Reaction of trialkylboranes with sodium diethyldihydroaluminate in the presence of 1,4-diazabicyclo[2.2.2]octane. a convenient, general method for preparation of sodium trialkylborohydrides-Reference-Cited by-同舟云学术

Reaction of trialkylboranes with sodium diethyldihydroaluminate in the presence of 1,4-diazabicyclo[2.2.2]octane. a convenient, general method for preparation of sodium trialkylborohydrides

Published:1993-01 Issue:37 Volume:49 Page:8311-8316
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Hubbard John L.,Fuller Joseph C.,Jackson Thomas C.,Singaram Bakthan

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference18 articles.

1. Forty years of hydride reductions

2. NB-Enantride, a new chiral trialkylborohydride for the asymmetric reduction of ketones

3. Hydride-induced carbonylation of organoboranes. Evidence that all complex metal hydrides evaluated react by way of alkali metal trialkylborohydride intermediates

4. Structure and derivatization of the product from carbonylation of lithium triethylborohydride

5. Formation and instability of an α-acetoxyborane

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