A new synthesis of amines with diborane

Alfred Hassner, P. Catsoulacos

Research output: Contribution to journalArticlepeer-review

18 Scopus citations
Original languageEnglish
Pages (from-to)590-591
Number of pages2
JournalChemical Communications (London)
Issue number12
DOIs
StatePublished - 1967
Externally publishedYes

Bibliographical note

Funding Information:
substantiated by the analogous behaviour of The fact that oximes are reduced by diborane to oxime tosylates (see Table). $ hydroxylamines while oxime acetates yield amine This investigation was supported in part by a can be explained by co-ordination of borane with U.S. Public Health Service Research Grant from one of the acetate oxygens, thus providing a good the National Cancer Institute. leaving group that facilitates internal hydride transfer. This is consistent with the fact that (Received, May lst, 1967; Corn.

Funding

substantiated by the analogous behaviour of The fact that oximes are reduced by diborane to oxime tosylates (see Table). $ hydroxylamines while oxime acetates yield amine This investigation was supported in part by a can be explained by co-ordination of borane with U.S. Public Health Service Research Grant from one of the acetate oxygens, thus providing a good the National Cancer Institute. leaving group that facilitates internal hydride transfer. This is consistent with the fact that (Received, May lst, 1967; Corn.

FundersFunder number
National Cancer Institute

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