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1. |
Ionic Reactions of Sulfonic Acid Esters |
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Sulfur reports,
Volume 19,
Issue 1,
1996,
Page 1-59
RichardFrancis Langler,
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PDF (1709KB)
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摘要:
This review covers recent progress (since the late 1980's) in the solution phase reactions of sulfonic acid esters. Some discussion of reactions which have yet to be explored experimentally is also provided.
ISSN:0196-1772
DOI:10.1080/01961779608047904
出版商:Taylor & Francis Group
年代:1996
数据来源: Taylor
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2. |
The Thiocarbonyl Group in Carbohydrate Chemistry |
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Sulfur reports,
Volume 19,
Issue 1,
1996,
Page 61-159
JoséManuel García Fernandez,
CarmenOrtiz Mellet,
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PDF (3458KB)
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摘要:
Recent developments in the chemistry of thiocarbonyl carbohydrate derivatives are reviewed in this article. Emphasis has been placed on the interactions between the various functional groups that may coexist in a given molecule as well as the synthetic, biological, and technical applications of this family of compounds.
ISSN:0196-1772
DOI:10.1080/01961779608047905
出版商:Taylor & Francis Group
年代:1996
数据来源: Taylor
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3. |
The Reactions of Sulfides and Sulfenic Acid Derivatives with Singlet Oxygen |
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Sulfur reports,
Volume 19,
Issue 1,
1996,
Page 171-214
EdwardL. Clennan,
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PDF (1522KB)
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摘要:
The reactions of singlet oxygen with sulfides, sulfenamides, disulfides, and sulfenate esters will be critically discussed. The emphasis will be on the mechanistic details of these reactions.
ISSN:0196-1772
DOI:10.1080/01961779608047906
出版商:Taylor & Francis Group
年代:1996
数据来源: Taylor
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4. |
Synthesis and Reactivity of 3-Aminothiophenes and 3,4-Diaminothiophenes |
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Sulfur reports,
Volume 19,
Issue 1,
1996,
Page 215-284
Claude Paulmier,
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摘要:
Ten years ago, thiophenamines and thiophenediamines, usually called aminothiophenes and diaminothiophenes, were the subject of an important report.[1]3,4-Diaminothiophenes have also received separate attention.[2]For a long time,N-(2-thienyl)acetamide and alkyl 2-thienyl carbamates have been extensively studied, 2-aminothiophene itself being considered as very unstable. However, 2-aminothiophenes with electron-withdrawing substituents or functional groups are the subject of numerous papers.[1]
ISSN:0196-1772
DOI:10.1080/01961779608047907
出版商:Taylor & Francis Group
年代:1996
数据来源: Taylor
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5. |
Editorial board page for “Sulfur Reports”, Volume 19, Number 1 |
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Sulfur reports,
Volume 19,
Issue 1,
1996,
Page -
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PDF (57KB)
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摘要:
This is a scanned image of the original Editorial Board page(s) for this issue.
ISSN:0196-1772
DOI:10.1080/01961779608047903
出版商:Taylor & Francis Group
年代:1996
数据来源: Taylor
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