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Reductive Dehalogenation of Organic Compounds by Sodium Telluride

✍ Scribed by Dr. W. Mack


Publisher
John Wiley and Sons
Year
1967
Tongue
English
Weight
222 KB
Volume
6
Category
Article
ISSN
0044-8249

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✦ Synopsis


a ; M c H o '0 sible to obtain aphenyl boron-azomethine chelate [B(C6H5)2+] in which with tetraphenyldiboron oxide only one [cf. (4)] (m.p. 130-135 'C, yellow) but with BF3 both chelating groups react (m.p. 276-277 "C, yellow, fluorescene blue green).


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## Abstract Reduction is a fundamental transformation in organic synthesis. Since its discovery by Brown and co‐workers, sodium borohydride is the most frequently hydride used in reduction processes. Owing to the importance of this reagent in modern organic synthesis, the aim of this review is to h