Synthesis of spiro〔2-cyclopentene-1,3'-imidazo〔1,2-a〕pyridine〕 derivatives and their interesting behavior in 1H-NMR spectra in deuteriochloroform
書誌事項
- タイトル別名
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- Synthesis of Spiro[2-cyclopentene-1,3’-imidazo[1,2-a]pyridine] Derivatives and Their Interesting Behavior in 1H-NMR Spectra in Deuteriochloroform
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抄録
Ethyl 2',3'-dihydro-2-methylthio-2',4-dioxospiro[2-cyclopentene-1,3'-imidazo[1,2-a]pyridine]-3-carboxylates were synthesized from the reactions of 3-[bis(methylthio)methylene]-2(3H)-imidazo[1,2-a]pyridinones with ethyl 4-chloroacetoacetate in the presence of a base. The 2-methylthio group in these Spiro compounds was easily replaced with some primary and secondary amines to afford the corresponding 2-amino derivatives. Very interestingly, the proton signals of these Spiro compounds in the H-1-NMR spectra in deuteriochloroform (CDCl3) changed with an increase in the sample concentration, and the analysis for the magnitude and the direction of each proton shift disclosed the conformational change of the cyclopentenone moiety in this molecule.
Article
HETEROCYCLES. 81(9):2075-2086 (2010)
収録刊行物
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- HETEROCYCLES
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HETEROCYCLES 81 (9), 2075-2086, 2010-09-01
The Japan Institute of Heterocyclic Chemistry
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詳細情報 詳細情報について
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- CRID
- 1050845763853034240
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- NII論文ID
- 120007104981
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- NII書誌ID
- AA00663739
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- ISSN
- 03855414
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- HANDLE
- 10091/10742
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- NDL書誌ID
- 10795058
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- 本文言語コード
- en
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- 資料種別
- journal article
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- データソース種別
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- IRDB
- NDL
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