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Volumn 36, Issue 13, 2006, Pages 1911-1914

Deacetylation of thioacetate using acetyl chloride in methanol

Author keywords

Acetyl chloride; Carbapenem intermediate; Deacetylation; Thioacetate; Thiol

Indexed keywords

ACETIC ACID DERIVATIVE; ACETYL CHLORIDE; METHANOL; THIOACETATE; UNCLASSIFIED DRUG;

EID: 33745009294     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910600602735     Document Type: Article
Times cited : (15)

References (11)
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    • A highly efficient and useful synthetic protocol for the cleavage of tert-butyldimethylsilyl (TBS) ethers using a catalytic amount of acetyl chloride in dry methanol
    • Khan, A. T.; Mondal, E. A highly efficient and useful synthetic protocol for the cleavage of tert-butyldimethylsilyl (TBS) ethers using a catalytic amount of acetyl chloride in dry methanol. Synlett 2003, 694-698.
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    • Khan, A.T.1    Mondal, E.2
  • 7
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    • Acetyl chloride-methanol as a convenient reagent for A) Quantitative formation of aminehydrochlorides, B Carboxylate ester formation, C Mild removal of N-t-Boc protective group
    • Nudelman, A.; Bechor, Y.; Flab, E.; Fisher, B.; Wexler, B. A.; Nudelmen, A. Acetyl chloride-methanol as a convenient reagent for A) Quantitative formation of aminehydrochlorides, B) Carboxylate ester formation, C) Mild removal of N-t-Boc protective group. Synth. Commun. 1998, 28, 471-474.
    • (1998) Synth. Commun. , vol.28 , pp. 471-474
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    • Mild and chemoselective deacetylation method using a catalytic amount of acetyl chloride in methanol
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.