메뉴 건너뛰기




Volumn 60, Issue 7, 2004, Pages 1587-1599

An effective method for the synthesis of carboxylic esters and lactones using substituted benzoic anhydrides with Lewis acid catalysts

Author keywords

3,5 Bis(trifluoromethyl)benzoic anhydride; 4 (Trifluoromethyl)benzoic anhydride; Carboxylic esters; Cephalosporolide D; Lewis acid catalysts; Macrolactones; Medium sized lactones; Mixed anhydrides

Indexed keywords

3,5 BIS(TRIFLUOROMETHYL)BENZOIC ANHYDRIDE; ACID ANHYDRIDE; ALCOHOL DERIVATIVE; BENZOIC ACID; CARBOXYLIC ACID DERIVATIVE; CHLOROTRIMETHYLSILANE; ESTER DERIVATIVE; LACTONE DERIVATIVE; LEWIS ACID; SILANE DERIVATIVE; TITANIUM; TITANIUM DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0742306830     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2003.12.013     Document Type: Article
Times cited : (85)

References (107)
  • 1
    • 0001674034 scopus 로고
    • For a review, see: (a). B.M. Trost, & I. Fleming. Oxford: Pergamon
    • For a review, see: (a) Mulzer J. Trost B.M., Fleming I. Comprehensive organic synthesis. Vol. 6:1991;323-380 Pergamon, Oxford.
    • (1991) Comprehensive Organic Synthesis , vol.6 , pp. 323-380
    • Mulzer, J.1
  • 66
    • 85030894165 scopus 로고    scopus 로고
    • Shoda, S. PhD Thesis, the University of Tokyo, 1980
    • Shoda, S. PhD Thesis, the University of Tokyo, 1980.
  • 77
  • 98
    • 0742316365 scopus 로고    scopus 로고
    • 2 were effective catalysts for the synthesis of carboxylic esters in 1992. See, Ref. 5a,b
    • 2 were effective catalysts for the synthesis of carboxylic esters in 1992. See, Ref. 5a,b.
    • (2000) Lewis Acids in Organic Synthesis , vol.2 , pp. 865-881
    • Hara, R.1    Takahashi, T.2
  • 99
    • 0034953235 scopus 로고    scopus 로고
    • Recently, Buszek et al. also reported monomer-selective lactonization for the synthesis of an 8-membered ring lactone moiety of octalactins and cephalosporolide D using S-Py ester method
    • Recently, Buszek et al. also reported monomer-selective lactonization for the synthesis of an 8-membered ring lactone moiety of octalactins and cephalosporolide D using S-Py ester method Buszek K.R., Jeong Y., Sato N., Still P.C., Muino P.L., Ghosh I. Synth. Commun. 31:2001;1781-1791.
    • (2001) Synth. Commun. , vol.31 , pp. 1781-1791
    • Buszek, K.R.1    Jeong, Y.2    Sato, N.3    Still, P.C.4    Muino, P.L.5    Ghosh, I.6
  • 100
    • 0036012057 scopus 로고    scopus 로고
    • Quite recently, we developed an alternative mixed-anhydride method using 2-methyl-6-nitrobenzoic anhydride (MNBA) by the promotion of basic catalysts. These methods promoted by acids or bases could be complementarily utilized for the synthesis of carboxylic esters and lactones according to the stability of substrates and products under the reaction conditions. (a)
    • Quite recently, we developed an alternative mixed-anhydride method using 2-methyl-6-nitrobenzoic anhydride (MNBA) by the promotion of basic catalysts. These methods promoted by acids or bases could be complementarily utilized for the synthesis of carboxylic esters and lactones according to the stability of substrates and products under the reaction conditions. (a) Shiina I., Ibuka R., Kubota M. Chem. Lett. 2002;286-287.
    • (2002) Chem. Lett. , pp. 286-287
    • Shiina, I.1    Ibuka, R.2    Kubota, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.