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Volumn , Issue 25, 2009, Pages 4357-4364

Versatile synthesis of secondary 2-amino thiols and/or their disulfides via thiazolinium salts

Author keywords

Alkylation; Amino alcohols; Amino thiols; Heterocycles; Sulfur

Indexed keywords


EID: 68949142767     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200900514     Document Type: Article
Times cited : (15)

References (32)
  • 28
    • 65249090179 scopus 로고    scopus 로고
    • For a review dealing with 2-thiazolines, see
    • For a review dealing with 2-thiazolines, see: A.-C. Gaumont, M. Gulea, J. Levillain, Chem. Rev. 2009, 109, 1371.
    • (2009) Chem. Rev , vol.109 , pp. 1371
    • Gaumont, A.-C.1    Gulea, M.2    Levillain, J.3
  • 29
    • 68949125888 scopus 로고    scopus 로고
    • The acid hydrolysis of a thiazolinium salt leading to N-methylcysteine has already been reported, but the yield was not given: K. Undheim, A. Aidem, Acta Chem. Scand. 1970, 24, 3129.
    • The acid hydrolysis of a thiazolinium salt leading to N-methylcysteine has already been reported, but the yield was not given: K. Undheim, A. Aidem, Acta Chem. Scand. 1970, 24, 3129.
  • 30
    • 68949083969 scopus 로고    scopus 로고
    • The use of only 1 equiv. of MsCl led to a mixture of compounds difficult to separate and characterize.
    • The use of only 1 equiv. of MsCl led to a mixture of compounds difficult to separate and characterize.
  • 32
    • 68949106400 scopus 로고    scopus 로고
    • 2O was used instead of MsCl in the reaction with 3b. The conversion of the 2-[(trifluoromethyl- carbonyl)methylidene]thiazolidine into amino thiol 5b was still incomplete even after 3 d under acid hydrolysis conditions.
    • 2O was used instead of MsCl in the reaction with 3b. The conversion of the 2-[(trifluoromethyl- carbonyl)methylidene]thiazolidine into amino thiol 5b was still incomplete even after 3 d under acid hydrolysis conditions.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.