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Volumn 124, Issue 51, 2002, Pages 15172-15173

Ruthenium-catalyzed propargylic substitution reaction of propargylic alcohols with thiols: A general synthetic route to propargylic sulfides

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL DERIVATIVE; ALKYNE; FUNCTIONAL GROUP; PROPARGYLIC ALCOHOL DERIVATIVE; RUTHENIUM; SULFIDE; THIOL DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0037176276     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja027754t     Document Type: Article
Times cited : (126)

References (24)
  • 10
    • 0012151303 scopus 로고    scopus 로고
    • note
    • 2RuCp*Cl] were ineffective for the propargylic substitution reaction.
  • 11
    • 0012152139 scopus 로고    scopus 로고
    • note
    • Unfortunately, no propargylic substitution reactions of 2a with alcohols, amines, acetone, and silyl enol ethers in the presence of 1e occurred under similar reaction conditions.
  • 12
    • 0012193373 scopus 로고    scopus 로고
    • note
    • In contrast to the reaction of 2.4-diphenyl-3-butyn-2-ol (2h) (Table 2, run 14), the reaction of 1,1,3-triphenyl-2-propyn-1-ol with "BuSH at 60 °C for 16 h afforded not the corresponding propargylic product but 1,3,3- triphenyl-2-propen-1-one in 80% yield as a sole product.
  • 13
    • 0012114329 scopus 로고    scopus 로고
    • note
    • 12
  • 14
    • 0012113895 scopus 로고    scopus 로고
    • note
    • When -4a was treated with "BuSH at room temperature, racemic 5aa was formed.
  • 17
  • 19
    • 33845281351 scopus 로고
    • and references therein
    • Nicholas, K. M. Acc. Chem. Res. 1987, 20, 207 and references therein.
    • (1987) Acc. Chem. Res. , vol.20 , pp. 207
    • Nicholas, K.M.1
  • 23
    • 0034251445 scopus 로고    scopus 로고
    • and references therein
    • (a) Kondo, T.; Mitsudo, T. Chem. Rev. 2000, 100, 3205 and references therein.
    • (2000) Chem. Rev. , vol.100 , pp. 3205
    • Kondo, T.1    Mitsudo, T.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.