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Volumn 72, Issue 1, 2007, Pages 26-30

Mild and selective deprotection method of acetylated steroids and diterpenes by dibutyltin oxide

Author keywords

Deacetylation; Dibutyltin oxide; Diterpene; Regioselective reaction

Indexed keywords

3BETA,5ALPHA,6BETA TRIHYDROXYPREGN 16 EN 20 ONE; 3BETA,6BETA DI O ACETYL 5ALPHA HYDROXYPREGN 16 EN 20 ONE; ACETIC ACID DERIVATIVE; CARBONYL DERIVATIVE; DIBUTYLTIN OXIDE; DITERPENE; HYDROXYL GROUP; METHANOL; ORGANOTIN COMPOUND; STEROID; UNCLASSIFIED DRUG;

EID: 33845943238     PISSN: 0039128X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.steroids.2006.10.004     Document Type: Article
Times cited : (17)

References (24)
  • 2
    • 2442481817 scopus 로고    scopus 로고
    • Lipase-catalysed deacetylation of androstane and pregnane derivatives: influence of ring d substitution
    • Andrea C.B., and Alicia B. Lipase-catalysed deacetylation of androstane and pregnane derivatives: influence of ring d substitution. J Mol Catal B: Enzym 29 (2004) 149-153
    • (2004) J Mol Catal B: Enzym , vol.29 , pp. 149-153
    • Andrea, C.B.1    Alicia, B.2
  • 3
    • 0029040492 scopus 로고
    • Enzymatic deacetylation of steroids bearing labile functions
    • Alicia B., Marta S.M., and Eduardo G.G. Enzymatic deacetylation of steroids bearing labile functions. Tetrahedron Lett 25 36 (1995) 4349-4352
    • (1995) Tetrahedron Lett , vol.25 , Issue.36 , pp. 4349-4352
    • Alicia, B.1    Marta, S.M.2    Eduardo, G.G.3
  • 4
    • 0028914454 scopus 로고
    • Mild deprotection of steroids esters by bis(tributyltin)oxide
    • Marina G.P., and Marta S.M. Mild deprotection of steroids esters by bis(tributyltin)oxide. Tetrahedron Lett 19 36 (1995) 3311-3314
    • (1995) Tetrahedron Lett , vol.19 , Issue.36 , pp. 3311-3314
    • Marina, G.P.1    Marta, S.M.2
  • 5
    • 0029043869 scopus 로고
    • Microwave-induced organic reactions of bile acid; esterification, deformylation and deacetylation using mild reagents
    • Dayal B., Rao K., and Salen G. Microwave-induced organic reactions of bile acid; esterification, deformylation and deacetylation using mild reagents. Steroids 60 (1995) 453-457
    • (1995) Steroids , Issue.60 , pp. 453-457
    • Dayal, B.1    Rao, K.2    Salen, G.3
  • 6
    • 0035966604 scopus 로고    scopus 로고
    • Total synthesis of new steroids having an aromatic A ring with a 3-OH
    • Philippe M., Malika I.O., and Maurice S. Total synthesis of new steroids having an aromatic A ring with a 3-OH. Tetrahedron Lett 42 (2001) 847-849
    • (2001) Tetrahedron Lett , Issue.42 , pp. 847-849
    • Philippe, M.1    Malika, I.O.2    Maurice, S.3
  • 7
    • 0001367460 scopus 로고    scopus 로고
    • Microwave-promoted transformations: fast and chemoselective N-acylation of amino alcohols using catalytic amounts of dibutyltin oxide. Influence of the power output and the nature of the acylating agent on the selectivity
    • Morcuende A., and Ors M. Microwave-promoted transformations: fast and chemoselective N-acylation of amino alcohols using catalytic amounts of dibutyltin oxide. Influence of the power output and the nature of the acylating agent on the selectivity. J Org Chem 61 16 (1996) 5264-5270
    • (1996) J Org Chem , vol.61 , Issue.16 , pp. 5264-5270
    • Morcuende, A.1    Ors, M.2
  • 8
    • 0035477628 scopus 로고    scopus 로고
    • A mild and effective method for the transesterification of carboxylic acid esters
    • Baumhof P., Mazitschek R., and Giannis A. A mild and effective method for the transesterification of carboxylic acid esters. Angew Chem Int Ed 19 40 (2001) 3672-3674
    • (2001) Angew Chem Int Ed , vol.19 , Issue.40 , pp. 3672-3674
    • Baumhof, P.1    Mazitschek, R.2    Giannis, A.3
  • 9
    • 0030598046 scopus 로고    scopus 로고
    • Cleavage of carboxylic esters effected by organotin oxides and hydroxides under classical heating and microwave irradiation. A comparative study
    • Furlán R.L.E., Mata E.G., and Mascaretti O.A. Cleavage of carboxylic esters effected by organotin oxides and hydroxides under classical heating and microwave irradiation. A comparative study. Tetrahedron Lett 37 30 (1996) 5229-5232
    • (1996) Tetrahedron Lett , vol.37 , Issue.30 , pp. 5229-5232
    • Furlán, R.L.E.1    Mata, E.G.2    Mascaretti, O.A.3
  • 10
    • 0037064339 scopus 로고    scopus 로고
    • A mild and selective method for cleavage of O-acetyl groups with dibutyltin oxide
    • Liu H.M., Yan X.B., Li W., and Huang C.H. A mild and selective method for cleavage of O-acetyl groups with dibutyltin oxide. Carbohydr Res 337 19 (2002) 1763-1767
    • (2002) Carbohydr Res , vol.337 , Issue.19 , pp. 1763-1767
    • Liu, H.M.1    Yan, X.B.2    Li, W.3    Huang, C.H.4
  • 11
    • 4644347258 scopus 로고    scopus 로고
    • Syntheses of acetylated steroid glycisides and selective cleavage of O-acetyl groups in sugar moiety
    • Wang S.M., Ge W.Z., Liu H.M., Zou D.P., and Yan X.B. Syntheses of acetylated steroid glycisides and selective cleavage of O-acetyl groups in sugar moiety. Steroids 69 (2004) 599-604
    • (2004) Steroids , Issue.69 , pp. 599-604
    • Wang, S.M.1    Ge, W.Z.2    Liu, H.M.3    Zou, D.P.4    Yan, X.B.5
  • 12
    • 0016184522 scopus 로고
    • Phytochemical investigation of Xanthium spinosum L
    • Metwally A.M., Khafagy S.M., and el-Naggar S.F. Phytochemical investigation of Xanthium spinosum L. Pharmazie 29 6 (1974) 415-417
    • (1974) Pharmazie , vol.29 , Issue.6 , pp. 415-417
    • Metwally, A.M.1    Khafagy, S.M.2    el-Naggar, S.F.3
  • 13
    • 0017625719 scopus 로고
    • 4-Desmethylsgerols in the seeds of Solanaceae
    • Itoh T., Tamura T., and Matsumoto T. 4-Desmethylsgerols in the seeds of Solanaceae. Steroids 30 3 (1977) 425-433
    • (1977) Steroids , vol.30 , Issue.3 , pp. 425-433
    • Itoh, T.1    Tamura, T.2    Matsumoto, T.3
  • 14
    • 0013797563 scopus 로고
    • Microbiological transformation of dehydroepiandrosterone, progesterone, desoxycorticosterone, and testosterone by Gibberella saubinetti
    • Okada M., Yamada A., and Ishidate M. Microbiological transformation of dehydroepiandrosterone, progesterone, desoxycorticosterone, and testosterone by Gibberella saubinetti. Yakugaku Zasshi 85 9 (1965) 816-822
    • (1965) Yakugaku Zasshi , vol.85 , Issue.9 , pp. 816-822
    • Okada, M.1    Yamada, A.2    Ishidate, M.3
  • 15
    • 0347352763 scopus 로고    scopus 로고
    • Research development of rabdosia rubescens
    • Liu C.J., and Zhao Z.H. Research development of rabdosia rubescens. Chin Pharm J 33 10 (1998) 577-581
    • (1998) Chin Pharm J , vol.33 , Issue.10 , pp. 577-581
    • Liu, C.J.1    Zhao, Z.H.2
  • 16
    • 33845962319 scopus 로고    scopus 로고
    • Isolation and structure analysis of the biologically active components of the andrographis on earth surface
    • Wang J.L., and Zhang S.J. Isolation and structure analysis of the biologically active components of the andrographis on earth surface. J Qiqihar Univ 15 2 (1999) 50-52
    • (1999) J Qiqihar Univ , vol.15 , Issue.2 , pp. 50-52
    • Wang, J.L.1    Zhang, S.J.2
  • 17
    • 0029927107 scopus 로고    scopus 로고
    • Differential behavior of (25R)-5,6,-epoxyspirostan-22α-O-3β-ol and (25R)-5,6-epoxyspirostan-22α-O-3β,4β-diol toward dowex
    • Korde S.S., Baig M.H.A., Desai U.R., and Trivedi G.K. Differential behavior of (25R)-5,6,-epoxyspirostan-22α-O-3β-ol and (25R)-5,6-epoxyspirostan-22α-O-3β,4β-diol toward dowex. Steroids 61 5 (1996) 290-295
    • (1996) Steroids , vol.61 , Issue.5 , pp. 290-295
    • Korde, S.S.1    Baig, M.H.A.2    Desai, U.R.3    Trivedi, G.K.4
  • 18
    • 0038102459 scopus 로고    scopus 로고
    • 1α, 3β, 5β-Trihydroxy-24-methylenecholestan-6-one: a noval steroid from a soft coral sinularia gibberosa
    • Ahmed A.F., Dai C.F., Kuo Y.H., and Sheu J.H. 1α, 3β, 5β-Trihydroxy-24-methylenecholestan-6-one: a noval steroid from a soft coral sinularia gibberosa. Steroids 68 4 (2003) 377-381
    • (2003) Steroids , vol.68 , Issue.4 , pp. 377-381
    • Ahmed, A.F.1    Dai, C.F.2    Kuo, Y.H.3    Sheu, J.H.4
  • 19
    • 4644330922 scopus 로고    scopus 로고
    • Advance in the research of marine steroids
    • Tang H.F., Yi Y.H., and Yao X.S. Advance in the research of marine steroids. Chin J Mar Drugs 21 3 (2002) 38-47
    • (2002) Chin J Mar Drugs , vol.21 , Issue.3 , pp. 38-47
    • Tang, H.F.1    Yi, Y.H.2    Yao, X.S.3
  • 20
    • 0000828185 scopus 로고
    • Recent developments in the marine sterol field
    • Dierassi C. Recent developments in the marine sterol field. Pure Appl Chem 53 (1981) 873-890
    • (1981) Pure Appl Chem , vol.53 , pp. 873-890
    • Dierassi, C.1
  • 21
    • 0034045851 scopus 로고    scopus 로고
    • Polyhydroxylated sterols from the octocoral Dendronephthya gigantean
    • Yoshikawa K., Kanekuni S., Hanahusa M., Arihara S., and Ohta T. Polyhydroxylated sterols from the octocoral Dendronephthya gigantean. J Nat Prod 63 5 (2000) 670-672
    • (2000) J Nat Prod , vol.63 , Issue.5 , pp. 670-672
    • Yoshikawa, K.1    Kanekuni, S.2    Hanahusa, M.3    Arihara, S.4    Ohta, T.5
  • 22
    • 0034891542 scopus 로고    scopus 로고
    • Anoval sterol from Chinese truffles tuber indicum
    • Gao J.M., Hu L., and Liu J.K. Anoval sterol from Chinese truffles tuber indicum. Steroids 66 10 (2001) 771-775
    • (2001) Steroids , vol.66 , Issue.10 , pp. 771-775
    • Gao, J.M.1    Hu, L.2    Liu, J.K.3
  • 24
    • 0032862255 scopus 로고    scopus 로고
    • Steroids from sponges: recent reports
    • Aiello A., Fattorusso E., and Menna M. Steroids from sponges: recent reports. Steroids 64 10 (1999) 687-714
    • (1999) Steroids , vol.64 , Issue.10 , pp. 687-714
    • Aiello, A.1    Fattorusso, E.2    Menna, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.