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Bibliographic Information
- Other Title
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- 二官能性炭素の反応およびその合成化学への利用
- 2カンノウセイ タンソ ノ ハンノウ オヨビ ソノ ゴウセイ カガク エ ノ
Search this article
Description
As are known by various sorts of the representative methylene type the bifunctional carbons, which signify the carbons linking two heterofunctional groups, have proved to furnish characteristic reactivities. That is to say, they can undergo easy substitution of their one-side group and receive insertion of unsatureted spieces into their one-side bond. The aim of author's investigation in this field was to develop basic reactions as well as new reagents which are useful for practicing organic chemists. This article is to review the work in this laboratory, which is constituted of numerous new reactions involving reduction, substitution, carbon-carbon bond formation, rearrangement, insertion, 1, 3-dipolar cycloaddition and so on, with development of new reagents such as formic acid-triethylamine azeotrope as a reducing agent, diazoalkane-generating agent and aromatic diazotategenerating agent. Application of the reactions to the syntheses of some physiologically active compounds is also briefly summarized.
Journal
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- YAKUGAKU ZASSHI
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YAKUGAKU ZASSHI 104 (3), 205-221, 1984
The Pharmaceutical Society of Japan
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Keywords
- bifunctional carbon
- catalytic hydrogenolysis
- formic acid reduction
- sodium borohydride reduction
- α-amidoalkylation
- N-alkylamidomethylation
- secondary aminomethylation
- primary aminomethylation
- ring closure
- β-lactam
- phenylthiomethylation
- decarboxylation reaction
- insertion reaction
- rearrangement reaction
- diazoalkane-generating agent
- aromatic diazotate-generating agent
- alkanesulfinate
- alkanesulfinyl chloride
- alkanesulfenyl chloride
- 1, 3-dipolar cycloaddition
- pyrrolizidine alkaloid
- formic acid-triethylamine azeotrope
Details 詳細情報について
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- CRID
- 1390001206127286656
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- NII Article ID
- 110003650616
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- NII Book ID
- AN00284903
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- ISSN
- 13475231
- 00316903
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- NDL BIB ID
- 2989630
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- Data Source
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- JaLC
- NDL Search
- Crossref
- CiNii Articles
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- Abstract License Flag
- Disallowed