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Volumn 6, Issue 4, 2011, Pages 477-490

Drimenol: A versatile synthon for compounds with trans-drimane skeleton

Author keywords

Ambergris related compounds; Chiral synthon; Drimane terpenoids; Drimenol; Sesquiterpenes

Indexed keywords

DRIMANE TERPENOID DERIVATIVE; DRIMENOL; NATURAL PRODUCT; SESQUITERPENE DERIVATIVE; TERPENOID DERIVATIVE; UNCLASSIFIED DRUG;

EID: 79955788089     PISSN: 1934578X     EISSN: 15559475     Source Type: Journal    
DOI: 10.1177/1934578x1100600408     Document Type: Review
Times cited : (11)

References (83)
  • 2
    • 4444295178 scopus 로고    scopus 로고
    • Occurrence, biological activity and synthesis of drimane sesquiterpenoids
    • DOI 10.1039/b311170a
    • (b) Jansen BJM, de Groot Ae. (2004) Occurrence, biological activity and synthesis of drimane sesquiterpenoids. Natural Product Reports, 21, 449-477. (Pubitemid 39182703)
    • (2004) Natural Product Reports , vol.21 , Issue.4 , pp. 449-477
    • Jansen, B.J.M.1    De Groot, Ae.2
  • 3
    • 77950213037 scopus 로고    scopus 로고
    • Synthetic investigations in the field of drimane sesquiterpenoids
    • Bioactive Natural Products (Part M)
    • Vlad PF. (2006) Synthetic investigations in the field of drimane sesquiterpenoids. Studies in Natural Products Chemistry, 33, Bioactive Natural Products (Part M), 393-432.
    • (2006) Studies in Natural Products Chemistry , vol.33 , pp. 393-432
    • Vlad, P.F.1
  • 4
    • 0345430038 scopus 로고
    • Estudio químico de la corteza del árbol Drimys winteri Forst
    • (a) Appel HH. (1948) Estudio químico de la corteza del árbol Drimys winteri Forst. Scientia (Chile), 15, 31-32;
    • (1948) Scientia (Chile) , vol.15 , pp. 31-32
    • Appel, H.H.1
  • 5
    • 37049047007 scopus 로고
    • The constitution and stereochemistry of drimenol, a novel bicyclic sesquiterpenoid
    • (b) Appel HH, Brooks CJW, Overton KH. (1959) The constitution and stereochemistry of drimenol, a novel bicyclic sesquiterpenoid. Journal of Chemical Society, 3322-3332;
    • (1959) Journal of Chemical Society , pp. 3322-3332
    • Appel, H.H.1    Brooks, C.J.W.2    Overton, K.H.3
  • 6
    • 37049040120 scopus 로고
    • 906. Sesquiterpenoids. Part II. The constitution ans stereochemistry of drimenin, isodrimenin, and confertifolin
    • (c) Appel HH, Connolly JD, Overton KH, Bond RPM. (1960) 906. Sesquiterpenoids. Part II. The constitution ans stereochemistry of drimenin, isodrimenin, and confertifolin. Journal of the Chemical Society, 4685-4692;
    • (1960) Journal of the Chemical Society , pp. 4685-4692
    • Appel, H.H.1    Connolly, J.D.2    Overton, K.H.3    Bond, R.P.M.4
  • 7
    • 28444453913 scopus 로고
    • Sesquiterpenoids III: The constitution and stereochemistry of valdiviolide, winterin and futronolide
    • Overton KH, Appel HH, Bond RPM. (1963) Sesquiterpenoids III: The constitution and stereochemistry of valdiviolide, winterin and futronolide. Tetrahedron, 19, 635-641.
    • (1963) Tetrahedron , vol.19 , pp. 635-641
    • Overton, K.H.1    Appel, H.H.2    Bond, R.P.M.3
  • 13
    • 0033694624 scopus 로고    scopus 로고
    • Synthesis of drimanes from (+)-larixol
    • Lagnel BMF, Morin C, de Groot Ae. (2000) Synthesis of drimanes from (+)-larixol. Synthesis, 13, 1907-1916.
    • (2000) Synthesis , vol.13 , pp. 1907-1916
    • Lagnel, B.M.F.1    Morin, C.2    De Groot, Ae.3
  • 14
    • 0001705942 scopus 로고
    • Naturally occurring terpenes. Synthesis of (+)- and (±)-14,15- bisnor-8α- hydroxylabd-11(E)-en-13-one, (+)-drimane-8,11-diol, and (-)-drimenol
    • Pelletier SW, Lajsic S, Ohtsuka Y, Djarmati Z. (1975) Naturally occurring terpenes. Synthesis of (+)- and (±)-14,15-bisnor-8α- hydroxylabd-11(E)-en-13-one, (+)-drimane-8,11-diol, and (-)-drimenol. Journal of Organic Chemistry, 11, 1607-1609.
    • (1975) Journal of Organic Chemistry , vol.11 , pp. 1607-1609
    • Pelletier, S.W.1    Lajsic, S.2    Ohtsuka, Y.3    Djarmati, Z.4
  • 15
    • 84971048491 scopus 로고
    • Zur Kenntnis der diterpene. 62. Mitteilung. Über eine neue, ergiebige partial synthese des ambreinolids
    • Schenk HR, Gutmann H, Jeger O, Ruzicka L. (1952) Zur Kenntnis der diterpene. 62. Mitteilung. Über eine neue, ergiebige partial synthese des ambreinolids. Helvetica Chimica Acta, 35, 817-824.
    • (1952) Helvetica Chimica Acta , vol.35 , pp. 817-824
    • Schenk, H.R.1    Gutmann, H.2    Jeger, O.3    Ruzicka, L.4
  • 16
    • 0004805433 scopus 로고
    • Chemistry of the Podocarpaceae. XXXIV. Some oxidation products of (13R)-labda- 8(17),14-dien-13-ol (manool)
    • Cambie RC, Joblin KN, Preston AF. (1971) Chemistry of the Podocarpaceae. XXXIV. Some oxidation products of (13R)-labda- 8(17),14-dien-13-ol (manool). Australian Journal of Chemistry, 24, 2365-2377.
    • (1971) Australian Journal of Chemistry , vol.24 , pp. 2365-2377
    • Cambie, R.C.1    Joblin, K.N.2    Preston, A.F.3
  • 17
    • 30144434903 scopus 로고
    • Zur kenntnis der sesquiterpene und azulene. 102. Mitteilung. Über α-, β-und allobicyclofarnesylsäure
    • (a) Caliezi A, Schinz H. (1952) Zur kenntnis der sesquiterpene und azulene. 102. Mitteilung. Über α-, β-und allobicyclofarnesylsäure. Helvetica Chimica Acta, 35, 1637-1649;
    • (1952) Helvetica Chimica Acta , vol.35 , pp. 1637-1649
    • Caliezi, A.1    Schinz, H.2
  • 18
    • 0001435114 scopus 로고
    • Untersuchungen über den sterischen verlauf säurekatalysierter cyclisationen bei terpenoiden polyenverbindungen. 3. Mitteilung. Zur stereochemie der bicyclofarnesylsäuren
    • (b) Stadler PA, Eschenmoser A, Schinz H, Stork G. (1957) Untersuchungen über den sterischen verlauf säurekatalysierter cyclisationen bei terpenoiden polyenverbindungen. 3. Mitteilung. Zur stereochemie der bicyclofarnesylsäuren. Helvetica Chimica Acta, 40, 2191-2198;
    • (1957) Helvetica Chimica Acta , vol.40 , pp. 2191-2198
    • Stadler, P.A.1    Eschenmoser, A.2    Schinz, H.3    Stork, G.4
  • 20
    • 0242696887 scopus 로고
    • The direct brominative cyclization of methyl farnesate
    • (d) Van Tamelen EE, Hessler EJ. (1966) The direct brominative cyclization of methyl farnesate. Chemical Communications, 411-413.
    • (1966) Chemical Communications , pp. 411-413
    • Van Tamelen, E.E.1    Hessler, E.J.2
  • 22
    • 0010609978 scopus 로고
    • Diterpenoids from galeopsis angustifolia
    • (a) Rodriguez B, Savona G. (1980) Diterpenoids from galeopsis angustifolia. Phytochemistry, 19, 1805-1807;
    • (1980) Phytochemistry , vol.19 , pp. 1805-1807
    • Rodriguez, B.1    Savona, G.2
  • 25
    • 0030769755 scopus 로고    scopus 로고
    • A short efficient synthesis of 11-monoacetate of drimane-8α,11-diol from norambreinolide
    • (b) Kuchkova KI, Chumakov YM, Simonov YA, Bocelli G, Panasenko AA, Vlad PF. (1997) A short efficient synthesis of 11-monoacetate of drimane-8α,11- diol from norambreinolide. Synthesis, 1045-1048. (Pubitemid 27423718)
    • (1997) Synthesis , Issue.9 , pp. 1045-1048
    • Kuchkova, K.I.1    Chumakov, Y.M.2    Simonov, Y.A.3    Bocelli, G.4    Panasenko, A.A.5    Vlad, P.F.6
  • 26
    • 0030713075 scopus 로고    scopus 로고
    • Total synthesis of both enantiomers of 15-Oxopuupehenol methylendioxy derivatives
    • DOI 10.1016/S0040-4039(97)01683-3, PII S0040403997016833
    • Arjona O, Garranzo M, Mahugo J, Maroto E, Plumet J, Saez B. (1997) Total synthesis of both enantiomers of 15-Oxopuupehenol methylendioxy derivatives. Tetrahedron Letters, 38, 7249-7252. (Pubitemid 27454228)
    • (1997) Tetrahedron Letters , vol.38 , Issue.41 , pp. 7249-7252
    • Arjona, O.1    Garranzo, M.2    Mahugo, J.3    Maroto, E.4    Plumet, J.5    Saez, B.6
  • 28
    • 0027953196 scopus 로고
    • Studies on forskolin ring C forming reactions
    • DOI 10.1016/S0040-4020(01)80741-9
    • Jordine G, Bick S, Möller U, Welzel P. (1994) Studies on forskolin ring C forming reactions. Tetrahedron, 50, 139-160. (Pubitemid 24059812)
    • (1994) Tetrahedron , vol.50 , Issue.1 , pp. 139-160
    • Jordine, G.1    Bick, S.2    Moller, U.3    Welzel, P.4    Daucher, B.5    Maas, G.6
  • 30
    • 4444371349 scopus 로고
    • Asymmetric induction studies in the synthesis of bicyclic sesquiterpenes: Attempted synthesis of (-)-drimenol
    • Lee E, Cho JH. (1989) Asymmetric induction studies in the synthesis of bicyclic sesquiterpenes: attempted synthesis of (-)-drimenol. Bulletin of the Korean Chemical Society, 10, 323-324.
    • (1989) Bulletin of the Korean Chemical Society , vol.10 , pp. 323-324
    • Lee, E.1    Cho, J.H.2
  • 31
    • 0034615857 scopus 로고    scopus 로고
    • A convenient synthesis of (+)-albicanol based on enzymatic function: Total synthesis of (+)-albicanyl acetate, (-)-albicanyl 3,4-dihydroxycinnamate, (-)-drimenol, (-)-drimenin and (-)-ambrox
    • Akita H, Nozawa M, Mitsuda A, Ohsawa H. (2000) A convenient synthesis of (+)-albicanol based on enzymatic function: total synthesis of (+)-albicanyl acetate, (-)-albicanyl 3,4-dihydroxycinnamate, (-)-drimenol, (-)-drimenin and (-)-ambrox. Tetrahedron Asymmetry, 11, 1375-1388.
    • (2000) Tetrahedron Asymmetry , vol.11 , pp. 1375-1388
    • Akita, H.1    Nozawa, M.2    Mitsuda, A.3    Ohsawa, H.4
  • 33
    • 0016187293 scopus 로고
    • Tobacco chemistry. 25. Two new drimane sesquiterpene alcohols from Greek Nicotiana tabacum L
    • (a) Hlubucek JR, Aasen AJ, Almqvist SO, Enzell CE. (1974) Tobacco chemistry. 25. Two new drimane sesquiterpene alcohols from Greek Nicotiana tabacum L. Acta Chemica Scandinavica B, 28, 289-294;
    • (1974) Acta Chemica Scandinavica B , vol.28 , pp. 289-294
    • Hlubucek, J.R.1    Aasen, A.J.2    Almqvist, S.O.3    Enzell, C.E.4
  • 34
    • 0001708116 scopus 로고
    • Tobacco Chemistry. 28. Structure and synthesis of drim-8-en-7-one, a new tobacco constituent
    • (b) Aasen AJ, Vogt CHG, Enzell CE. (1975) Tobacco Chemistry. 28. Structure and synthesis of drim-8-en-7-one, a new tobacco constituent. Acta Chemica Scandinavica B, 29, 51-55.
    • (1975) Acta Chemica Scandinavica B , vol.29 , pp. 51-55
    • Aasen, A.J.1    Vogt, C.H.G.2    Enzell, C.E.3
  • 35
    • 33645259941 scopus 로고
    • Crystal structure and absolute configuration of a new sesquiterpenoid metabolite of Fomes annosus 7α,8β,11-trihydroxydrimane
    • Donnelly DMX, O' Reilly J. (1980) Crystal structure and absolute configuration of a new sesquiterpenoid metabolite of Fomes annosus 7α,8β,11-trihydroxydrimane. Journal of Chemical Society. Perkin Transaction I, 2196-2199.
    • (1980) Journal of Chemical Society. Perkin Transaction I , pp. 2196-2199
    • Donnelly, D.M.X.1    O'Reilly, J.2
  • 39
    • 4143095276 scopus 로고
    • Alternative and stereoselective synthesis of 8β(H)-drimane, a bicyclic sesquiterpene of widespread occurrence in petroleums
    • González-Sierra M, Laborde M, Ruveda EA. (1987) Alternative and stereoselective synthesis of 8β(H)-drimane, a bicyclic sesquiterpene of widespread occurrence in petroleums. Synthetic Communications, 17, 431-441.
    • (1987) Synthetic Communications , vol.17 , pp. 431-441
    • González-Sierra, M.1    Laborde, M.2    Ruveda, E.A.3
  • 43
    • 0002425754 scopus 로고
    • Bis (p-methoxyphenyl) selenoxide as a cooxidant for selenium dioxide oxidation of benzyl alcohols
    • Ogura F, Otsubo T, Ariyoshi K, Yamaguchi H. (1983) Bis (p-methoxyphenyl) selenoxide as a cooxidant for selenium dioxide oxidation of benzyl alcohols. Chemistry Letters, 1833-1834.
    • (1983) Chemistry Letters , pp. 1833-1834
    • Ogura, F.1    Otsubo, T.2    Ariyoshi, K.3    Yamaguchi, H.4
  • 45
    • 0007049780 scopus 로고
    • Synthesis of (-)-Drim-7-ene-9α,11,1-triol. The direct precursor of (-)-warburganal
    • Oyarzún ML, Cortés M, Sierra J. (1982) Synthesis of (-)-Drim-7-ene-9α,11,1-triol. The direct precursor of (-)-warburganal. Synthetic Communications, 12, 951-958.
    • (1982) Synthetic Communications , vol.12 , pp. 951-958
    • Oyarzún, M.L.1    Cortés, M.2    Sierra, J.3
  • 46
    • 0019822053 scopus 로고
    • Synthesis of (±)-warburganal
    • Ley SV, Mahon M. (1981) Synthesis of (±)-warburganal. Tetrahedron Letters, 22, 3909-3912.
    • (1981) Tetrahedron Letters , vol.22 , pp. 3909-3912
    • Ley, S.V.1    Mahon, M.2
  • 47
    • 0029881582 scopus 로고    scopus 로고
    • A revision of the absolute configuration of drim-9(11)-en-8α-ol
    • Armstrong V, Cortés M, López J. (1996) A revision of the absolute configuration of drim-9(11)-en-8α-ol. Natural Product Letters, 8, 225-229.
    • (1996) Natural Product Letters , vol.8 , pp. 225-229
    • Armstrong, V.1    Cortés, M.2    López, J.3
  • 53
    • 82955164204 scopus 로고
    • Odeurs et Constitution III. Les substances bicyclohomofarnésiques
    • Stoll M, Hinder M. (1950) Odeurs et Constitution III. Les substances bicyclohomofarnésiques. Helvetica Chimica Acta, 33, 1251-1260.
    • (1950) Helvetica Chimica Acta , vol.33 , pp. 1251-1260
    • Stoll, M.1    Hinder, M.2
  • 54
    • 84971074349 scopus 로고
    • Chemistry of the podocarpaceae. XLIII. Utilization of 8α,13-epoxylabd-14-ene and related compounds for the preparation of ambergris-type compounds
    • (a) Cambie R, Joblin KN, Preston AF. (1972) Chemistry of the podocarpaceae. XLIII. Utilization of 8α,13-epoxylabd-14-ene and related compounds for the preparation of ambergris-type compounds. Australian Journal of Chemistry, 25, 1767-1778;
    • (1972) Australian Journal of Chemistry , vol.25 , pp. 1767-1778
    • Cambie, R.1    Joblin, K.N.2    Preston, A.F.3
  • 55
    • 84970557863 scopus 로고
    • Chemistry of the podocarpaceae. LVII. The preparation of some 1,3-dioxans with ambergris-type odours
    • (b) Cambie RC, Palmer BD. (1981) Chemistry of the podocarpaceae. LVII. The preparation of some 1,3-dioxans with ambergris-type odours. Australian Journal of Chemistry, 34, 1265-1284.
    • (1981) Australian Journal of Chemistry , vol.34 , pp. 1265-1284
    • Cambie, R.C.1    Palmer, B.D.2
  • 56
    • 49549130554 scopus 로고
    • 4 oxidation of olefins to cis-1,2-glycols using tertiary amine oxides as the oxidant
    • 4 oxidation of olefins to cis-1,2-glycols using tertiary amine oxides as the oxidant. Tetrahedron Letters, 17, 1973-1976.
    • (1976) Tetrahedron Letters , vol.17 , pp. 1973-1976
    • Van Rheenen, V.1    Kelly, R.C.2    Cha, D.Y.3
  • 58
    • 0000495151 scopus 로고
    • Reduction of steroid ketones and other carbonyl compounds by modified Wolff-Kishner method
    • Huang-Minlon. (1949) Reduction of steroid ketones and other carbonyl compounds by modified Wolff-Kishner method. Journal of the American Chemical Society, 71, 3301-3303.
    • (1949) Journal of the American Chemical Society , vol.71 , pp. 3301-3303
    • Huang-Minlon1
  • 60
    • 0023850013 scopus 로고
    • Synthesis of ambergris fragrance chemicals from sclareol, involving palladium catalysed key steps
    • DOI 10.1016/0040-4039(88)85323-1
    • Coste-Maniere I, Zahra J, Waegell B. (1988) Synthesis of ambergris fragrance chemicals from sclareol, involving palladium catalysed key steps. Tetrahedron Letters, 29, 1017-1020. (Pubitemid 18062679)
    • (1988) Tetrahedron Letters , vol.29 , Issue.9 , pp. 1017-1020
    • Coste-Maniere, I.C.1    Zahra, J.P.2    Waegell, B.3
  • 63
    • 84986366972 scopus 로고
    • The synthesis of racemic Ambrox®
    • (a) Büchi G, Wuest H. (1989) The synthesis of racemic Ambrox®. Helvetica Chimica Acta, 72, 996-1000;
    • (1989) Helvetica Chimica Acta , vol.72 , pp. 996-1000
    • Büchi, G.1    Wuest, H.2
  • 64
    • 0001231539 scopus 로고
    • Significance of the geminal dimethyl group in the odor principle of Ambrox®
    • (b) Ohloff G, Giersch W, Pickenhagen W, Furrer A, Frei B. (1985) Significance of the geminal dimethyl group in the odor principle of Ambrox®. Helvetica Chimica Acta, 68, 2022-2029.
    • (1985) Helvetica Chimica Acta , vol.68 , pp. 2022-2029
    • Ohloff, G.1    Giersch, W.2    Pickenhagen, W.3    Furrer, A.4    Frei, B.5
  • 65
    • 0000890154 scopus 로고
    • Synthesis of (+)-tricyclohexaprenol, a possible precursor of a family of tricyclic geoterpanes, and synthesis of an isomer
    • Heissler D and Ladenburger C. (1988) Synthesis of (+)-tricyclohexaprenol, a possible precursor of a family of tricyclic geoterpanes, and synthesis of an isomer. Tetrahedron, 44, 2513-2521.
    • (1988) Tetrahedron , vol.44 , pp. 2513-2521
    • Heissler, D.1    Ladenburger, C.2
  • 66
    • 51849149918 scopus 로고    scopus 로고
    • Synthesis of racemic and chiral albicanol, albicanyl acetate and cyclozonarone: Cytotoxic activity of ent-cyclozonarone
    • Delgado V, Armstrong V, Cortes M, Barrero AF. (2008) Synthesis of racemic and chiral albicanol, albicanyl acetate and cyclozonarone: cytotoxic activity of ent-cyclozonarone. Journal of Brazilian Chemical Society, 19, 1258-1263.
    • (2008) Journal of Brazilian Chemical Society , vol.19 , pp. 1258-1263
    • Delgado, V.1    Armstrong, V.2    Cortes, M.3    Barrero, A.F.4
  • 68
    • 0027738041 scopus 로고
    • Biogenetically diverse, bioactive constituents of a sponge, order Verongida: Bromotyramines and sesquiterpene-Shikimate derived metabolites
    • DOI 10.1021/jo00076a012
    • Hamann M, Scheuer P, Kelly-Borges M. (1993) Biogenetically diverse, bioactive constituents of a sponge, order Verongida: Bromotyramines and sesquiterpene-shikimate derived metabolites, Journal of Organic Chemistry, 58, 6565-6569. (Pubitemid 24011161)
    • (1993) Journal of Organic Chemistry , vol.58 , Issue.24 , pp. 6565-6569
    • Hamman, M.T.1    Scheuer, P.J.2    Kelly-Borges, M.3
  • 69
    • 0001402511 scopus 로고
    • Oxidative cleavage of hydroquinone ethers with argentic oxide
    • Snyder C, Rapoport H. (1972) Oxidative cleavage of hydroquinone ethers with argentic oxide. Journal of American Chemical Society, 94, 227-231.
    • (1972) Journal of American Chemical Society , vol.94 , pp. 227-231
    • Snyder, C.1    Rapoport, H.2
  • 70
    • 49349139162 scopus 로고
    • Structures and stereochemistry of new labdane diterpiniods from coleus forskohlii briq
    • Baht SV, Bajwa BS, Dornaver H, do Scusa N, Fehlhaber HW. (1977) Structures and stereochemistry of new labdane diterpiniods from coleus forskohlii briq. Tetrahedron letters, 18, 1669-1672.
    • (1977) Tetrahedron Letters , vol.18 , pp. 1669-1672
    • Baht, S.V.1    Bajwa, B.S.2    Dornaver, H.3    Do Scusa, N.4    Fehlhaber, H.W.5
  • 71
    • 77956185324 scopus 로고    scopus 로고
    • Asymmetric dihydroxylation of drim-7-en-11-ol: Synthesis of diasteromerically pure driman-7α;,8α,11-triol and its elaboration into novel chlorinated norlabdanic compounds
    • Vlad P, Gorincioi E, Aricu A, Barba A, Manzocchi A, Santaniello E. (2010) Asymmetric dihydroxylation of drim-7-en-11-ol: synthesis of diasteromerically pure driman-7α;,8α,11-triol and its elaboration into novel chlorinated norlabdanic compounds. Tetrahedron: Asymmetry, 21, 2108-2116.
    • (2010) Tetrahedron: Asymmetry , vol.21 , pp. 2108-2116
    • Vlad, P.1    Gorincioi, E.2    Aricu, A.3    Barba, A.4    Manzocchi, A.5    Santaniello, E.6
  • 72
    • 0013282191 scopus 로고
    • Ultrasounds in organic syntheses. 1. Effect on the formation of lithium organometallic reagents
    • Luche JL, Damiano JC. (1980) Ultrasounds in organic syntheses. 1. Effect on the formation of lithium organometallic reagents. Journal of the American Chemical Society, 102, 7926-7927.
    • (1980) Journal of the American Chemical Society , vol.102 , pp. 7926-7927
    • Luche, J.L.1    Damiano, J.C.2
  • 73
    • 0027298127 scopus 로고
    • A synthetic approach to ring B of forskolin
    • Razmilic I, López J, Cortés M. (1993) A synthetic approach to ring B of forskolin. Synthetic communications, 23, 1155-1173. (Pubitemid 23135286)
    • (1993) Synthetic Communications , vol.23 , Issue.8 , pp. 1155-1173
    • Razmilic, I.1    Lopez, J.2    Cortes, M.3
  • 75
    • 33747849809 scopus 로고
    • Compounds related to podophyllotoxin. XII. Podophyllotoxone, picropodophyllone and dehydropodophyllotoxin
    • Gensler WJ, Johnson F, Soloan ADB. (1960) Compounds related to podophyllotoxin. XII. Podophyllotoxone, picropodophyllone and dehydropodophyllotoxin. Journal of the American Chemical Society, 82, 6074-6081.
    • (1960) Journal of the American Chemical Society , vol.82 , pp. 6074-6081
    • Gensler, W.J.1    Johnson, F.2    Soloan, A.D.B.3
  • 76
    • 84989478646 scopus 로고
    • Activated dimethyl sulfoxide: Useful reagents for synthesis
    • Mancuso AJ, Swern D. (1981) Activated dimethyl sulfoxide: Useful reagents for synthesis. Synthesis, 165-185.
    • (1981) Synthesis , pp. 165-185
    • Mancuso, A.J.1    Swern, D.2
  • 78
    • 0035859696 scopus 로고    scopus 로고
    • Micribiologically-assisted hemisynthesis of 1α-hydroxydrimenol
    • Aranda G, Cortés M, Maurs M, Azerad R. (2001) Micribiologically- assisted hemisynthesis of 1α-hydroxydrimenol. Tetrahedron Asymmetry, 12, 2013-2018.
    • (2001) Tetrahedron Asymmetry , vol.12 , pp. 2013-2018
    • Aranda, G.1    Cortés, M.2    Maurs, M.3    Azerad, R.4
  • 79
    • 0027256803 scopus 로고
    • Bioconversion of drimenol into 3̀-hydroxydrimanes by Aspergillus niger. Effect of culture additives
    • Ramírez HE, Cortés M, Agosín E. (1993) Bioconversion of drimenol into 3̀-hydroxydrimanes by Aspergillus niger. Effect of culture additives. Journal of Natural Products, 56, 762-764.
    • (1993) Journal of Natural Products , vol.56 , pp. 762-764
    • Ramírez, H.E.1    Cortés, M.2    Agosín, E.3
  • 80
    • 6844262872 scopus 로고
    • Hydroxygrindelane derivatives by microbial transformation
    • (a) Hoffman JJ, Jolad SD, Bates RB, Camoun FA. (1988) Hydroxygrindelane derivatives by microbial transformation. Phytochemistry, 27, 2125-2127;
    • (1988) Phytochemistry , vol.27 , pp. 2125-2127
    • Hoffman, J.J.1    Jolad, S.D.2    Bates, R.B.3    Camoun, F.A.4
  • 81
    • 0025650852 scopus 로고
    • Microbial metabolism of the diterpene sclareol: Oxidation of the A ring by Septomyxa affinis
    • (b) Kouzi SA, McChesney JD. (1990). Microbial metabolism of the diterpene sclareol: Oxidation of the A ring by Septomyxa affinis. Helvetica Chimica Acta, 73, 2157-2164;
    • (1990) Helvetica Chimica Acta , vol.73 , pp. 2157-2164
    • Kouzi, S.A.1    McChesney, J.D.2
  • 82
    • 0025940514 scopus 로고
    • Microbial transformation of diterpenes: Hydroxylation of sclareol, manool and derivatives by Mucor plumbeus
    • (c) Aranda G, El Kortbi MS, Lallemand JI, Hammoumi, Facon I, Azerad R. (1991) Microbial transformation of diterpenes: Hydroxylation of sclareol, manool and derivatives by Mucor plumbeus. Tetrahedron, 47, 8339-8350.
    • (1991) Tetrahedron , vol.47 , pp. 8339-8350
    • Aranda, G.1    El Kortbi, M.S.2    Lallemand, J.I.3    Hammoumi Facon, I.4    Azerad, R.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.