REGIOSELECTIVE AND STEREOSELECTIVE TRITIATION OF THE JUVENOID ANALOG W-328

Authors
ELBERT T CERNY B WIMMER Z SERGENT L
Citation
T. Elbert et al., REGIOSELECTIVE AND STEREOSELECTIVE TRITIATION OF THE JUVENOID ANALOG W-328, Collection of Czechoslovak Chemical Communications, 58(5), 1993, pp. 1164-1168
Citations number
7
Categorie Soggetti
Chemistry
Journal title
Collection of Czechoslovak Chemical Communications → ACNP
ISSN journal
00100765
Volume
58
Issue
5
Year of publication
1993
Pages
1164 - 1168
Database
ISI
SICI code
0010-0765(1993)58:5<1164:RASTOT>2.0.ZU;2-U
Abstract
The juvenoid analog (2-(ethoxycarbamato)ethoxy)benzyl)-1-cyclohexanone ethylene acetal (I) (W 328) was labelled by H-3 in the benzyl positio n by the CESG method. H-3 NMR revealed the stereoselectivity of the la belling. The results are compared with the data published in the liter ature and discussed in the terms of stereoelectronic requirements.