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Asymmetric hydroboration-oxidation of alkenes by means of deuterium or tritium labelled asymmetric monoalkylboranes

✍ Scribed by Alain Burgos; Jean-Marc Kamenka; Anne-Marie Moustier; Bernard Rousseau


Publisher
John Wiley and Sons
Year
1991
Tongue
French
Weight
229 KB
Volume
29
Category
Article
ISSN
0022-2135

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✦ Synopsis


Abstract

(2‐(1,3‐Dithianyl))myrtanylborane (MDBH~2~), a stable asymmetric monoalkylborane, was converted into deuterated or tritiated analogues used to prepare enantiomeric labelled alcohols from 1‐phenylcyclopentene with a high isotopic enrichment (90–95% for deuterium; 86–89% for tritium) and a high asymmetric induction (80% ee for deuterium; 75% ee for tritium).