A new synthesis of amines with diborane

Alfred Hassner; P. Catsoulacos

doi:10.1039/C19670000590

A new synthesis of amines with diborane

Alfred Hassner
, P. Catsoulacos

University of Colorado Boulder

Research output: Contribution to journal › Article › peer-review

18 Scopus citations

Original language	English
Pages (from-to)	590-591
Number of pages	2
Journal	Chemical Communications (London)
Issue number	12
DOIs	https://doi.org/10.1039/C19670000590
State	Published - 1967
Externally published	Yes

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.

Funders
National Cancer Institute

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10.1039/C19670000590

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title = "A new synthesis of amines with diborane",

author = "Alfred Hassner and P. Catsoulacos",

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. ",

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PY - 1967

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A new synthesis of amines with diborane

Bibliographical note

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