Original language | English |
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Pages (from-to) | 590-591 |
Number of pages | 2 |
Journal | Chemical Communications (London) |
Issue number | 12 |
DOIs | |
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 | Funder number |
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National Cancer Institute |