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Synthesis 2005(8): 1279-1290
DOI: 10.1055/s-2005-861878
DOI: 10.1055/s-2005-861878
PAPER
© Georg Thieme Verlag Stuttgart · New York
The Synthesis and Reactivity of Phosphinous Acid-Boranes
Further Information
Received
3 January 2005
Publication Date:
17 March 2005 (online)
Publication History
Publication Date:
17 March 2005 (online)
Abstract
Phosphinic acid chlorides are converted directly into phosphinous acid-boranes in a process utilizing BH3·THF complex as a reducing agent. The process is general and affords phosphinous acid-boranes in good to very high yields. Phosphinous acid-boranes have been found to react readily with alkylating, acylating, reducing, halogenating and deborating agents to produce the corresponding phosphinous acid-borane esters, phosphinous acid-borane anhydrides, sec-phosphine oxides, sec-phosphine boranes and phosphinic acid halides, respectively. The efficient procedures for these conversions have been developed and their scope has been outlined.
Key words
phosphorus - boron - alkylation - acylation - halogenation
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