Synthesis of 4-amino-5H-1,2-oxathiole 2,2-dioxides by cyclization of cyanohydrin mesylates.: New routes to β-amino and βketo sulfonic acids (vol 62, pg 7021, 1997)

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作者：

Poszávácz, L

Simig, G

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JOURNAL OF ORGANIC CHEMISTRY | 1998年 / 63卷 / 06期

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D O I：

10.1021/jo974034+

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

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页码：2052 / 2052

页数：1

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[1] Synthesis of 4-amino-5H-1,2-oxathiole 2,2-dioxides by cyclization of cyanohydrin mesylates. New routes to beta-amino and beta-keto sulfonic acids
Poszavacz, L
Simig, G
[J]. JOURNAL OF ORGANIC CHEMISTRY, 1997, 62 (20): : 7021 - 7023
[2] Studies into the synthesis of derivatives of 4-amino-2,3-dihydroisothiazole 1,1-dioxides and 4-amino-1,2-oxathiole 2,2-dioxides: The search for linked pi-system containing analogues as potential inhibitors of HIV-1 reverse transcriptase
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[3] REACTION OF SULFENE AND DICHLOROKETENE WITH OPEN-CHAIN N,N-DISUBSTITUTED ALPHA-AMINOMETHYLENEKETONES - SYNTHESIS OF N,N-DISUBSTITUTED 4-AMINO-3,4-DIHYDRO-(5-METHYL-6-PHENYL)(5,6-DIPHENYL)-1,2-OXATHIIN 2,2-DIOXIDES AND OF 4-AMINO-3-CHLORO-5-METHYL-6-PHENYL-2H-PYRAN-2-ONES
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[4] REACTION OF SULFENE AND DICHLOROKETENE WITH OPEN-CHAIN N,N-DISUBSTITUTED ALPHA-AMINOMETHYLENEKETONES - SYNTHESIS OF 4-DIALKYLAMINO-3,4-DIHYDRO-6-METHYL-5-PHENYL-1,2-OXATHIIN 2,2-DIOXIDES AND OF N,N-DISUBSTITUTED 4-AMINO-3-CHLORO-(6-METHYL-5-PHENYL)(6-BENZYL)-2H-PYRAN-2-ONES
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