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Reaction of 2,3-Dihydro-1,5-benzothiazepines and Phenylacetyl Chloride in the Presence of Triethylamine:A New Aspect on the Formation Mechanism of Dihydro-1,3-oxazin-4-one Derivatives 被引量:1
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作者 许家喜 王超 张奇涵 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2004年第9期1012-1018,共7页
2a,4-Disubstituted 2,2a,3,4-tetrahydro-2-phenyl-1H-azeto[2,1-d][1,5]benzothiazepin-1-ones, as well as 2-substi- tuted 2,3-dihydro-3-phenylacetyl-2-styryl-benzothiazoles and 4a,6-disubstituted 3-benzyl-4a,5-dihydro-2-p... 2a,4-Disubstituted 2,2a,3,4-tetrahydro-2-phenyl-1H-azeto[2,1-d][1,5]benzothiazepin-1-ones, as well as 2-substi- tuted 2,3-dihydro-3-phenylacetyl-2-styryl-benzothiazoles and 4a,6-disubstituted 3-benzyl-4a,5-dihydro-2-phenyl- 1H,6H-[1,3]oxazino[2,3-d][1,5]benzothiazepin-1-ones, were obtained from the reaction of 2,4-disubstituted 2,3-dihydro-1,5-benzothiazepines with phenylacetyl chloride in the presence of triethylamine. The mechanism for the formation of 4a,5-dihydro-1H,6H-[1,3]oxazino[2,3-d][1,5]benzothiazepin-1-ones, 2,3-dihydro-1,3-oxazin-4-one derivatives, was suggested. 展开更多
关键词 1 5-benzothiazepine 2 2a 3 4-tetrahydro-1h-azeto[2 1-d][1 5]benzothiazepin-1-one 2 3-dihydro- benzothiazole 4a 5-dihydro-1h 6h-[1 3]oxazino[2 3-d][1 5]benzothiazepin-1-one cycloaddition mechanism
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A New Halogenated Biindole and A New Apo-carotenone from Green Alga Chaetomorpha basiretorsa Setchell 被引量:6
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作者 DaYongSHI LiJunHAN +5 位作者 JieSUN ShuaiLI SuJuanWANG YongChunYANG XiaoFAN JianGongSHI 《Chinese Chemical Letters》 SCIE CAS CSCD 2005年第6期777-780,共4页
A new halogenated biindole and a new apo-carotenone have been isolated from the ethanolic extract of the green alga Chaetomorpha basiretorsa Sethcell. On the basis of chemical and spectroscopic methods including 2D NM... A new halogenated biindole and a new apo-carotenone have been isolated from the ethanolic extract of the green alga Chaetomorpha basiretorsa Sethcell. On the basis of chemical and spectroscopic methods including 2D NMR technique, their structures have been elucidated as 4,4′-dichloro-5,5′-dibromo-7,7′-dimethoxy-2,2′-bi-1H-indole and 1′S*,4′R*-8-(4′-hydroxy-2′,6′,6′- trimethylcyclohex-2-enyl)-6-methyloct-3E,5E,7E-trien-2-one, respectively. 展开更多
关键词 Green alga Chaetomorpha basiretorsa Sethcell 4 4′-dichloro-5 5′-dibromo-7 7′-di- methoxy-2 2′-bi-1h-indole 1′S* 4′R*-8-(4′-hydroxy-2′ 6 6′-trimethylcyclohex-2-enyl)-6-methyl- oct-3E 5E 7E-trien-2-one.
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Biomimetic transformation of gentiopicroside to erythrocentaurin 被引量:2
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作者 Cui Ling Wang Jian Li Liu +2 位作者 Zhu Lan Liu Xin Sheng Li Xiao Yong Cao 《Chinese Chemical Letters》 SCIE CAS CSCD 2009年第2期150-152,共3页
Biomimetic transformation of gentiopicroside was carded out by β-glucosidase at pH 7.0 for 3 days at 37 ℃. Two products, erythrocentaurin and 5,6-dihydro-5-formyl-6-methyl-1H,3H-pyrano[3,4-c]pyran-1-one were isolate... Biomimetic transformation of gentiopicroside was carded out by β-glucosidase at pH 7.0 for 3 days at 37 ℃. Two products, erythrocentaurin and 5,6-dihydro-5-formyl-6-methyl-1H,3H-pyrano[3,4-c]pyran-1-one were isolated and identified by ^1H NMR, ^13C NMR, UV, IR, MS and elemental analyse. The possible mechanisms were discussed. 展开更多
关键词 GENTIOPICROSIDE Biomimetic transformation Β-GLUCOSIDASE Erythrocentaurin 5 6-Dihydro-5-formyl-6-methyl-1h 3h-pyrano[3 4-c]pyran-1-one
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