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ORBITS OF THREE SOUTHERN VISUAL BINARIESWORLEY CE.1982; PUBL. ASTRON. SOC. PAC.; ISSN 0004-6280; USA; DA. 1982; VOL. 93; NO 556; PP. 772-773; BIBL. 3 REF.Article

USE OF N-LITHIOETHYLENEDIAMINE IN THE DOUBLE BOND ISOMERIZATION AND DEGRADATION OF STEROL SIDE CHAINSAYANOGLU E; CHAN A; DJERASSI C et al.1979; TETRAHEDRON; GBR; DA. 1979; VOL. 35; NO 13; PP. 1591-1594; BIBL. 17 REF.Article

STEREOSPECIFIC SYNTHESIS OF (Z)-20(22)-DIDEHYDROCHOLESTEROL.KOREEDA M; KOIZUMI N; TEICHER B et al.1976; J. CHEM. COMMUNIC.; G.B.; DA. 1976; NO 24; PP. 1035-1036; BIBL. 7 REF.Article

ACID CATALYSED ISOMERISATION OF 3-EPI-MORETENYL ACETATE.KHASTGIR HN; PRADHAN BP.1977; J. INDIAN CHEM. SOC.; INDIA; DA. 1977; VOL. 54; NO 9; PP. 922; BIBL. 5 REF.Article

INFLUENCE DE L'INSATURATION DELTA 20 (22) SUR LA FRAGMENTATION DU CYCLE D DES STEROIDES.SCHMIT JP; CHARETTE JJ.1977; ORG. MASS SPECTROM.; G.B.; DA. 1977; VOL. 12; NO 8; PP. 488-492; ABS. ANGL.; BIBL. 5 REF.Article

STEREOSPECIFIC SYNTHESIS OF THE FOUR 20,22-EPOXYCHOLESTEROLS AND OF (Z)-20(22)-DEHYDROCHOLESTEROL.CHANG YON BYON; GUT M.1976; J. ORG. CHEM.; U.S.A.; DA. 1976; VOL. 41; NO 23; PP. 3716-3722; BIBL. 27 REF.Article

CONFORMATIONAL EQUILIBRIUM OF THE 17(20) ROTAMERS OF (E)-20(22)-DEHYDROCHOLESTEROL.NES WR.1978; J. AMER. CHEM. SOC.; U.S.A.; DA. 1978; VOL. 100; NO 3; PP. 999-1000; BIBL. 11 REF.Article

Cleavage reaction of 5β,6β steroidal epoxides carrying different groups at C-3TEME CENTURION, O. M; GALAGOVSKY, L. R; GROS, E. G et al.Steroids. 1995, Vol 60, Num 7, pp 434-438, issn 0039-128XArticle

SYNTHESES DE TRITERPENES POTENTIELLEMENT ANTI-CANCEREUXDE REINACH HIRTZBACH F.1973; AO-CNRS-10528; FR.; DA. 1973; PP. 1-132; BIBL. 6 P. 1/2; (THESE DOCT. SCI. PHYS.; LOUIS PASTEUR STRASBOURG)Thesis

Acetylenic cholesteryl derivatives as irreversible inhibitors of ecdysone biosynthesisBURGER, A; COLOBERT, F; HETRU, C et al.Tetrahedron (Oxford. Print). 1988, Vol 44, Num 4, pp 1141-1152, issn 0040-4020Article

THE STEREOCHEMISTRY OF STEROLS AT C-20 AND ITS BIOSYNTHETIC IMPLICATION.NES WR; VARKEY TE; KREVITZ K et al.1977; J. AMER. CHEM. SOC.; U.S.A.; DA. 1977; VOL. 99; NO 1; PP. 260-262; BIBL. 18 REF.Article

APPLICATION OF THE WITTIG REACTION TO THE SYNTHESIS OF STEROIDAL SIDE CHAINS. POSSIBILITY OF 3BETA -PHENOXY FORMATION AS A SECONDARY REACTIONSCHMIT JP; PIRAUX M; PILETTE JF et al.1975; J. ORG. CHEM.; U.S.A.; DA. 1975; VOL. 40; NO 11; PP. 1586-1588; BIBL. 11 REF.Article

Synthesis from pregnenolone of fluorescent cholesterol analogue probes with conjugated unsaturation in the side chainDREW, J; LETELLIER, M; MORAND, P et al.Journal of organic chemistry. 1987, Vol 52, Num 18, pp 4047-4052, issn 0022-3263Article

Regiocontrolled synthesis of the ergosterol B-isomersDOLLE, R. E; SCHMIDT, S. J; KRUSE, L. I et al.Tetrahedron letters. 1988, Vol 29, Num 13, pp 1581-1582, issn 0040-4039Article

ERGOSTA-5,7,9(11),22-TETRAEN-3BETA -OL AND ITS 24XI -ETHYL HOMOLOG, TWO NEW MARINE STEROLS FROM THE RED SEA SPONGE BIEMNA FORTISDELSETH C; KASHMAN Y; DJERASSSI C et al.1979; HELV. CHIM. ACTA; CHE; DA. 1979; VOL. 62; NO 6; PP. 2037-2045; BIBL. 34 REF.Article

SELECTIVITY IN THE HYDROGENATION OF 20(22)-DEHYDROSTEROIDSDUBOIS GE.1982; J. ORG. CHEM.; ISSN 0022-3263; USA; DA. 1982; VOL. 47; NO 25; PP. 5035-5037; BIBL. 21 REF.Article

Fern constituents: Triterpenoids isolated from rhizomes of Pyrrosia lingua. IMASUDA, K; YAMASHITA, H; SHIOJIMA, K et al.Chemical and pharmaceutical bulletin. 1997, Vol 45, Num 4, pp 590-594, issn 0009-2363Article

Fern constituents : triterpenoids isolated from Polypodium vulgare, P. fauriei and P. virginianumARAI, Y; YAMAIDE, M; YAMAZAKI, S et al.Phytochemistry. 1991, Vol 30, Num 10, pp 3369-3377, issn 0031-9422Article

EMPIRICAL QUANTUM CHEMICAL APPROACH TO STRUCTURE-GAS CHROMATOGRAPHIC RETENTION INDEX RELATIONSHIPSGASSIOT M; FERNANDEZ E; FIRPO G et al.1975; J. CHROMATOGR.; NETHERL.; DA. 1975; VOL. 108; NO 2; PP. 337-344; BIBL. 26 REF.Article

Double bond migration on the 22(17→28) abeo-lupane skeletonFUCHINO, H; NOZAWA, O; TANAKA, N et al.Chemical and pharmaceutical bulletin. 1994, Vol 42, Num 9, pp 1745-1749, issn 0009-2363Article

Ene approach for concurrent control over the chiral centres at C-20 and C-22 of steroid side chains: a highly stereocontrolled synthesis of (20S,22R)-(erythro-)22-hydroxy-23,24-acetylenic steroid side chainsMIKAMI, K; LOH, T.-P; NAKAI, T et al.Journal of the Chemical Society. Chemical communications. 1988, Num 21, pp 1430-1431, issn 0022-4936Article

STEREOCHEMISTRY OF 14,22-ETHERS FORMED BY CYCLIZATION OF DELTA 7-22-HYDROXY STEROIDSABERHART DJ; CASPI E; WEEKS CM et al.1979; J. ORG. CHEM.; USA; DA. 1979; VOL. 44; NO 1; PP. 75-77; BIBL. 6 REF.Article

CORRELATIONS BETWEEN CHEMICAL STRUCTURE AND K-VALUE IN THE TLC OF EPIMERIC 3-ETHINYL-3-CHOLESTANOLSBERBALIK H; EICHINGER K; SCHUSTER R et al.1979; H.R.C. AND C.C.; DEU; DA. 1979; VOL. 2; NO 8; PP. 535-536; BIBL. 8 REF.Article

REACTION OF CHOLESTEROL WITH SODIUM ETHOXIDE: THE GUERBET-MARKOVNIKOV REACTION IN STEROIDSWICHA J; PIEKUT S.1976; ROCZ. CHEM.; POLSKA; DA. 1976; VOL. 50; NO 2; PP. 221-233; ABS. POL. RUSSE; BIBL. 24 REF.Article

Oygenated sterols as inhibitors of enzymatic conversion of dihydrolanosterol into cholesterolSATO, Y; SONODA, Y; MORISAKI, M et al.Chemical and pharmaceutical bulletin. 1984, Vol 32, Num 8, pp 3305-3308, issn 0009-2363Article

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