Syntheses and Configuration Inversion of Substituted Oxazolines  

Syntheses and Configuration Inversion of Substituted Oxazolines

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作  者:YANG Shao-rong HU Quan-yuan LIU Jun YANG Hui HU Xian-ming 

机构地区:[1]College of Chemistry,Wuhan University,Wuhan 430072,P.R.China

出  处:《Chemical Research in Chinese Universities》2001年第3期271-275,共5页高等学校化学研究(英文版)

基  金:Supported by the Science and Technology Fundation of Wuhan City and Wuhan Red Heart K(Group) Co. Ltd.

摘  要:The present paper covers the simply and highly stereoselective syntheses of (α-S, 4S)-2-dichloromethyl-4, 5-dihydro-α-(4-nitrophenyl)-4-oxazolemethanol (4a), (α-S, 4S)-2-methyl-4, 5-dihydro-α-(4-nitrophenyl)-4-oxazolemethanol (4b), and (α-R, 4R)-2-dichloromethyl-4, 5-dihydro-α-[(4-methylsulfonyl)phenyl]-4-oxazolemethanol(4c) with good yields(80%—90%). A configuration inversion product, (1R, 2S)-2-dichloroacetamido-1-(4-nitrophenyl)-1, 3-propanediol (8), was obtained during our attempting to convert compound 4a into (4S, 5R)-2-(dichloromethyl)-4, 5-dihydro-5-(4-nitrophenyl)-4-oxazolemethanol(7).The present paper covers the simply and highly stereoselective syntheses of (α-S, 4S)-2-dichloromethyl-4, 5-dihydro-α-(4-nitrophenyl)-4-oxazolemethanol (4a), (α-S, 4S)-2-methyl-4, 5-dihydro-α-(4-nitrophenyl)-4-oxazolemethanol (4b), and (α-R, 4R)-2-dichloromethyl-4, 5-dihydro-α-[(4-methylsulfonyl)phenyl]-4-oxazolemethanol(4c) with good yields(80%—90%). A configuration inversion product, (1R, 2S)-2-dichloroacetamido-1-(4-nitrophenyl)-1, 3-propanediol (8), was obtained during our attempting to convert compound 4a into (4S, 5R)-2-(dichloromethyl)-4, 5-dihydro-5-(4-nitrophenyl)-4-oxazolemethanol(7).

关 键 词:OXAZOLINE HETEROCYCLIC Configuration inversion 

分 类 号:O626.2[理学—有机化学]

 

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