Modeling the Chemical Conversion of Organic Compounds in Sodium Borohydride Reduction Reactions

2008 ◽  
Vol 12 (3) ◽  
pp. 456-463 ◽  
Author(s):  
Ruth M. Tinnacher ◽  
Bruce D. Honeyman

1974 ◽  
Vol 52 (3) ◽  
pp. 376-380 ◽  
Author(s):  
Roger N. Renaud

Electrochemical reduction of 1-chloro-, 1-bromo-, 1-iodo-, 1-chloro-4-methyl-, and 1-bromo-4-methyl naphthalene was done in presence of deuterated water. The deuterium content of the naphthalene obtained reveals that the mechanism for the bromo and the iodo derivatives might involve either a simultaneous transfer of two electrons or an organometallic intermediate, while reduction of the chloro derivative might proceed at least partially via a radical intermediate.The synthesis of 1-chloro-4-methylnaphthalene from 1-chloro-4-chloromethylnaphthalene was achieved either by selective sodium borohydride reduction or by selective electrochemical reduction.





1965 ◽  
Vol 30 (7) ◽  
pp. 2241-2246 ◽  
Author(s):  
Harold Zinnes ◽  
Roger A. Comes ◽  
Francis R. Zuleski ◽  
Albert N. Caro ◽  
John Shavel


ChemInform ◽  
2010 ◽  
Vol 31 (36) ◽  
pp. no-no
Author(s):  
Francesco Fringuelli ◽  
Ferdinando Pizzo ◽  
Luigi Vaccaro


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