메뉴 건너뛰기




Volumn 72, Issue 6-7, 2007, Pages 475-508

Recent advances in oxasteroids chemistry

Author keywords

Biological activity; Oxasteroid

Indexed keywords

11 HETEROSTEROID DERIVATIVE; 11 OXASTEROID DERIVATIVE; 12 OXASTEROID DERIVATIVE; 15 OXASTEROID DERIVATIVE; 16 OXASTEROID DERIVATIVE; 17 ALPHA ACETOXY 6 CHLORO 2 OXAPREGNA 4,6 DIENE 3,20 DIONE 9; 17 OXASTEROID DERIVATIVE; 2 OXACHLORMADINONE ACETATE 9; 2 OXASTEROID DERIVATIVE; 3 OXASTEROID DERIVATIVE; 4 OXASTEROID DERIVATIVE; 6 OXASTEROID DERIVATIVE; 7 OXASTEROID DERIVATIVE; ANTIANDROGEN; AROMATASE; BRASSINOLIDE; BRASSINOSTEROID; DEXTRO DIHOMO OXASTEROID DERIVATIVE; DEXTRO HOMO OXASTEROID DERIVATIVE; ESTROGEN; IPRIFLAVONE; OSATERONE ACETATE; OXASTEROID DERIVATIVE; RALOXIFENE; STEROID; UNCLASSIFIED DRUG;

EID: 34248541286     PISSN: 0039128X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.steroids.2007.03.004     Document Type: Review
Times cited : (44)

References (145)
  • 1
    • 84981932204 scopus 로고
    • Approaches to total synthesis of heterocyclic steroidal systems.
    • Huisman H.O. Approaches to total synthesis of heterocyclic steroidal systems. Angew Chem Int Ed Engl 10 7 (1971) 450-459
    • (1971) Angew Chem Int Ed Engl , vol.10 , Issue.7 , pp. 450-459
    • Huisman, H.O.1
  • 3
    • 0005167465 scopus 로고
    • Aspects of the pharmacology of aminosteroids
    • Buckett W.R. Aspects of the pharmacology of aminosteroids. Adv Steroid Biochem Pharmacol 3 (1972) 39-65
    • (1972) Adv Steroid Biochem Pharmacol , vol.3 , pp. 39-65
    • Buckett, W.R.1
  • 4
    • 0342579712 scopus 로고
    • Recent advances in the chemistry of oxasteroids
    • Ramdas S.R., and Chaudhuri A.P. Recent advances in the chemistry of oxasteroids. J Sci Ind Res 34 10 (1975) 563-585
    • (1975) J Sci Ind Res , vol.34 , Issue.10 , pp. 563-585
    • Ramdas, S.R.1    Chaudhuri, A.P.2
  • 5
    • 33751219596 scopus 로고
    • Total synthesis of heterocyclic steroidal systems.
    • Huisman H.O. Total synthesis of heterocyclic steroidal systems. Int Rev Sci: Org Chem, Ser One 8 (1973) 235-267
    • (1973) Int Rev Sci: Org Chem, Ser One , vol.8 , pp. 235-267
    • Huisman, H.O.1
  • 6
    • 34248560390 scopus 로고
    • Chemistry and biological activity of oxasteroids
    • Ramadas S.R., and Radhakrishnan J. Chemistry and biological activity of oxasteroids. J Sci Ind Res 31 3 (1972) 145-160
    • (1972) J Sci Ind Res , vol.31 , Issue.3 , pp. 145-160
    • Ramadas, S.R.1    Radhakrishnan, J.2
  • 9
    • 0001466754 scopus 로고
    • Chlormadinone acetate, a new highly active gestation-supporting agent
    • Brennan D.M., and Kraay R.J. Chlormadinone acetate, a new highly active gestation-supporting agent. Acta Endocrinol 44 3 (1963) 367-379
    • (1963) Acta Endocrinol , vol.44 , Issue.3 , pp. 367-379
    • Brennan, D.M.1    Kraay, R.J.2
  • 10
    • 49549130554 scopus 로고
    • An improved catalytic osmium tetroxide oxidation of olefins to cis-1,2-glycols using tertiary amine oxides as the oxidant
    • Van Rheenen V., Kelly R.C., and Cha D.Y. An improved catalytic osmium tetroxide oxidation of olefins to cis-1,2-glycols using tertiary amine oxides as the oxidant. Tetrahedron Lett (1976) 1973-1976
    • (1976) Tetrahedron Lett , pp. 1973-1976
    • Van Rheenen, V.1    Kelly, R.C.2    Cha, D.Y.3
  • 12
    • 0015424347 scopus 로고
    • Antiandrogens. 2′,3′α-Tetrahydrofuran-2′-spiro-17-(1,2α-methylene-4-androsten-3-ones)
    • Rasmusson G.H., Chen A., Reynolds G.F., Patanelli D.J., Patchett A.A., and Arth G.E. Antiandrogens. 2′,3′α-Tetrahydrofuran-2′-spiro-17-(1,2α-methylene-4-androsten-3-ones). J Med Chem 15 11 (1972) 1165-1168
    • (1972) J Med Chem , vol.15 , Issue.11 , pp. 1165-1168
    • Rasmusson, G.H.1    Chen, A.2    Reynolds, G.F.3    Patanelli, D.J.4    Patchett, A.A.5    Arth, G.E.6
  • 13
    • 0000084418 scopus 로고
    • Steroidal aldosterone blockers
    • Cella John A., and Tweit R.C. Steroidal aldosterone blockers. J Org Chem 24 (1959) 1109-1110
    • (1959) J Org Chem , vol.24 , pp. 1109-1110
    • Cella John, A.1    Tweit, R.C.2
  • 14
    • 0039292624 scopus 로고    scopus 로고
    • Expeditious synthetic route to B-ring functionalized 2-oxa-steroids: synthesis of 17-ethylenedioxy-6α-hydroxy-2-oxa-4-androsten-3-one as key synthon
    • Nangia A., and Anthony A. Expeditious synthetic route to B-ring functionalized 2-oxa-steroids: synthesis of 17-ethylenedioxy-6α-hydroxy-2-oxa-4-androsten-3-one as key synthon. Indian J Chem, Sect B 36B 12 (1997) 1113-1118
    • (1997) Indian J Chem, Sect B , vol.36 B , Issue.12 , pp. 1113-1118
    • Nangia, A.1    Anthony, A.2
  • 15
    • 0035213409 scopus 로고    scopus 로고
    • Steroidal aromatase inhibitors: model receptor surfaces and 3D QSAR
    • Jetti Ram K.R., Anthony A., Nangia A., and Desiraju G.R. Steroidal aromatase inhibitors: model receptor surfaces and 3D QSAR. Indian J Chem, Sect B 40B 11 (2001) 1054-1062
    • (2001) Indian J Chem, Sect B , vol.40 B , Issue.11 , pp. 1054-1062
    • Jetti Ram, K.R.1    Anthony, A.2    Nangia, A.3    Desiraju, G.R.4
  • 16
    • 0041038159 scopus 로고
    • Functionalized enamines. Annulation of enamines of polycyclic α,β-unsaturated ketones. Facile partial synthesis of furano, indolo and benzo steroids. Total synthesis of 3-oxa-A-norsteroid
    • Manhas M.S., Brown J.W., Pandit U.K., and Houdewind P. Functionalized enamines. Annulation of enamines of polycyclic α,β-unsaturated ketones. Facile partial synthesis of furano, indolo and benzo steroids. Total synthesis of 3-oxa-A-norsteroid. Tetrahedron 31 10 (1975) 1325-1330
    • (1975) Tetrahedron , vol.31 , Issue.10 , pp. 1325-1330
    • Manhas, M.S.1    Brown, J.W.2    Pandit, U.K.3    Houdewind, P.4
  • 17
    • 34248505372 scopus 로고
    • Functionalized enamines. Synthesis of fused furan systems via reaction of conjugated enamines with α-haloketones
    • Pandit U.K., Reus H.R., and De Jonge M.K. Functionalized enamines. Synthesis of fused furan systems via reaction of conjugated enamines with α-haloketones. Recueil des Travaux Chimiques des Pays-Bas 89 9 (1970) 956-960
    • (1970) Recueil des Travaux Chimiques des Pays-Bas , vol.89 , Issue.9 , pp. 956-960
    • Pandit, U.K.1    Reus, H.R.2    De Jonge, M.K.3
  • 18
    • 0014443872 scopus 로고
    • Total synthesis of some (±)-18-methyl-9β,10α-androstanes and (±)-18-methyl-9β,10α-D-homoandrostanes
    • Gardner J.N., Anderson B.A., and Oliveto E.P. Total synthesis of some (±)-18-methyl-9β,10α-androstanes and (±)-18-methyl-9β,10α-D-homoandrostanes. J Org Chem 34 1 (1969) 107-112
    • (1969) J Org Chem , vol.34 , Issue.1 , pp. 107-112
    • Gardner, J.N.1    Anderson, B.A.2    Oliveto, E.P.3
  • 19
    • 33947299508 scopus 로고
    • Synthesis of an A-furano steroid
    • Lednicer D., and Emmert D.E. Synthesis of an A-furano steroid. J Org Chem 34 4 (1969) 1151-1154
    • (1969) J Org Chem , vol.34 , Issue.4 , pp. 1151-1154
    • Lednicer, D.1    Emmert, D.E.2
  • 20
    • 34248521374 scopus 로고
    • Total synthesis of 7-methyl-2-phenyl-3-oxa-A-nor-14-isoestra-1,5(10),6,8-tetraen-17α-ol
    • Ramadas S.R., and Padmanabhan S. Total synthesis of 7-methyl-2-phenyl-3-oxa-A-nor-14-isoestra-1,5(10),6,8-tetraen-17α-ol. Indian J Chem, Sect B 16B 5 (1978) 418-419
    • (1978) Indian J Chem, Sect B , vol.16 B , Issue.5 , pp. 418-419
    • Ramadas, S.R.1    Padmanabhan, S.2
  • 21
    • 0018774298 scopus 로고
    • Heterocyclic steroids. Studies on the total synthesis of racemic 2-phenyl-7-methyl-3-oxa-A-nor-14β-estra-1,5(10),6,8-tetraen-17α-ol
    • Ramadas S.R., and Padmanabhan S. Heterocyclic steroids. Studies on the total synthesis of racemic 2-phenyl-7-methyl-3-oxa-A-nor-14β-estra-1,5(10),6,8-tetraen-17α-ol. Steroids 33 2 (1979) 153-166
    • (1979) Steroids , vol.33 , Issue.2 , pp. 153-166
    • Ramadas, S.R.1    Padmanabhan, S.2
  • 22
    • 34248526457 scopus 로고
    • Dihydric alcohols obtained by the reduction of substituted dihydroresorcinols
    • Crossley A.W., and Renouf N. Dihydric alcohols obtained by the reduction of substituted dihydroresorcinols. J Chem Soc Trans 107 (1915) 602-610
    • (1915) J Chem Soc Trans , vol.107 , pp. 602-610
    • Crossley, A.W.1    Renouf, N.2
  • 24
    • 0014322484 scopus 로고
    • Synthesis of estrone via novel intermediates. Mechanism of the coupling reaction of vinyl carbinol with a β-diketone
    • Kuo C.H., Taub D., and Wendler N.L. Synthesis of estrone via novel intermediates. Mechanism of the coupling reaction of vinyl carbinol with a β-diketone. J Org Chem 33 8 (1968) 3126-3132
    • (1968) J Org Chem , vol.33 , Issue.8 , pp. 3126-3132
    • Kuo, C.H.1    Taub, D.2    Wendler, N.L.3
  • 25
    • 0019440436 scopus 로고
    • Totally synthetic steroid heterocycles. Synthesis of racemic A-nor-3,16-dithia- and 2-methyl-A-nor-3-oxa-16-thia-D-homo-1,5(10),8,14-estra-tetraen-17a-ols
    • Terasawa T., and Okada T. Totally synthetic steroid heterocycles. Synthesis of racemic A-nor-3,16-dithia- and 2-methyl-A-nor-3-oxa-16-thia-D-homo-1,5(10),8,14-estra-tetraen-17a-ols. Steroids 37 4 (1981) 445-453
    • (1981) Steroids , vol.37 , Issue.4 , pp. 445-453
    • Terasawa, T.1    Okada, T.2
  • 27
    • 33845378483 scopus 로고
    • Photoinduced transformations. A four-step substitution of a carbonyl group of steroidal ketones by an oxygen atom. A new method for the synthesis of cyclic ethers
    • Suginome H., and Yamada S. Photoinduced transformations. A four-step substitution of a carbonyl group of steroidal ketones by an oxygen atom. A new method for the synthesis of cyclic ethers. J Org Chem 50 14 (1985) 2489-2494
    • (1985) J Org Chem , vol.50 , Issue.14 , pp. 2489-2494
    • Suginome, H.1    Yamada, S.2
  • 28
    • 0001643160 scopus 로고
    • Photoinduced transformations. Transformations of five- (and six-) membered cyclic alcohols into five- (and six-) membered cyclic ethers-a new method of a two-step transformation of hydroxy steroids into oxasteroids
    • Suginome H., and Yamada S. Photoinduced transformations. Transformations of five- (and six-) membered cyclic alcohols into five- (and six-) membered cyclic ethers-a new method of a two-step transformation of hydroxy steroids into oxasteroids. J Org Chem 49 20 (1984) 3753-3762
    • (1984) J Org Chem , vol.49 , Issue.20 , pp. 3753-3762
    • Suginome, H.1    Yamada, S.2
  • 29
    • 34248556812 scopus 로고
    • Photoinduced molecular transformations. Reactions of alkoxyl radicals generated from hypoiodites of 3β-hydroxy-7-oxo-Δ 5-steroids. Synthesis of some functionalized oxasteroids
    • Suginome H., and Kondoh T. Photoinduced molecular transformations. Reactions of alkoxyl radicals generated from hypoiodites of 3β-hydroxy-7-oxo-Δ 5-steroids. Synthesis of some functionalized oxasteroids. J Chem Soc, Perkin Trans 1: Org Bio-Org Chem 22 (1992) 3119-3124
    • (1992) J Chem Soc, Perkin Trans 1: Org Bio-Org Chem , vol.22 , pp. 3119-3124
    • Suginome, H.1    Kondoh, T.2
  • 30
    • 34248544118 scopus 로고    scopus 로고
    • Bakshi RK, Patel GF, Rasmusson GH, Tolman RL. Synthesis of 4-oxa and 4-thia steroids as 5α-reductase inhibitors. USXXAM US 5,777,134; 1998. p. 23.
  • 31
    • 0019144989 scopus 로고
    • Total synthesis of 3,17β-dihydroxy-6-oxaestra-1,3,5(10),7-tetraene and related miroestrol analogs
    • Findlay J.A., Mebe P., Stern M.D., and Givner M.L. Total synthesis of 3,17β-dihydroxy-6-oxaestra-1,3,5(10),7-tetraene and related miroestrol analogs. Can J Chem 58 14 (1980) 1427-1434
    • (1980) Can J Chem , vol.58 , Issue.14 , pp. 1427-1434
    • Findlay, J.A.1    Mebe, P.2    Stern, M.D.3    Givner, M.L.4
  • 32
    • 0002469154 scopus 로고
    • New syntheses of estrone, dl-8-isoestrone, and dl-19-nortestosterone
    • Ananchenko S.N., and Torgov I.V. New syntheses of estrone, dl-8-isoestrone, and dl-19-nortestosterone. Tetrahedron Lett (1963) 1553-1558
    • (1963) Tetrahedron Lett , pp. 1553-1558
    • Ananchenko, S.N.1    Torgov, I.V.2
  • 33
    • 34248544117 scopus 로고
    • Synthesis of 13-aza-18-nor-7-methyl-17-oxo-6-oxa-estra-1,3,5(10), 9(11)-tetraene 3-methyl ether and 13-aza-18-nor-7-methyl-17-oxo-6-thia-estra-1,3,5(10),9(11)-tetraene 3-methyl ether
    • Trehan I.R., Farwaha R., Sharma R.K., and Kaul R.L. Synthesis of 13-aza-18-nor-7-methyl-17-oxo-6-oxa-estra-1,3,5(10), 9(11)-tetraene 3-methyl ether and 13-aza-18-nor-7-methyl-17-oxo-6-thia-estra-1,3,5(10),9(11)-tetraene 3-methyl ether. Indian J Chem, Sect B 19B 2 (1980) 87-89
    • (1980) Indian J Chem, Sect B , vol.19 B , Issue.2 , pp. 87-89
    • Trehan, I.R.1    Farwaha, R.2    Sharma, R.K.3    Kaul, R.L.4
  • 34
    • 0017649596 scopus 로고
    • Synthesis of insect antijuvenile hormones
    • Ohta T., and Bowers W.S. Synthesis of insect antijuvenile hormones. Chem Pharm Bull 25 10 (1977) 2788-2789
    • (1977) Chem Pharm Bull , vol.25 , Issue.10 , pp. 2788-2789
    • Ohta, T.1    Bowers, W.S.2
  • 35
    • 0345391556 scopus 로고
    • The utility of phosphonate carbanions in olefin synthesis
    • Wadsworth W.S., and Emmons W.D. The utility of phosphonate carbanions in olefin synthesis. J Am Chem Soc 83 (1961) 1733-1738
    • (1961) J Am Chem Soc , vol.83 , pp. 1733-1738
    • Wadsworth, W.S.1    Emmons, W.D.2
  • 36
    • 4744348912 scopus 로고
    • Stereospecific and stereoselective reactions. Preparation of amines from alcohols
    • Mitsunobu O., Wada M., and Sano T. Stereospecific and stereoselective reactions. Preparation of amines from alcohols. J Am Chem Soc 94 2 (1972) 697-807
    • (1972) J Am Chem Soc , vol.94 , Issue.2 , pp. 697-807
    • Mitsunobu, O.1    Wada, M.2    Sano, T.3
  • 37
    • 38249030367 scopus 로고
    • Heterosteroids via organoiron complexes: enantioselective synthesis of the 9-(4-keto-1-methylcyclohex-2-enyl)-8-keto-des-AB-ergosta-14,15-22,23-diene; an easy rearrangement of the title compound into a 6-oxa B-nor heterosteroid structure
    • Mincione E., Bovicelli P., Cerrini S., and Lamba D. Heterosteroids via organoiron complexes: enantioselective synthesis of the 9-(4-keto-1-methylcyclohex-2-enyl)-8-keto-des-AB-ergosta-14,15-22,23-diene; an easy rearrangement of the title compound into a 6-oxa B-nor heterosteroid structure. Heterocycles 27 3 (1988) 605-612
    • (1988) Heterocycles , vol.27 , Issue.3 , pp. 605-612
    • Mincione, E.1    Bovicelli, P.2    Cerrini, S.3    Lamba, D.4
  • 38
    • 34248538892 scopus 로고
    • Synthesis via organoiron complexes of 9-(4-keto-1-methylcyclohex-2-enyl)-8-keto-des-AB-ergost-22,23-ene; a useful chiral intermediate in steroid synthesis
    • Mincione E., Bovicelli P., Cerrini S., and Lamba D. Synthesis via organoiron complexes of 9-(4-keto-1-methylcyclohex-2-enyl)-8-keto-des-AB-ergost-22,23-ene; a useful chiral intermediate in steroid synthesis. Heterocycles 23 7 (1985) 1607-1610
    • (1985) Heterocycles , vol.23 , Issue.7 , pp. 1607-1610
    • Mincione, E.1    Bovicelli, P.2    Cerrini, S.3    Lamba, D.4
  • 39
    • 84989484020 scopus 로고
    • The facile silylation of aldehydes and ketones using trimethylsilyl iodide: an exceptionally simple procedure for the generation of thermodynamically equilibrated trimethylsilyl enol ethers
    • Miller R.D., and McKean D.R. The facile silylation of aldehydes and ketones using trimethylsilyl iodide: an exceptionally simple procedure for the generation of thermodynamically equilibrated trimethylsilyl enol ethers. Synthesis (1979) 730-732
    • (1979) Synthesis , pp. 730-732
    • Miller, R.D.1    McKean, D.R.2
  • 40
    • 0001002063 scopus 로고
    • Synthetic methods. Halogenation of carbonyl compounds via silyl enol ethers
    • Reuss R.H., and Hassner A. Synthetic methods. Halogenation of carbonyl compounds via silyl enol ethers. J Org Chem 39 12 (1974) 1785-1787
    • (1974) J Org Chem , vol.39 , Issue.12 , pp. 1785-1787
    • Reuss, R.H.1    Hassner, A.2
  • 41
    • 1542390199 scopus 로고
    • Organoiron complexes in organic synthesis. A facile TMS-mediated decarboxylation of organoiron complexes
    • Chandler M., Parsons P.J., and Mincione E. Organoiron complexes in organic synthesis. A facile TMS-mediated decarboxylation of organoiron complexes. Tetrahedron Lett 24 51 (1983) 5781-5784
    • (1983) Tetrahedron Lett , vol.24 , Issue.51 , pp. 5781-5784
    • Chandler, M.1    Parsons, P.J.2    Mincione, E.3
  • 42
    • 34248505371 scopus 로고
    • Organoiron complexes in organic synthesis. New strategies for steroid and aphidicolane synthesis
    • Pearson A.J., Heywood G.C., and Chandler M. Organoiron complexes in organic synthesis. New strategies for steroid and aphidicolane synthesis. J Chem Soc, Perkin Trans 1: Org Bio-Org Chem (1982) 2631-2639
    • (1982) J Chem Soc, Perkin Trans 1: Org Bio-Org Chem , pp. 2631-2639
    • Pearson, A.J.1    Heywood, G.C.2    Chandler, M.3
  • 43
    • 0009277812 scopus 로고
    • Inter- and intramolecular hetero-Diels-Alder reactions. Synthesis of enantiomerically pure heterosteroids by intramolecular hetero-Diels-Alder reaction
    • Tietze L.F., Beifuss U., Loekoes M., Rischer M., Sheldrick G.M., and Goehrt A. Inter- and intramolecular hetero-Diels-Alder reactions. Synthesis of enantiomerically pure heterosteroids by intramolecular hetero-Diels-Alder reaction. Angew Chem 102 5 (1990) 545-547
    • (1990) Angew Chem , vol.102 , Issue.5 , pp. 545-547
    • Tietze, L.F.1    Beifuss, U.2    Loekoes, M.3    Rischer, M.4    Sheldrick, G.M.5    Goehrt, A.6
  • 44
    • 33750818819 scopus 로고
    • Synthesis of oxasteroidal skeletons by (4+2) type cycloaddition of coumarin and 6-methyl-2-pyrone with siloxydienes mediated by tert-butyldimethylsilyl triflate
    • Lee Y.G., Utsumi Y., Ohkata K., and Akiba K. Synthesis of oxasteroidal skeletons by (4+2) type cycloaddition of coumarin and 6-methyl-2-pyrone with siloxydienes mediated by tert-butyldimethylsilyl triflate. Heterocycles 30 2 (1990) 813-816
    • (1990) Heterocycles , vol.30 , Issue.2 , pp. 813-816
    • Lee, Y.G.1    Utsumi, Y.2    Ohkata, K.3    Akiba, K.4
  • 45
    • 0025879870 scopus 로고
    • Synthesis of new pentacyclic heterocyclic steroidal analogs, 6-oxabenz[3,4]-D-homoestra-1,3,5(10),8,14-pentaen-17a-one and 3a,4,5,13-tetrahydro-3H-[2]benzothieno[5,4-d]naphtho[1,2-b]pyran
    • Babu B.R., Ramana D.V., and Ramadas S.R. Synthesis of new pentacyclic heterocyclic steroidal analogs, 6-oxabenz[3,4]-D-homoestra-1,3,5(10),8,14-pentaen-17a-one and 3a,4,5,13-tetrahydro-3H-[2]benzothieno[5,4-d]naphtho[1,2-b]pyran. Steroids 56 7 (1991) 388-391
    • (1991) Steroids , vol.56 , Issue.7 , pp. 388-391
    • Babu, B.R.1    Ramana, D.V.2    Ramadas, S.R.3
  • 46
    • 33645285804 scopus 로고
    • Synthesis of some novel heterocyclics from 2,3-dihydro-4H-naphtho[1,2-b]pyran-4-one
    • Sharma S.D., and Kaur S. Synthesis of some novel heterocyclics from 2,3-dihydro-4H-naphtho[1,2-b]pyran-4-one. Indian J Chem, Sect B 23B 6 (1984) 518-521
    • (1984) Indian J Chem, Sect B , vol.23 B , Issue.6 , pp. 518-521
    • Sharma, S.D.1    Kaur, S.2
  • 47
    • 0002224197 scopus 로고
    • The synthesis of 8-hydroxy-1-oxo-4-methyl-1,2,3,5,6,7-hexahydronaphthalene
    • Newman M.S., and Mekler A.B. The synthesis of 8-hydroxy-1-oxo-4-methyl-1,2,3,5,6,7-hexahydronaphthalene. J Am Chem Soc 82 (1960) 4039-4041
    • (1960) J Am Chem Soc , vol.82 , pp. 4039-4041
    • Newman, M.S.1    Mekler, A.B.2
  • 49
    • 34248541768 scopus 로고
    • Mercuric oxide-iodine oxidation of 6β-hydroxypregnanes. Influence of the C-5 functionality
    • Brachet-Cota A.L., and Burton G. Mercuric oxide-iodine oxidation of 6β-hydroxypregnanes. Influence of the C-5 functionality. Z Naturforsch, B: Chem Sci 43 4 (1988) 491-495
    • (1988) Z Naturforsch, B: Chem Sci , vol.43 , Issue.4 , pp. 491-495
    • Brachet-Cota, A.L.1    Burton, G.2
  • 50
    • 0032253412 scopus 로고    scopus 로고
    • Synthesis of oxa-steroidal-estrogen analogues
    • Zou Y., Weng L.L., and Zheng H. Synthesis of oxa-steroidal-estrogen analogues. Chin Chem Lett 9 3 (1998) 249-250
    • (1998) Chin Chem Lett , vol.9 , Issue.3 , pp. 249-250
    • Zou, Y.1    Weng, L.L.2    Zheng, H.3
  • 51
    • 0013774153 scopus 로고
    • Total synthesis of derivatives of (+)-oxa and aza-estrone
    • Smith H., Douglas G.H., and Walk C.R. Total synthesis of derivatives of (+)-oxa and aza-estrone. Experientia 20 8 (1964) 418-419
    • (1964) Experientia , vol.20 , Issue.8 , pp. 418-419
    • Smith, H.1    Douglas, G.H.2    Walk, C.R.3
  • 52
    • 0002679783 scopus 로고
    • Totally synthetic steroid hormones. 13β-Alkylgona-1,3,5(10)-trienes, 13β-alkylgon-4-en-3-ones, and related compounds
    • Smith H. Totally synthetic steroid hormones. 13β-Alkylgona-1,3,5(10)-trienes, 13β-alkylgon-4-en-3-ones, and related compounds. J Chem Soc (1964) 4472-4492
    • (1964) J Chem Soc , pp. 4472-4492
    • Smith, H.1
  • 53
    • 0019200255 scopus 로고
    • A one step transformation of a 7-oxo steroid into a 7-oxa steroid. A new photo-oxidation of cyclic ketone
    • Suginome H., and Shea C.M. A one step transformation of a 7-oxo steroid into a 7-oxa steroid. A new photo-oxidation of cyclic ketone. Bull Chem Soc Jpn 53 11 (1980) 3387-3388
    • (1980) Bull Chem Soc Jpn , vol.53 , Issue.11 , pp. 3387-3388
    • Suginome, H.1    Shea, C.M.2
  • 54
    • 0015851660 scopus 로고
    • Steroids. Reactions of steroidal β-oxo cyclopropanes with Jacques reagent
    • Cerny V. Steroids. Reactions of steroidal β-oxo cyclopropanes with Jacques reagent. Collect Czech Chem Commun 38 5 (1973) 1563-1570
    • (1973) Collect Czech Chem Commun , vol.38 , Issue.5 , pp. 1563-1570
    • Cerny, V.1
  • 55
    • 34248560389 scopus 로고
    • Photo-induced transformations. The photo-Beckmann rearrangement of 3α,5-cyclo-5α-cholestan-7-one oxime, a βγ-cyclopropyl ketone oxime
    • Suginome H., and Shea C.M. Photo-induced transformations. The photo-Beckmann rearrangement of 3α,5-cyclo-5α-cholestan-7-one oxime, a βγ-cyclopropyl ketone oxime. J Chem Soc, Perkin Trans 1: Org Bio-Org Chem (1980) 2268-2271
    • (1980) J Chem Soc, Perkin Trans 1: Org Bio-Org Chem , pp. 2268-2271
    • Suginome, H.1    Shea, C.M.2
  • 56
    • 84954977094 scopus 로고
    • Short-step synthesis of homodolicholide
    • Sakakibara M., and Mori K. Short-step synthesis of homodolicholide. Agric Biol Chem 47 6 (1983) 1407-1408
    • (1983) Agric Biol Chem , vol.47 , Issue.6 , pp. 1407-1408
    • Sakakibara, M.1    Mori, K.2
  • 57
    • 33750473982 scopus 로고
    • Brassinolide-related bioactive sterols in Dolichos lablab: brassinolide, castasterone and a new analog, homodolicholide
    • Yokota T., Baba J., and Takahashi N. Brassinolide-related bioactive sterols in Dolichos lablab: brassinolide, castasterone and a new analog, homodolicholide. Agric Biol Chem 47 6 (1983) 1409-1411
    • (1983) Agric Biol Chem , vol.47 , Issue.6 , pp. 1409-1411
    • Yokota, T.1    Baba, J.2    Takahashi, N.3
  • 58
    • 84954977094 scopus 로고
    • Short-step synthesis of homodolichosterone
    • Sakakibara M., and Mori K. Short-step synthesis of homodolichosterone. Agric Biol Chem 47 6 (1983) 1405-1406
    • (1983) Agric Biol Chem , vol.47 , Issue.6 , pp. 1405-1406
    • Sakakibara, M.1    Mori, K.2
  • 59
    • 0001315459 scopus 로고
    • Brassinolide and its analogs. Synthesis of naturally occurring brassinosteroids employing cleavage of 23,34-epoxides as key reactions. Synthesis of brassinolide, castasterone, dolicholide, dolichosterone, homodolicholide, homodolichosterone, 6-deoxocastasterone and 6-deoxodolichosterone
    • Mori K., Sakakibara M., and Okada K. Brassinolide and its analogs. Synthesis of naturally occurring brassinosteroids employing cleavage of 23,34-epoxides as key reactions. Synthesis of brassinolide, castasterone, dolicholide, dolichosterone, homodolicholide, homodolichosterone, 6-deoxocastasterone and 6-deoxodolichosterone. Tetrahedron 40 10 (1984) 1767-1781
    • (1984) Tetrahedron , vol.40 , Issue.10 , pp. 1767-1781
    • Mori, K.1    Sakakibara, M.2    Okada, K.3
  • 60
    • 0021984581 scopus 로고
    • Synthesis of (2R,3S,22R,23R)- and (2R,3S,22S,23S)-2,3,22,23-tetrahydroxy-B-homo-8-oxa-5α-ergostan-7-ones, two new brassinolide analogs
    • Anastasia M., Allevi P., Ciuffreda P., Fiecchi A., and Scala A. Synthesis of (2R,3S,22R,23R)- and (2R,3S,22S,23S)-2,3,22,23-tetrahydroxy-B-homo-8-oxa-5α-ergostan-7-ones, two new brassinolide analogs. J Org Chem 50 3 (1985) 321-325
    • (1985) J Org Chem , vol.50 , Issue.3 , pp. 321-325
    • Anastasia, M.1    Allevi, P.2    Ciuffreda, P.3    Fiecchi, A.4    Scala, A.5
  • 61
    • 23044526760 scopus 로고    scopus 로고
    • On steroids. Synthesis of (20S)-2α,3α-dihydroxy-6-oxo-7-oxa-7a-homo-5α-pregnane-20-carboxylic acid as a brassinosteroid part of ligand for binding to affinity chromatography carriers
    • Kohout L., Chodounska H., Macek T., and Strnad M. On steroids. Synthesis of (20S)-2α,3α-dihydroxy-6-oxo-7-oxa-7a-homo-5α-pregnane-20-carboxylic acid as a brassinosteroid part of ligand for binding to affinity chromatography carriers. Collect Czech Chem Commun 65 11 (2000) 1754-1761
    • (2000) Collect Czech Chem Commun , vol.65 , Issue.11 , pp. 1754-1761
    • Kohout, L.1    Chodounska, H.2    Macek, T.3    Strnad, M.4
  • 62
    • 0020510544 scopus 로고
    • Improved synthesis of brassinolide
    • Sakakibara M., and Mori K. Improved synthesis of brassinolide. Agric Biol Chem 47 3 (1983) 663-664
    • (1983) Agric Biol Chem , vol.47 , Issue.3 , pp. 663-664
    • Sakakibara, M.1    Mori, K.2
  • 63
    • 0017174984 scopus 로고
    • Steroids and related products. The synthesis of 11-oxa steroids. The synthesis of 17,21-dihydroxy-11-oxa-4-pregnene-3,20-dione, an 11-oxa analog of the 17-hydroxylated glucocorticoids
    • Salvi V.S., Mukherjee D., Chowdhury M.N.R., and Engel C.R. Steroids and related products. The synthesis of 11-oxa steroids. The synthesis of 17,21-dihydroxy-11-oxa-4-pregnene-3,20-dione, an 11-oxa analog of the 17-hydroxylated glucocorticoids. Steroids 27 5 (1976) 717-725
    • (1976) Steroids , vol.27 , Issue.5 , pp. 717-725
    • Salvi, V.S.1    Mukherjee, D.2    Chowdhury, M.N.R.3    Engel, C.R.4
  • 64
    • 0015265087 scopus 로고
    • Steroids and related products. Synthesis of 11-oxa steroids
    • Engel C.R., Rastogi R.C., and Chowdhury M.N.R. Steroids and related products. Synthesis of 11-oxa steroids. Steroids 19 1 (1972) 1-24
    • (1972) Steroids , vol.19 , Issue.1 , pp. 1-24
    • Engel, C.R.1    Rastogi, R.C.2    Chowdhury, M.N.R.3
  • 65
    • 0014259947 scopus 로고
    • Steroids and related products. The synthesis of 11-oxa steroids. 11-Oxaprogesterone
    • Engel C.R., and Chowdhury M.N.R. Steroids and related products. The synthesis of 11-oxa steroids. 11-Oxaprogesterone. Tetrahedron Lett (1968) 2107-2111
    • (1968) Tetrahedron Lett , pp. 2107-2111
    • Engel, C.R.1    Chowdhury, M.N.R.2
  • 66
    • 0016731302 scopus 로고
    • Steroids and related products. Synthesis of 11-oxa steroids. 17-Acetoxy-11-oxaprogesterone
    • Engel C.R., Salvi S., and Chowdhury M.N.R. Steroids and related products. Synthesis of 11-oxa steroids. 17-Acetoxy-11-oxaprogesterone. Steroids 25 6 (1975) 781-790
    • (1975) Steroids , vol.25 , Issue.6 , pp. 781-790
    • Engel, C.R.1    Salvi, S.2    Chowdhury, M.N.R.3
  • 67
    • 0016589523 scopus 로고
    • 11-Oxa and 17α-hydroxymethyl analogs of steroid hormones and their derivatives
    • Engel C.R., Mukherjee D., Chowdhury M.N.R., Ramani G., and Salvi V.S. 11-Oxa and 17α-hydroxymethyl analogs of steroid hormones and their derivatives. J Steroid Biochem 6 5 (1975) 585-597
    • (1975) J Steroid Biochem , vol.6 , Issue.5 , pp. 585-597
    • Engel, C.R.1    Mukherjee, D.2    Chowdhury, M.N.R.3    Ramani, G.4    Salvi, V.S.5
  • 68
    • 0014322443 scopus 로고
    • One-step procedure for the preparation of tertiary α-ketols from the corresponding ketones
    • Gardner J.N., Carlon F.E., and Gnoj O. One-step procedure for the preparation of tertiary α-ketols from the corresponding ketones. J Org Chem 33 8 (1968) 3294-3297
    • (1968) J Org Chem , vol.33 , Issue.8 , pp. 3294-3297
    • Gardner, J.N.1    Carlon, F.E.2    Gnoj, O.3
  • 69
    • 37049047158 scopus 로고
    • Oxygenation of steroid ketones in strongly basic medium: a new method of preparation of 17α-hydroxypregnan-20-ones
    • Bailey E.J., Barton D.H.R., Elks J., and Templeton J.F. Oxygenation of steroid ketones in strongly basic medium: a new method of preparation of 17α-hydroxypregnan-20-ones. J Chem Soc (1962) 1578-1591
    • (1962) J Chem Soc , pp. 1578-1591
    • Bailey, E.J.1    Barton, D.H.R.2    Elks, J.3    Templeton, J.F.4
  • 70
    • 0019833185 scopus 로고
    • One-step synthesis of 11-oxasteroid analogs from cyclic β-ketodiesters through Pechmann cyclocondensation
    • Dutt S., and Karmakar T.K. One-step synthesis of 11-oxasteroid analogs from cyclic β-ketodiesters through Pechmann cyclocondensation. Synthesis (1981) 826-828
    • (1981) Synthesis , pp. 826-828
    • Dutt, S.1    Karmakar, T.K.2
  • 71
    • 33947462803 scopus 로고
    • Dieckmann cyclization. Cyclization of triethyl pentane-1,2,5-tricarboxylate
    • Sen K., and Bagchi P. Dieckmann cyclization. Cyclization of triethyl pentane-1,2,5-tricarboxylate. J Org Chem 23 (1958) 1125-1128
    • (1958) J Org Chem , vol.23 , pp. 1125-1128
    • Sen, K.1    Bagchi, P.2
  • 72
    • 34248514243 scopus 로고
    • Heterocyclic steroids. Synthesis of some spiro derivatives of 7,8-diaza-11-oxasteroids
    • Altomare C., Carotti A., and Campagna F. Heterocyclic steroids. Synthesis of some spiro derivatives of 7,8-diaza-11-oxasteroids. J Heterocycl Chem 20 6 (1983) 1751-1752
    • (1983) J Heterocycl Chem , vol.20 , Issue.6 , pp. 1751-1752
    • Altomare, C.1    Carotti, A.2    Campagna, F.3
  • 73
    • 0019428439 scopus 로고
    • A simple route to 8-aza-11-oxasteroids and 8-aza-11-oxa-D-homosteroids
    • Carotti A. A simple route to 8-aza-11-oxasteroids and 8-aza-11-oxa-D-homosteroids. Farmaco, Edizione Sci 36 2 (1981) 146-151
    • (1981) Farmaco, Edizione Sci , vol.36 , Issue.2 , pp. 146-151
    • Carotti, A.1
  • 74
    • 0021839331 scopus 로고
    • Unusual cyclization of 3,20-bisethylenedioxy-9,11-seco-C-nor-5α-pregnane-9β,11-diol into 11-oxa-5α,17α-pregnane-3,20-dione
    • Nagano H., Iwadare T., and Shiota M. Unusual cyclization of 3,20-bisethylenedioxy-9,11-seco-C-nor-5α-pregnane-9β,11-diol into 11-oxa-5α,17α-pregnane-3,20-dione. J Chem Soc, Chem Commun (1985) 656-657
    • (1985) J Chem Soc, Chem Commun , pp. 656-657
    • Nagano, H.1    Iwadare, T.2    Shiota, M.3
  • 75
    • 34248509605 scopus 로고
    • Cyclization of 3,3:20,20-bis(ethylenedioxy)-C-nor-9,11-seco-5α-pregnane-9β,11-diol into 11-oxa-5α,17α-pregnane-3,20-dione
    • Nagano H., Iwadare T., and Shiota M. Cyclization of 3,3:20,20-bis(ethylenedioxy)-C-nor-9,11-seco-5α-pregnane-9β,11-diol into 11-oxa-5α,17α-pregnane-3,20-dione. J Chem Soc, Perkin Trans 1: Org Bio-Org Chem (1986) 2291-2293
    • (1986) J Chem Soc, Perkin Trans 1: Org Bio-Org Chem , pp. 2291-2293
    • Nagano, H.1    Iwadare, T.2    Shiota, M.3
  • 76
    • 0023213457 scopus 로고
    • Steroids and related products. The synthesis of 11-oxa steroids. The synthesis of 17-ethynyl-11-oxatestosterone
    • Engel C.R., Mukherjee D., Chowdhury M.N.R., and Salvi V.S. Steroids and related products. The synthesis of 11-oxa steroids. The synthesis of 17-ethynyl-11-oxatestosterone. Steroids 47 6 (1986) 381-399
    • (1986) Steroids , vol.47 , Issue.6 , pp. 381-399
    • Engel, C.R.1    Mukherjee, D.2    Chowdhury, M.N.R.3    Salvi, V.S.4
  • 77
    • 33947467691 scopus 로고
    • Sterols. Cortisone and analogs. 17α,21-Dihydroxy-4-pregnene-3,12,20-trione
    • Julian P.L., Cochrane C.C., Magnani A., and Karpel W.J. Sterols. Cortisone and analogs. 17α,21-Dihydroxy-4-pregnene-3,12,20-trione. J Am Chem Soc 78 (1956) 2153-2158
    • (1956) J Am Chem Soc , vol.78 , pp. 2153-2158
    • Julian, P.L.1    Cochrane, C.C.2    Magnani, A.3    Karpel, W.J.4
  • 78
    • 0000458625 scopus 로고
    • Steroids. Synthesis of 19-nor-17α-ethynyltestosterone and 19-nor-17α-methyltestosterone
    • Djerassi C., Miramontes L., Rosenkranz G., and Sondheimer F. Steroids. Synthesis of 19-nor-17α-ethynyltestosterone and 19-nor-17α-methyltestosterone. J Am Chem Soc 76 (1954) 4092-4094
    • (1954) J Am Chem Soc , vol.76 , pp. 4092-4094
    • Djerassi, C.1    Miramontes, L.2    Rosenkranz, G.3    Sondheimer, F.4
  • 79
    • 0023273601 scopus 로고
    • Steroids and related products. The synthesis of 11-oxa steroids. The synthesis of 11-oxatestosterone
    • Salvi V.S., Mukherjee D., and Engel C.R. Steroids and related products. The synthesis of 11-oxa steroids. The synthesis of 11-oxatestosterone. Steroids 48 (1986) 47-53
    • (1986) Steroids , vol.48 , pp. 47-53
    • Salvi, V.S.1    Mukherjee, D.2    Engel, C.R.3
  • 80
    • 0000180525 scopus 로고
    • Hydroformylation of the steroid nucleus: a novel method for the preparation of 6α methylsteroids
    • Nussbaum A.L., Popper T.L., Oliveto E.P., Friedman S., and Wender I. Hydroformylation of the steroid nucleus: a novel method for the preparation of 6α methylsteroids. J Am Chem Soc 81 (1959) 1228-1231
    • (1959) J Am Chem Soc , vol.81 , pp. 1228-1231
    • Nussbaum, A.L.1    Popper, T.L.2    Oliveto, E.P.3    Friedman, S.4    Wender, I.5
  • 81
    • 0039049382 scopus 로고
    • Photoinduced molecular transformations. Synthesis of heterosteroids. The first synthesis of 11-thiasteroids and a new synthesis of 11-oxasteroids
    • Suginome H., Wang J.B., and Yamada S. Photoinduced molecular transformations. Synthesis of heterosteroids. The first synthesis of 11-thiasteroids and a new synthesis of 11-oxasteroids. Chem Lett (1987) 783-786
    • (1987) Chem Lett , pp. 783-786
    • Suginome, H.1    Wang, J.B.2    Yamada, S.3
  • 82
    • 0025148906 scopus 로고
    • Photoinduced molecular transformations. A versatile substitution of a carbonyl group of steroidal ketones by a heteroatom. The synthesis of aza-, oxa-, thia-, selena-, and tellurasteroids
    • Suginome H., Yamada S., and Wang J.B. Photoinduced molecular transformations. A versatile substitution of a carbonyl group of steroidal ketones by a heteroatom. The synthesis of aza-, oxa-, thia-, selena-, and tellurasteroids. J Org Chem 55 7 (1990) 2170-2176
    • (1990) J Org Chem , vol.55 , Issue.7 , pp. 2170-2176
    • Suginome, H.1    Yamada, S.2    Wang, J.B.3
  • 83
    • 0000549969 scopus 로고
    • Intramolecular cycloadditions with isobenzofurans. Synthesis of precursors via an Oppe reaction
    • Hildebrandt K., and Friedrichsen W. Intramolecular cycloadditions with isobenzofurans. Synthesis of precursors via an Oppe reaction. Heterocycles 29 7 (1989) 1243-1246
    • (1989) Heterocycles , vol.29 , Issue.7 , pp. 1243-1246
    • Hildebrandt, K.1    Friedrichsen, W.2
  • 84
    • 0023922958 scopus 로고
    • Intramolecular cycloaddition with isobenzofuran. Synthesis of a 6-functionalized 11-oxasteroid
    • Hildebrandt K., Debaerdemaeker T., and Friedrichsen W. Intramolecular cycloaddition with isobenzofuran. Synthesis of a 6-functionalized 11-oxasteroid. Tetrahedron Lett 29 17 (1988) 2045-2046
    • (1988) Tetrahedron Lett , vol.29 , Issue.17 , pp. 2045-2046
    • Hildebrandt, K.1    Debaerdemaeker, T.2    Friedrichsen, W.3
  • 85
    • 0344054307 scopus 로고
    • A new synthesis of 3-oxo-3,4-dihydro-2H-1-benzopyrans, 3-oxo-3,4-dihydro-2H-naphtho[1,2-b]pyran, and 2-oxo-2,3-dihydro-1H-naphtho[2,1-b]pyran: the use of bis[hexafluoroacetoacetonato]copper(II) in the cyclization of 1-diazo-3-aryloxy-2-propanones
    • Saba A. A new synthesis of 3-oxo-3,4-dihydro-2H-1-benzopyrans, 3-oxo-3,4-dihydro-2H-naphtho[1,2-b]pyran, and 2-oxo-2,3-dihydro-1H-naphtho[2,1-b]pyran: the use of bis[hexafluoroacetoacetonato]copper(II) in the cyclization of 1-diazo-3-aryloxy-2-propanones. Synthesis (1984) 268-270
    • (1984) Synthesis , pp. 268-270
    • Saba, A.1
  • 86
    • 1542696263 scopus 로고
    • Intramolecular cycloadditions with isobenzofurans I
    • Friedrichsen W., Koenig B.M., and Hildebrandt K. Intramolecular cycloadditions with isobenzofurans I. Heterocycles 24 2 (1986) 297-302
    • (1986) Heterocycles , vol.24 , Issue.2 , pp. 297-302
    • Friedrichsen, W.1    Koenig, B.M.2    Hildebrandt, K.3
  • 87
    • 0006300496 scopus 로고
    • Steroids and related products. Synthesis of 11-oxasteroids. A novel pathway to 11-oxasteroids. Syntheses of 11-oxaestradiol and a new synthesis of 11-oxa-1-dehydro-11-deoxycortisol
    • Engel C.R., Ibrahim I.H., Mukherjee D., Szoghy R., and Salvi V.S. Steroids and related products. Synthesis of 11-oxasteroids. A novel pathway to 11-oxasteroids. Syntheses of 11-oxaestradiol and a new synthesis of 11-oxa-1-dehydro-11-deoxycortisol. Heterocycles 28 2 (1989) 905-922
    • (1989) Heterocycles , vol.28 , Issue.2 , pp. 905-922
    • Engel, C.R.1    Ibrahim, I.H.2    Mukherjee, D.3    Szoghy, R.4    Salvi, V.S.5
  • 88
    • 0016912196 scopus 로고
    • Heterocyclic steroids. Synthesis of (±)-8-hydroxy-3-methoxy-11-aza-18-norestra-1,3,5(10),9(11)-tetraen-17-one and related compounds
    • Nasipuri D., and Ghosh S.K. Heterocyclic steroids. Synthesis of (±)-8-hydroxy-3-methoxy-11-aza-18-norestra-1,3,5(10),9(11)-tetraen-17-one and related compounds. J Chem Soc, Perkin Trans 1: Org Bio-Org Chem (1976) 1889-1893
    • (1976) J Chem Soc, Perkin Trans 1: Org Bio-Org Chem , pp. 1889-1893
    • Nasipuri, D.1    Ghosh, S.K.2
  • 89
    • 0020403320 scopus 로고
    • Chlorodecarboxylation of 17β-acetoxy-3-methoxy-9-oxo-9,11-secoestra-1,3,5(10)-trien-11-oic acid with lead tetraacetate and trityl chloride
    • Lal K., and Ray S. Chlorodecarboxylation of 17β-acetoxy-3-methoxy-9-oxo-9,11-secoestra-1,3,5(10)-trien-11-oic acid with lead tetraacetate and trityl chloride. Steroids 39 5 (1982) 537-545
    • (1982) Steroids , vol.39 , Issue.5 , pp. 537-545
    • Lal, K.1    Ray, S.2
  • 90
    • 37049047093 scopus 로고
    • Photochemical transformations. Improved methods for the decarboxylation of acids
    • Barton D.H.R., Faro H.P., Serebryakov E.P., and Woolsey N.F. Photochemical transformations. Improved methods for the decarboxylation of acids. J Chem Soc (1965) 2438-2444
    • (1965) J Chem Soc , pp. 2438-2444
    • Barton, D.H.R.1    Faro, H.P.2    Serebryakov, E.P.3    Woolsey, N.F.4
  • 91
    • 0028915466 scopus 로고
    • Heterocyclic steroids. Synthesis and estrogen receptor binding affinities of 8-aza-11-oxasteroids and 8-aza-11-oxa-D-homosteroids
    • Campagna F., Carotti A., Casini G., and Otto A.M. Heterocyclic steroids. Synthesis and estrogen receptor binding affinities of 8-aza-11-oxasteroids and 8-aza-11-oxa-D-homosteroids. Farmaco 50 2 (1995) 137-141
    • (1995) Farmaco , vol.50 , Issue.2 , pp. 137-141
    • Campagna, F.1    Carotti, A.2    Casini, G.3    Otto, A.M.4
  • 92
    • 0022871173 scopus 로고
    • Synthesis of 12-mono- and disubstituted 8-aza-11-oxasteroids
    • Campagna F., Altomare C., Carotti A., Casini G., and Ferappi M. Synthesis of 12-mono- and disubstituted 8-aza-11-oxasteroids. Steroids 47 4/5 (1986) 307-320
    • (1986) Steroids , vol.47 , Issue.4-5 , pp. 307-320
    • Campagna, F.1    Altomare, C.2    Carotti, A.3    Casini, G.4    Ferappi, M.5
  • 93
    • 0001150847 scopus 로고
    • An efficient synthesis of substituted isoquinolines
    • Hendrickson J.B., and Rodriguez C. An efficient synthesis of substituted isoquinolines. J Org Chem 48 19 (1983) 3344-3346
    • (1983) J Org Chem , vol.48 , Issue.19 , pp. 3344-3346
    • Hendrickson, J.B.1    Rodriguez, C.2
  • 94
    • 0033592617 scopus 로고    scopus 로고
    • Unprecedented and novel hetero [6+3] cycloadditions of fulvene: a facile synthesis of the 11-oxasteroid framework
    • Hong B.C., Sun H.I., and Chen Z.Y. Unprecedented and novel hetero [6+3] cycloadditions of fulvene: a facile synthesis of the 11-oxasteroid framework. Chem Commun (1999) 2125-2126
    • (1999) Chem Commun , pp. 2125-2126
    • Hong, B.C.1    Sun, H.I.2    Chen, Z.Y.3
  • 95
  • 96
    • 0001179810 scopus 로고
    • Intramolecular cycloadditions of o-quinodimethanes
    • Oppolzer W. Intramolecular cycloadditions of o-quinodimethanes. J Am Chem Soc 93 15 (1971) 3833-3834
    • (1971) J Am Chem Soc , vol.93 , Issue.15 , pp. 3833-3834
    • Oppolzer, W.1
  • 97
    • 0001080486 scopus 로고
    • Thermal rearrangement of N-(1-benzocyclobutenyl)vinylacetamide. Kinetics and mechanism
    • Oppolzer W. Thermal rearrangement of N-(1-benzocyclobutenyl)vinylacetamide. Kinetics and mechanism. J Am Chem Soc 93 15 (1971) 3834-3835
    • (1971) J Am Chem Soc , vol.93 , Issue.15 , pp. 3834-3835
    • Oppolzer, W.1
  • 98
    • 0017098147 scopus 로고
    • A formal regio- and stereoselective total synthesis of estrone. A convenient synthesis of D-homoestrone
    • Kametani T., Nemoto H., Ishikawa H., Shiroyama K., and Fukumoto K. A formal regio- and stereoselective total synthesis of estrone. A convenient synthesis of D-homoestrone. J Am Chem Soc 98 11 (1976) 3378-3379
    • (1976) J Am Chem Soc , vol.98 , Issue.11 , pp. 3378-3379
    • Kametani, T.1    Nemoto, H.2    Ishikawa, H.3    Shiroyama, K.4    Fukumoto, K.5
  • 99
    • 0017772407 scopus 로고
    • A stereoselective total synthesis of estrone by an intramolecular cycloaddition reaction of olefinic o-quinodimethane
    • Kametani T., Nemoto H., Ishikawa H., Shiroyama K., Matsumoto H., and Fukumoto K. A stereoselective total synthesis of estrone by an intramolecular cycloaddition reaction of olefinic o-quinodimethane. J Am Chem Soc 99 10 (1977) 3461-3466
    • (1977) J Am Chem Soc , vol.99 , Issue.10 , pp. 3461-3466
    • Kametani, T.1    Nemoto, H.2    Ishikawa, H.3    Shiroyama, K.4    Matsumoto, H.5    Fukumoto, K.6
  • 100
    • 0002375921 scopus 로고
    • New synthetic methods. Intramolecular [4+2]- and [3+2]-cycloadditions in organic synthesis
    • Oppolzer W. New synthetic methods. Intramolecular [4+2]- and [3+2]-cycloadditions in organic synthesis. Angew Chem 89 1 (1977) 10-24
    • (1977) Angew Chem , vol.89 , Issue.1 , pp. 10-24
    • Oppolzer, W.1
  • 101
    • 85065852858 scopus 로고
    • Intramolecular cycloaddition reactions of o-quinodimethans in organic synthesis
    • Oppolzer W. Intramolecular cycloaddition reactions of o-quinodimethans in organic synthesis. Synthesis (1978) 793-802
    • (1978) Synthesis , pp. 793-802
    • Oppolzer, W.1
  • 102
    • 0019432563 scopus 로고
    • Recent advances in the total synthesis of steroids via intramolecular cycloaddition reactions
    • Kametani T., and Nemoto H. Recent advances in the total synthesis of steroids via intramolecular cycloaddition reactions. Tetrahedron 37 1 (1981) 3-16
    • (1981) Tetrahedron , vol.37 , Issue.1 , pp. 3-16
    • Kametani, T.1    Nemoto, H.2
  • 103
    • 0032554910 scopus 로고    scopus 로고
    • Second generation of steroid synthesis via o-quinodimethane
    • Nemoto H., and Fukumoto K. Second generation of steroid synthesis via o-quinodimethane. Tetrahedron 54 21 (1998) 5425-5464
    • (1998) Tetrahedron , vol.54 , Issue.21 , pp. 5425-5464
    • Nemoto, H.1    Fukumoto, K.2
  • 104
    • 0037068141 scopus 로고    scopus 로고
    • First [2+2]-cycloaddition of a 3,4-didehydropyridine and a ketene dialkyl acetal
    • Mariet N., Ibrahim-Ouali M., and Santelli M. First [2+2]-cycloaddition of a 3,4-didehydropyridine and a ketene dialkyl acetal. Tetrahedron Lett 43 33 (2002) 5789-5791
    • (2002) Tetrahedron Lett , vol.43 , Issue.33 , pp. 5789-5791
    • Mariet, N.1    Ibrahim-Ouali, M.2    Santelli, M.3
  • 105
    • 33747844631 scopus 로고    scopus 로고
    • First total synthesis of 3-aza-11-oxa-1,3,5(10)-trieno steroids
    • Oumzil K., Ibrahim-Ouali M., and Santelli M. First total synthesis of 3-aza-11-oxa-1,3,5(10)-trieno steroids. Steroids 71 10 (2006) 886-894
    • (2006) Steroids , vol.71 , Issue.10 , pp. 886-894
    • Oumzil, K.1    Ibrahim-Ouali, M.2    Santelli, M.3
  • 106
    • 0006387595 scopus 로고
    • Stereochemical studies. Saturated heterocycles. A simple stereospecific synthesis of oxazasteroids
    • Bernath G., Fueloep F., Argay G., Kalman A., and Sohar P. Stereochemical studies. Saturated heterocycles. A simple stereospecific synthesis of oxazasteroids. Tetrahedron Lett 22 38 (1981) 3797-3800
    • (1981) Tetrahedron Lett , vol.22 , Issue.38 , pp. 3797-3800
    • Bernath, G.1    Fueloep, F.2    Argay, G.3    Kalman, A.4    Sohar, P.5
  • 109
    • 34248516175 scopus 로고
    • Attempts to induce the pimarane-cassane ring system transformation
    • Ceccherelli P., Curini M., Tingoli M., and Pellicciari R. Attempts to induce the pimarane-cassane ring system transformation. Gazz Chim Ital 108 (1978) 129-130
    • (1978) Gazz Chim Ital , vol.108 , pp. 129-130
    • Ceccherelli, P.1    Curini, M.2    Tingoli, M.3    Pellicciari, R.4
  • 110
    • 0026317255 scopus 로고
    • An approach to oxasteroids
    • King J.D., and Quayle P. An approach to oxasteroids. Tetrahedron Lett 32 52 (1991) 7759-7762
    • (1991) Tetrahedron Lett , vol.32 , Issue.52 , pp. 7759-7762
    • King, J.D.1    Quayle, P.2
  • 111
    • 33646791205 scopus 로고
    • Influence of the degree of substitution of the ethylenic double bond on the stereochemistry of 1,4-hydrocyanation of conjugated ketones
    • Agami C., Fadlallah M., Levisalles J., and Stereochemistry. Influence of the degree of substitution of the ethylenic double bond on the stereochemistry of 1,4-hydrocyanation of conjugated ketones. Tetrahedron 37 5 (1981) 909-914
    • (1981) Tetrahedron , vol.37 , Issue.5 , pp. 909-914
    • Agami, C.1    Fadlallah, M.2    Levisalles, J.3    Stereochemistry4
  • 112
    • 34248548187 scopus 로고
    • Totally synthetic steroid heterocycles. Facile approach to 16-oxa-D-homoestrogens
    • Terasawa T., and Okada T. Totally synthetic steroid heterocycles. Facile approach to 16-oxa-D-homoestrogens. J Heterocycl Chem 6 4 (1979) 37-40
    • (1979) J Heterocycl Chem , vol.6 , Issue.4 , pp. 37-40
    • Terasawa, T.1    Okada, T.2
  • 113
    • 33644509048 scopus 로고
    • Totally synthetic steroid heterocycles. Synthesis of intermediate precursors of 16-oxa- and 16-thia-D-homoestrogens
    • Terasawa T., and Okada T. Totally synthetic steroid heterocycles. Synthesis of intermediate precursors of 16-oxa- and 16-thia-D-homoestrogens. J Chem Soc, Perkin Trans 1: Org Bio-Org Chem (1978) 576-584
    • (1978) J Chem Soc, Perkin Trans 1: Org Bio-Org Chem , pp. 576-584
    • Terasawa, T.1    Okada, T.2
  • 114
    • 34248556810 scopus 로고
    • Heterocyclic analogs of steroids. Synthesis and some properties of 8-aza-16-oxagonane-12,17-dione derivatives
    • Akhrem A.A., Lakhvich F.A., Lis L.G., and Pshenichnyi V.N. Heterocyclic analogs of steroids. Synthesis and some properties of 8-aza-16-oxagonane-12,17-dione derivatives. Zhurnal Organicheskoi Khimii 5 7 (1979) 396-402
    • (1979) Zhurnal Organicheskoi Khimii , vol.5 , Issue.7 , pp. 396-402
    • Akhrem, A.A.1    Lakhvich, F.A.2    Lis, L.G.3    Pshenichnyi, V.N.4
  • 115
    • 37049088107 scopus 로고
    • New short step synthesis of A,B-aromatic oxasteroids by intra- and intermolecular Diels-Alder reactions of 1,2-naphthoquinone dimethides generated from substituted 1,2-cyclobutanaphthalenes
    • Kobayashi K., Itoh M., and Suginome H. New short step synthesis of A,B-aromatic oxasteroids by intra- and intermolecular Diels-Alder reactions of 1,2-naphthoquinone dimethides generated from substituted 1,2-cyclobutanaphthalenes. J Chem Soc, Perkin Trans 1: Org Bio-Org Chem (1991) 135-138
    • (1991) J Chem Soc, Perkin Trans 1: Org Bio-Org Chem , pp. 135-138
    • Kobayashi, K.1    Itoh, M.2    Suginome, H.3
  • 116
    • 34248560388 scopus 로고
    • Photoinduced molecular transformations. Ring expansion through [2+2] photocycloaddition-β-scission sequences; synthesis of benzohomotropones from 1- and 2-naphthols and methyl acrylate
    • Suginome H., Itoh M., and Kobayashi K. Photoinduced molecular transformations. Ring expansion through [2+2] photocycloaddition-β-scission sequences; synthesis of benzohomotropones from 1- and 2-naphthols and methyl acrylate. J Chem Soc, Perkin Trans 1: Org Bio-Org Chem (1988) 491-496
    • (1988) J Chem Soc, Perkin Trans 1: Org Bio-Org Chem , pp. 491-496
    • Suginome, H.1    Itoh, M.2    Kobayashi, K.3
  • 117
    • 34248518009 scopus 로고    scopus 로고
    • Total synthesis of d,l-isospongiadiol: an intramolecular radical cascade approach to furanoditerpenes
    • Zoretic P.A., Wang M., Zhang Y., Shen Z., and Ribeiro A.A. Total synthesis of d,l-isospongiadiol: an intramolecular radical cascade approach to furanoditerpenes. J Org Chem 1 5 (1996) 806-813
    • (1996) J Org Chem , vol.1 , Issue.5 , pp. 806-813
    • Zoretic, P.A.1    Wang, M.2    Zhang, Y.3    Shen, Z.4    Ribeiro, A.A.5
  • 118
    • 0002519096 scopus 로고
    • Cross Sue. Isospongiadiol, a cytotoxic and antiviral diterpene from a Caribbean deep water marine sponge, Spongia sp
    • Kohmoto S., McConnell O.J., and Wright A. Cross Sue. Isospongiadiol, a cytotoxic and antiviral diterpene from a Caribbean deep water marine sponge, Spongia sp. Chem Lett (1987) 1687-1690
    • (1987) Chem Lett , pp. 1687-1690
    • Kohmoto, S.1    McConnell, O.J.2    Wright, A.3
  • 119
    • 34248505370 scopus 로고
    • Synthesis of cembrane natural products via [2,3] Wittig ring contraction of propargylic ethers
    • Marshall J.A., Jenson T.M., and DeHoff B.S. Synthesis of cembrane natural products via [2,3] Wittig ring contraction of propargylic ethers. J Org Chem 2 17 (1987) 860-866
    • (1987) J Org Chem , vol.2 , Issue.17 , pp. 860-866
    • Marshall, J.A.1    Jenson, T.M.2    DeHoff, B.S.3
  • 120
    • 0038818553 scopus 로고    scopus 로고
    • The domino intramolecular Diels-Alder approach to 16-oxasteroids
    • Turner C.I., Williamson R.M., Turner P., and Sherburn M.S. The domino intramolecular Diels-Alder approach to 16-oxasteroids. Chem Commun (2003) 1610-1611
    • (2003) Chem Commun , pp. 1610-1611
    • Turner, C.I.1    Williamson, R.M.2    Turner, P.3    Sherburn, M.S.4
  • 121
    • 0001231218 scopus 로고
    • Catalysis by mercuric ion of reactions of glycals with water
    • Gonzalez F., Lesage S., and Perlin A.S. Catalysis by mercuric ion of reactions of glycals with water. Carbohydr Res 42 (1975) 267-274
    • (1975) Carbohydr Res , vol.42 , pp. 267-274
    • Gonzalez, F.1    Lesage, S.2    Perlin, A.S.3
  • 122
    • 84961489382 scopus 로고
    • Four isomeric 1,3,5-undecatrienes. Synthesis and configurational assignment
    • Naef F., Decorzant R., Thommen W., Willhalm B., and Ohloff G. Four isomeric 1,3,5-undecatrienes. Synthesis and configurational assignment. Helvetica Chim Acta 58 4 (1975) 1016-1037
    • (1975) Helvetica Chim Acta , vol.58 , Issue.4 , pp. 1016-1037
    • Naef, F.1    Decorzant, R.2    Thommen, W.3    Willhalm, B.4    Ohloff, G.5
  • 123
    • 0006697228 scopus 로고
    • A new methodology to key intermediates for synthesizing polyene compounds
    • Ma D., and Lu X. A new methodology to key intermediates for synthesizing polyene compounds. Tetrahedron 46 18 (1990) 6319-6330
    • (1990) Tetrahedron , vol.46 , Issue.18 , pp. 6319-6330
    • Ma, D.1    Lu, X.2
  • 124
    • 37049076286 scopus 로고
    • Stereochemical aspects of the intramolecular Diels-Alder reaction
    • Craig D. Stereochemical aspects of the intramolecular Diels-Alder reaction. Chem Soc Rev 16 2 (1987) 187-238
    • (1987) Chem Soc Rev , vol.16 , Issue.2 , pp. 187-238
    • Craig, D.1
  • 125
    • 0032838140 scopus 로고    scopus 로고
    • Harvesting Diels and Alder's Garden: synthetic investigations of intramolecular [4+2] cycloadditions
    • Fallis A.G. Harvesting Diels and Alder's Garden: synthetic investigations of intramolecular [4+2] cycloadditions. Acc Chem Res 32 6 (1999) 464-474
    • (1999) Acc Chem Res , vol.32 , Issue.6 , pp. 464-474
    • Fallis, A.G.1
  • 126
    • 0035793788 scopus 로고    scopus 로고
    • The type 2 intramolecular Diels-Alder reaction: synthesis and chemistry of bridgehead alkenes
    • Bear B.R., Sparks S.M., and Shea K.J. The type 2 intramolecular Diels-Alder reaction: synthesis and chemistry of bridgehead alkenes. Angew Chem Int Ed 40 5 (2001) 820-849
    • (2001) Angew Chem Int Ed , vol.40 , Issue.5 , pp. 820-849
    • Bear, B.R.1    Sparks, S.M.2    Shea, K.J.3
  • 127
    • 0039435260 scopus 로고
    • Novel conversion of 17-oxo steroids into the corresponding α,β-unsaturated D-homo-lactone by selenylation-dehydro-selenylation
    • Williams J.R., and Leber J.D. Novel conversion of 17-oxo steroids into the corresponding α,β-unsaturated D-homo-lactone by selenylation-dehydro-selenylation. Synthesis (1977) 427-428
    • (1977) Synthesis , pp. 427-428
    • Williams, J.R.1    Leber, J.D.2
  • 128
    • 33847802966 scopus 로고
    • Organoselenium chemistry. Conversion of ketones to enones by selenoxide syn elimination
    • Reich H.J., Renga J.M., and Reich I.L. Organoselenium chemistry. Conversion of ketones to enones by selenoxide syn elimination. J Am Chem Soc 97 19 (1975) 5434-5447
    • (1975) J Am Chem Soc , vol.97 , Issue.19 , pp. 5434-5447
    • Reich, H.J.1    Renga, J.M.2    Reich, I.L.3
  • 129
    • 33947085849 scopus 로고
    • Electrophilic and nucleophilic organoselenium reagents. New routes to α,β-unsaturated carbonyl compounds
    • Sharpless K.B., Lauer R.F., and Teranishi A.Y. Electrophilic and nucleophilic organoselenium reagents. New routes to α,β-unsaturated carbonyl compounds. J Am Chem Soc 95 18 (1973) 6137-6139
    • (1973) J Am Chem Soc , vol.95 , Issue.18 , pp. 6137-6139
    • Sharpless, K.B.1    Lauer, R.F.2    Teranishi, A.Y.3
  • 130
    • 27844535784 scopus 로고    scopus 로고
    • ynthesis of some novel D-dihomo-aza- and D-dihomo-oxa-steroid derivatives in the estrone series
    • Frank E., Schneider G., Messinger J., Thole H., and Wolfling J. ynthesis of some novel D-dihomo-aza- and D-dihomo-oxa-steroid derivatives in the estrone series. Synlett (2005) 2814-2816
    • (2005) Synlett , pp. 2814-2816
    • Frank, E.1    Schneider, G.2    Messinger, J.3    Thole, H.4    Wolfling, J.5
  • 131
    • 4644250439 scopus 로고
    • Cleavage of the D ring in 16-substituted steroids
    • Guzzi U., and Marnini G. Cleavage of the D ring in 16-substituted steroids. Gazz Chim Ital 107 1/2 (1977) 75-81
    • (1977) Gazz Chim Ital , vol.107 , Issue.1-2 , pp. 75-81
    • Guzzi, U.1    Marnini, G.2
  • 132
    • 84987279773 scopus 로고
    • A convenient method for the formation of 16-methylene-17-keto steroids
    • Schneider G., Vincze I., Hackler L., and Dombi G. A convenient method for the formation of 16-methylene-17-keto steroids. Synthesis (1983) 665-669
    • (1983) Synthesis , pp. 665-669
    • Schneider, G.1    Vincze, I.2    Hackler, L.3    Dombi, G.4
  • 133
    • 0342579710 scopus 로고
    • Novel chemistry and new biological activities of some 2-oxasteroids
    • Pappo R. Novel chemistry and new biological activities of some 2-oxasteroids. Intra-Sci Chem Rep 3 1/2 (1969) 105-122
    • (1969) Intra-Sci Chem Rep , vol.3 , Issue.1-2 , pp. 105-122
    • Pappo, R.1
  • 134
    • 0018659774 scopus 로고
    • Heterosteroids and drug research
    • Singh H., Kapoor V.K., and Paul D. Heterosteroids and drug research. Prog Med Chem 16 (1979) 35-149
    • (1979) Prog Med Chem , vol.16 , pp. 35-149
    • Singh, H.1    Kapoor, V.K.2    Paul, D.3
  • 138
    • 0030938127 scopus 로고    scopus 로고
    • A new synthetic steroid, osaterone acetate (TZP-4238), increases cortical bone mass and strength by enhancing bone formation in ovariectomized rats
    • Fuse H., Fukumoto S., Sone H., Miyata Y., Saito T., Nakayama K., et al. A new synthetic steroid, osaterone acetate (TZP-4238), increases cortical bone mass and strength by enhancing bone formation in ovariectomized rats. J Bone Miner Res 12 4 (1997) 590-597
    • (1997) J Bone Miner Res , vol.12 , Issue.4 , pp. 590-597
    • Fuse, H.1    Fukumoto, S.2    Sone, H.3    Miyata, Y.4    Saito, T.5    Nakayama, K.6
  • 139
    • 0028167482 scopus 로고
    • Raloxifene (LY139481 HCl) prevents bone loss and reduces serum cholesterol without causing uterine hypertrophy in ovariectomized rats
    • Black L.J., Sato M., Rowley E.R., Magee D.E., Bekele A., Williams D.C., et al. Raloxifene (LY139481 HCl) prevents bone loss and reduces serum cholesterol without causing uterine hypertrophy in ovariectomized rats. J Clin Invest 93 1 (1994) 63-69
    • (1994) J Clin Invest , vol.93 , Issue.1 , pp. 63-69
    • Black, L.J.1    Sato, M.2    Rowley, E.R.3    Magee, D.E.4    Bekele, A.5    Williams, D.C.6
  • 140
    • 0028237839 scopus 로고
    • Ipriflavone prevents the bone mass reduction in premenopausal women treated with gonadotropin hormone-releasing hormone agonists
    • Gambacciani M., Spinetti A., Piaggesi L., Cappagli B., Taponeco, Manetti P., et al. Ipriflavone prevents the bone mass reduction in premenopausal women treated with gonadotropin hormone-releasing hormone agonists. Bone Miner 26 1 (1994) 19-26
    • (1994) Bone Miner , vol.26 , Issue.1 , pp. 19-26
    • Gambacciani, M.1    Spinetti, A.2    Piaggesi, L.3    Cappagli, B.4    Taponeco5    Manetti, P.6
  • 141
    • 0024454114 scopus 로고
    • Chemical model systems for drug-metabolizing cytochrome-P-450-dependent monooxygenases
    • Mansuy D., Battioni P., and Battioni J.P. Chemical model systems for drug-metabolizing cytochrome-P-450-dependent monooxygenases. Eur J Biochem 184 2 (1989) 267-285
    • (1989) Eur J Biochem , vol.184 , Issue.2 , pp. 267-285
    • Mansuy, D.1    Battioni, P.2    Battioni, J.P.3
  • 142
    • 0028286267 scopus 로고
    • 6-Alkyl- and 6-arylandrost-4-ene-3,17-diones as aromatase inhibitors. Synthesis and structure-activity relationships
    • Numazawa M., and Oshibe M. 6-Alkyl- and 6-arylandrost-4-ene-3,17-diones as aromatase inhibitors. Synthesis and structure-activity relationships. J Med Chem 37 9 (1994) 1312-1319
    • (1994) J Med Chem , vol.37 , Issue.9 , pp. 1312-1319
    • Numazawa, M.1    Oshibe, M.2
  • 143
    • 0028029903 scopus 로고
    • A- or B-ring-substituted derivatives of androst-4-ene-3,6,17-trione as aromatase inhibitors. Structure-activity relationships
    • Numazawa M., and Tachibana M. A- or B-ring-substituted derivatives of androst-4-ene-3,6,17-trione as aromatase inhibitors. Structure-activity relationships. Steroids 59 10 (1994) 579-585
    • (1994) Steroids , vol.59 , Issue.10 , pp. 579-585
    • Numazawa, M.1    Tachibana, M.2
  • 144
    • 0007495713 scopus 로고
    • Biological effects of racemic and resolved 13β-ethyl-4-gonen-3-ones
    • Edgren R.A., Smith H., Hughes G.A., Smith L.L., and Greenspan G. Biological effects of racemic and resolved 13β-ethyl-4-gonen-3-ones. Steroids 2 6 (1963) 731-737
    • (1963) Steroids , vol.2 , Issue.6 , pp. 731-737
    • Edgren, R.A.1    Smith, H.2    Hughes, G.A.3    Smith, L.L.4    Greenspan, G.5
  • 145
    • 0018697620 scopus 로고
    • Brassinolide, a plant growth-promoting steroid isolated from Brassica napus pollen
    • Grove M.D., Spencer G.F., Rohwedder W.K., Mandava N., Worley J.F., Warthen J.D., et al. Brassinolide, a plant growth-promoting steroid isolated from Brassica napus pollen. Nature 281 5728 (1979) 216-217
    • (1979) Nature , vol.281 , Issue.5728 , pp. 216-217
    • Grove, M.D.1    Spencer, G.F.2    Rohwedder, W.K.3    Mandava, N.4    Worley, J.F.5    Warthen, J.D.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.