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Volumn 5, Issue 8, 2003, Pages 1317-1320

Improved synthesis of tert-butanesulfinamide suitable for large-scale production

Author keywords

[No Author keywords available]

Indexed keywords

ACETONE; ALCOHOL DERIVATIVE; SOLVENT; SULFINAMIDE; TERT BUTANESULFINAMIDE; UNCLASSIFIED DRUG;

EID: 0141628885     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol034254b     Document Type: Article
Times cited : (157)

References (33)
  • 5
    • 0141437625 scopus 로고    scopus 로고
    • Ref 3b
    • (a) Ref 3b.
  • 18
    • 0141772490 scopus 로고    scopus 로고
    • See ref 7b
    • See ref 7b.
  • 27
    • 0141660572 scopus 로고    scopus 로고
    • note
    • Cost for the available (S)-enantiomer is $45/g or more.
  • 30
    • 0141772489 scopus 로고    scopus 로고
    • note
    • Both enantiomers are commercially available for ∼$15/g.
  • 31
    • 0037181367 scopus 로고    scopus 로고
    • See Supporting Information
    • Ruck, R. T.; Jacobsen, E. N. J. Am. Chem. Soc. 2002, 124, 2882-2883. See Supporting Information.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 2882-2883
    • Ruck, R.T.1    Jacobsen, E.N.2
  • 32
    • 0141549179 scopus 로고    scopus 로고
    • note
    • Crystallized from 5 mL of hexanes/g of sulfinamide.
  • 33
    • 0141772488 scopus 로고    scopus 로고
    • note
    • Crystallization from 10 mL of hexanes/g of sulfinamide provides enantiopure material (minor enantiomer not detectable) in 60% overall yield.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.