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Volumn , Issue 13, 2006, Pages 2043-2046

Alkylidene[1,3]dithiolane-1,3-dioxides as potent Michael-type acceptors

Author keywords

Nucleophilic additions; Stereoelectronic effects; Sulfoxides; Thioacetals; Umpolung

Indexed keywords

2 BENZYLIDEN[1,3]DITHIOLANE; 2 BENZYLIDENE[1,3]DITHIOLANE 1,3 DIOXIDE; 3 [1,3 DIOXO[1,3]DITHIOLAN 2 YL] 1,3 DIPHENYL PROPAN 1 ONE; ACETAL DERIVATIVE; ACETOPHENONE; ACETOPHENONE DERIVATIVE; ACETOPHENONE ENOLATE; ALKYLIDENE[1,3]DITHIOLANE 1,3 DIOXIDE DERIVATIVE; METHANOL; PIPERIDINE; SULFOXIDE; THIOACETAL DERIVATIVE; THIOL DERIVATIVE; UNCLASSIFIED DRUG;

EID: 33748251264     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-948202     Document Type: Article
Times cited : (23)

References (33)
  • 13
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    • (2003) Angew. Chem. , vol.115 , pp. 5500
  • 23
    • 33646511337 scopus 로고    scopus 로고
    • Bäckvall, J.-E., Ed.; Wiley-VCH: Weinheim
    • (b) Further methods for the oxidation of sulfides are summarized in: Bäckvall, J.-E. In Modern Oxidation Methods; Bäckvall, J.-E., Ed.; Wiley-VCH: Weinheim, 2004, 193.
    • (2004) Modern Oxidation Methods , pp. 193
    • Bäckvall, J.-E.1
  • 28
    • 33748255581 scopus 로고    scopus 로고
    • note
    • 2-acetone (2:1) was used as eluent in the chromatography.
  • 29
    • 33748274390 scopus 로고    scopus 로고
    • CCDC 603241 (co-crystal of 3c and 7c) and CCDC 603242 (5c) contain the supplementary crystaltographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.