| 21. |
Hydrogen bonding in organic synthesis. Part 9. The sulphenylation of fluoride-activated β-dicarbonyls |
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Canadian Journal of Chemistry,
Volume 56,
Issue 1,
1978,
Page 141-143
James H. Clark,
Jack M. Miller,
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摘要:
Various α-arylthio-β-dicarbonyls have been prepared by the room temperature reaction of β-dicarbonyltetraethylammonium fluoride monosolvates with aryl disulphides. The disulphides are formed by thein situfluoride-assisted air oxidation of aryl thiols.
ISSN:0008-4042
DOI:10.1139/v78-021
出版商:NRC Research Press
年代:1978
数据来源: NRC
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| 22. |
Syntheses related to the octodiose in apramycin. Part II |
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Canadian Journal of Chemistry,
Volume 56,
Issue 1,
1978,
Page 144-146
Harold C. Jarrell,
Walter A. Szarek,
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PDF (127KB)
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摘要:
Derivatives of two octodioses have been synthesized from methyl α-D-glucopyranoside and have been shown to possess atrans-decalin structure. The new octodiose derivatives may be useful in the synthesis of aminooctodioses which occur in apramycin and oxyapramycin.
ISSN:0008-4042
DOI:10.1139/v78-022
出版商:NRC Research Press
年代:1978
数据来源: NRC
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