction data. The tetrahydrate Ni(VO 3 ) 2 ' 4H 2 O crystallizes in the monoclinic spac
## Abstract Tropinone was reduced using sodium borodeuteride to give a mixture of the epimers [3‐^2^H] tropine and [3‐^2^H]pseudotropine with the latter compound predominating and constituting about 70% of the mixture. Crystallisation of the product from diethyl ether gave crystals of pure [3‐^2^H]
## Abstract magnified image A series of substituted 5‐, 6‐, 7‐, and 8‐hydroxy‐3‐phenyl‐2__H__‐1,3‐benzoxazine‐2,4(3__H__)‐diones (**5–8**) was synthesized by cyclization of corresponding dihydroxy‐__N__‐phenylbenzamides (**1–4**) with methyl chloroformate. The starting compounds **1–4** were prepa