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Volumn 15, Issue 28, 1974, Pages 2421-2424

Crown ether catalysis: "naked" anions as reactive intermediates in the synthesis of phenacyl esters

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Indexed keywords


EID: 0041916183     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(01)92274-9     Document Type: Article
Times cited : (87)

References (15)
  • 7
    • 49649134485 scopus 로고
    • Peterson's Nomenclature. Dicyclohexyl-18-crown-6 is 2,3,11,12-dicyclohexyl-1,4,7,10,13,16-hexaoxacyclooctadecane. This material is available from Aldrich Chemical Co., Milwaukee, Wis., 53233. 18-crown-6 is 1,4,7,10,13,16-hexaoxacyclooctadecane and can be synthesized according to the procedure of, or by that of G.W. Gokel and D.J. Cram, Department of Chemistry, University of California at Los Angeles, Org. Syn., submitted.
    • (1972) Tetrahedron Letters , pp. 1793
    • Greene1
  • 10
    • 84918291316 scopus 로고    scopus 로고
    • C.L. Liotta, personal communication, 1973.
  • 11
    • 84918291315 scopus 로고
    • The removal of the phenacyl protecting group is accomplished by stirring the derivative with Zn in acetic acid at room temperature for 1-2 hours. Filtration and workup gives the carboxylic acid in 90-100% yield.
    • (1973) Tetrahedron Letters. , vol.343
    • Hendrickson1    Kandall2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.