메뉴 건너뛰기




Volumn 70, Issue 2, 2005, Pages 111-116

Some unreported by-products from the reaction of 1,4-dien-3-one steroids with 2-(methylammo)benzethiol/BF3

Author keywords

1,4 Dien 3 one steroids; 2 (Methylamino)benzethiol; Benzathiazol fused steroids; Carbonyl protection; Steroids

Indexed keywords

3' METHYLBENZATHIAZOL[4,3 B]ANDROSTA 3,5 DIEN 1 [2 (METHYLAMINO)BENZETHIOL] 17 ONE; 3' METHYLBENZATHIAZOL[4,3 B]ESTRA 1 METHYL 9(11) EN 17ALPHA ACETOXY 17BETA NITRIL; 3' METHYLBENZATHIAZOL[4,3 B]ESTRA 1 METHYL 9(11) EN 17ALPHA OL 17BETA NITRIL; 3' METHYLSPIRO[ANDROSTA 1,4 DIEN 3,2'(3'H)BENZOTHIAZOL] 9(11) EN 17 ONE; 3' METHYLSPIRO[ANDROSTA 1,4 DIEN 3,2'(3'H)BENZOTHIAZOL] 9(11) EN 17ALPHA ACETOXY 17BETA NITRIL; 3' METHYLSPIRO[ANDROSTA 1,4 DIEN 3,2'(3'H)BENZOTHIAZOL] 9(11) EN 17ALPHA OL 17BETA NITRIL; ANDROSTA 1,4,9(11) TRIEN 3 ON 17ALPHA ACETOXY 17BETA NITRIL; ANDROSTA 1,4,9(11) TRIEN 3 ON 17ALPHA OL 17BETA NITRIL; ANDROSTA 3,5 DIEN 1,3 DI[2 (METHYLAMINO)BENZETHIOL] 17 ONE; BORON TRIFLUORIDE; STEROID; UNCLASSIFIED DRUG; BORANE DERIVATIVE; THIOL DERIVATIVE;

EID: 20544445931     PISSN: 0039128X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.steroids.2004.10.010     Document Type: Article
Times cited : (3)

References (15)
  • 2
    • 27644555825 scopus 로고
    • An efficient synthesis of estrone and 19-norsteroids from cholesterol
    • Sih CJ, Lee SS, Tsong YY, Wang KC, Chang FN. An efficient synthesis of estrone and 19-norsteroids from cholesterol. J Am Chem Soc 1965;87:2765-6.
    • (1965) J Am Chem Soc , vol.87 , pp. 2765-2766
    • Sih, C.J.1    Lee, S.S.2    Tsong, Y.Y.3    Wang, K.C.4    Chang, F.N.5
  • 3
    • 0002786379 scopus 로고
    • A new route to estrone from sterols
    • Sih CJ, Wang KC. A new route to estrone from sterols. J Am Chem Soc 1965;87:1387-8.
    • (1965) J Am Chem Soc , vol.87 , pp. 1387-1388
    • Sih, C.J.1    Wang, K.C.2
  • 5
    • 0018088560 scopus 로고
    • Synthesis and biochemical evaluation of inhibitors of estrogen biosynthesis
    • Brueggemeier RW, Flogel EE, Counsell RE. Synthesis and biochemical evaluation of inhibitors of estrogen biosynthesis. J Med Chem 1978;21:1007-11.
    • (1978) J Med Chem , vol.21 , pp. 1007-1011
    • Brueggemeier, R.W.1    Flogel, E.E.2    Counsell, R.E.3
  • 6
    • 84986707579 scopus 로고
    • Zur regioselektivität SH-haltiger nucleophile gegenüber androsta-1,4-dien-3,17-dion, einem vorläufer für biologisch active steroide
    • Müller A, Weiß D, Beckert R. Zur Regioselektivität SH-haltiger Nucleophile gegenüber androsta-1,4-dien-3,17-dion, einem Vorläufer für biologisch active steroide. Liebigs Ann Chem 1993:11-5.
    • (1993) Liebigs Ann Chem , pp. 11-15
    • Müller, A.1    Weiß, D.2    Beckert, R.3
  • 7
    • 0000635979 scopus 로고
    • Synthesis and structure of steroidal pregn-4-eno- and 5-pregnano[3,2-c]-pyrazoles. A novel class of potent anti-inflammatory steroids
    • Hirschmann R, Buchschacher P, Steinberg NG, Fried JH, Ellis R, Kent GJ, et al. Synthesis and structure of steroidal pregn-4-eno- and 5-pregnano[3,2-c]-pyrazoles. A novel class of potent anti-inflammatory steroids. J Am Chem Soc 1964;86:1520-7.
    • (1964) J Am Chem Soc , vol.86 , pp. 1520-1527
    • Hirschmann, R.1    Buchschacher, P.2    Steinberg, N.G.3    Fried, J.H.4    Ellis, R.5    Kent, G.J.6
  • 8
    • 0029963037 scopus 로고    scopus 로고
    • Synthesis and biological activity of azasteroidal[3,2-c]- And [17,16-c]pyrazoles
    • Gupta R, Pathak D, Jindal DP. Synthesis and biological activity of azasteroidal[3,2-c]- and [17,16-c]pyrazoles. Eur J Med Chem 1996;31:241-7.
    • (1996) Eur J Med Chem , vol.31 , pp. 241-247
    • Gupta, R.1    Pathak, D.2    Jindal, D.P.3
  • 10
    • 4243402811 scopus 로고
    • Synthesis of protein assimilating hormone, 17-Hydroxyl-17- methylandrostane[3,2-c]pyrazole
    • Wang S, Xie F, Song K. Synthesis of protein assimilating hormone, 17-Hydroxyl-17-methylandrostane[3,2-c]pyrazole. Chem Abstr 1993;119:203669y.
    • (1993) Chem Abstr , vol.119
    • Wang, S.1    Xie, F.2    Song, K.3
  • 11
    • 0001765088 scopus 로고
    • Synthesis and structure of steroidal 4-pregneno[3,2-c]pyrazoles. A novel class of potent anti-inflammatory steroids
    • Hirschmann R, Steinberg NG, Buschacher P, Fried JH, Kent GJ, Tishler M. Synthesis and structure of steroidal 4-pregneno[3,2-c]pyrazoles. A novel class of potent anti-inflammatory steroids. J Am Chem Soc 1963;85:120-2.
    • (1963) J Am Chem Soc , vol.85 , pp. 120-122
    • Hirschmann, R.1    Steinberg, N.G.2    Buschacher, P.3    Fried, J.H.4    Kent, G.J.5    Tishler, M.6
  • 14
    • 0029740419 scopus 로고    scopus 로고
    • Steroidal oxazoles, oxazolines, and oxazolidines
    • Camoutsis C. Steroidal oxazoles, oxazolines, and oxazolidines. J Heterocycl Chem 1996;33:539-57.
    • (1996) J Heterocycl Chem , vol.33 , pp. 539-557
    • Camoutsis, C.1
  • 15
    • 0028021230 scopus 로고
    • Synthesis of steroidal D-ring fused pyrazolines: Study of regiochemistry of addition
    • Green B, Sheu K. Synthesis of steroidal D-ring fused pyrazolines: study of regiochemistry of addition. Steroids 1994;59:479-80.
    • (1994) Steroids , vol.59 , pp. 479-480
    • Green, B.1    Sheu, K.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.