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dc.contributor.authorHuang, PQ
dc.contributor.author黄培强
dc.contributor.authorTang, X
dc.contributor.authorChen, AQ
dc.contributor.author陈安奇
dc.date.accessioned2012-06-22T00:29:37Z
dc.date.available2012-06-22T00:29:37Z
dc.date.issued2007-12-04
dc.identifier.citationSYNTHETIC COMMUNICATIONS,2000,30(13):2259-2268zh_CN
dc.identifier.issn0039-7911
dc.identifier.urihttp://dx.doi.org/doi:10.1080/00397910008086864
dc.identifier.urihttps://dspace.xmu.edu.cn/handle/2288/12925
dc.description.abstractA flexible approach to protected trans-5-alkyl-4-hydroxy-2-pyrrolidinones was described. The key step involved the alpha-amidoalkylation of benzenesulfone derived from (S)-malic acid, with organozinc reagents generated in situ from Grignard reagents and anhydrous ZnCl2. OEt2.zh_CN
dc.language.isoenzh_CN
dc.publisherMARCEL DEKKER INCzh_CN
dc.titleAn alternative stereoselective synthesis of protected trans-5-alkyl-4-hydroxy-2-pyrrolidinoneszh_CN
dc.typeArticlezh_CN


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