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Volumn 34, Issue 3, 2004, Pages 533-540

Stereoselective Addition of Pyridyl Lithium to 22-Aldehyde Steroid. Synthesis of 22-Piperidin-yl-pregnan-3β, 22(S)-diol

Author keywords

22 Aldehyde steroid; Azasterols; Pyridyl lithium

Indexed keywords

22 ALDEHYDE STEROID; 22 PIPERIDIN YLPREGNAN 3BETA,22 DIOL; 22 PIPERIDIN YLPREGNAN 5 EN 3BETA,22 OL; 23,24 BISNOR 5 CHOLENIC ACID 3BETA OL; 3BETA TETRAHYDROPYRANYLOXY 23 BISNORCHOL 5 EN 22 AL; ALDEHYDE; LITHIUM DERIVATIVE; PYRIDYL LITHIUM; STEROID; UNCLASSIFIED DRUG;

EID: 1542346116     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1081/SCC-120027294     Document Type: Article
Times cited : (4)

References (16)
  • 4
    • 0031172883 scopus 로고    scopus 로고
    • 24(28)-sterol methyl transferase from Saccharomyces cerevisiae
    • 24(28)-sterol methyl transferase from Saccharomyces cerevisiae. Arch. Biochem. Biophys. 1997, 342 (1), 68-81.
    • (1997) Arch. Biochem. Biophys. , vol.342 , Issue.1 , pp. 68-81
    • Nes, W.D.1    Guo, D.2    Wen, Z.3
  • 5
    • 2142858450 scopus 로고
    • High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids
    • Ohtani, I.; Kusumi, T.; Kashman, Y.; Kakisawa, H. High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids. J. Am. Chem. Soc. 1991, 113, 4092-4096.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 4092-4096
    • Ohtani, I.1    Kusumi, T.2    Kashman, Y.3    Kakisawa, H.4
  • 6
    • 49949128203 scopus 로고
    • Torsional strain involving partial bonds. The stereochemistry of the lithium aluminiun hydride reduction of some simple open-chain ketones
    • Chérest, M.; Felkin, H.; Prudent, N. Torsional strain involving partial bonds. The stereochemistry of the lithium aluminiun hydride reduction of some simple open-chain ketones. Tetrahedron Lett. 1968, 18, 2199-2204.
    • (1968) Tetrahedron Lett. , vol.18 , pp. 2199-2204
    • Chérest, M.1    Felkin, H.2    Prudent, N.3
  • 7
    • 0002451214 scopus 로고
    • Theoretical interpretation of 1-2 asymmetric induction. The importance of antiperiplanarity
    • Anh, N.T.; Eisenstein, O. Theoretical interpretation of 1-2 asymmetric induction. The importance of antiperiplanarity. Nouv. J. de Chim. 1977, 1 (1), 61-70.
    • (1977) Nouv. J. De Chim. , vol.1 , Issue.1 , pp. 61-70
    • Anh, N.T.1    Eisenstein, O.2
  • 8
    • 49149146087 scopus 로고
    • Stereocontrol in the synthesis of acyclic systems: Applications to natural product synthesis
    • Bartlett, P.A. Stereocontrol in the synthesis of acyclic systems: applications to natural product synthesis. Tetrahedron 1980, 36, 3-72.
    • (1980) Tetrahedron , vol.36 , pp. 3-72
    • Bartlett, P.A.1
  • 9
    • 0017806247 scopus 로고
    • Various approaches to the construction of aliphatic side chains of steroids and related compounds
    • Piatak, D.M.; Wicha. Various approaches to the construction of aliphatic side chains of steroids and related compounds. J. Chem. Rev. 1978, 78 (3), 199-241.
    • (1978) J. Chem. Rev. , vol.78 , Issue.3 , pp. 199-241
    • Piatak, D.M.1    Wicha2
  • 10
    • 0015270358 scopus 로고
    • Some stereoselective and regioselective olefin additions: Iodoacetoxylation and realted electrophilic additions across the 22(23)-bond of 3α,5α-cycloergosta-7,22-dien-6-one
    • Barton, D.H.R.; Poyser, J.P.; Sammes, P.G. Some stereoselective and regioselective olefin additions: iodoacetoxylation and realted electrophilic additions across the 22(23)-bond of 3α,5α -cycloergosta-7,22-dien-6-one. J. Chem. Soc., Perkin Trans. 1972, 1, 61.
    • (1972) J. Chem. Soc., Perkin Trans. , vol.1 , pp. 61
    • Barton, D.H.R.1    Poyser, J.P.2    Sammes, P.G.3
  • 11
    • 0016008144 scopus 로고
    • Stereospecific synthesis of (22R)-22-hydroxycholesterol and (22R)-cholesta-5,24-diene-3β,22-diol
    • Poyser, J.P.; Ourisson, G. Stereospecific synthesis of (22R)-22-hydroxycholesterol and (22R)-cholesta-5,24-diene-3β,22-diol. J. Chem. Soc., Perkin Trans. 1974, 1, 2061-2066.
    • (1974) J. Chem. Soc., Perkin Trans. , vol.1 , pp. 2061-2066
    • Poyser, J.P.1    Ourisson, G.2
  • 12
    • 0009663849 scopus 로고
    • The stereospecific synthesis of inotodiol 3β ,22R-dihydroxylanosta-8,24-diene
    • Poyser, J.P.; Reinach-Hirtzbach, F.; Ourisson, G. The stereospecific synthesis of inotodiol 3β,22R-dihydroxylanosta-8,24-diene. Tetrahedron 1974, 30, 977-986.
    • (1974) Tetrahedron , vol.30 , pp. 977-986
    • Poyser, J.P.1    Reinach-Hirtzbach, F.2    Ourisson, G.3
  • 15
    • 0034672702 scopus 로고    scopus 로고
    • Sterol methyl transferase: Enzymology and inhibition
    • David Nes, W. Sterol methyl transferase: enzymology and inhibition. Biochim. Biophys. Acta 2000, 1529, 63-88.
    • (2000) Biochim. Biophys. Acta , vol.1529 , pp. 63-88
    • David Nes, W.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.