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Caselli, AS, Collins, DJ, Stone, GM (1982) The structure and function of oestrogens. III. 3,17β-Dihydroxy-6-oxaoestra-1,3,5(10),8(9)-tetraen-7-one and related steroidal coumarins. Australian Journal of Chemistry, 35 (4). 799pp. doi:10.1071/ch9820799

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Reference TypeJournal (article/letter/editorial)
TitleThe structure and function of oestrogens. III. 3,17β-Dihydroxy-6-oxaoestra-1,3,5(10),8(9)-tetraen-7-one and related steroidal coumarins
JournalAustralian Journal of Chemistry
AuthorsCaselli, ASAuthor
Collins, DJAuthor
Stone, GMAuthor
Year1982Volume35
Issue4
PublisherCSIRO Publishing
DOIdoi:10.1071/ch9820799Search in ResearchGate
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Mindat Ref. ID8384857Long-form Identifiermindat:1:5:8384857:7
GUID0
Full ReferenceCaselli, AS, Collins, DJ, Stone, GM (1982) The structure and function of oestrogens. III. 3,17β-Dihydroxy-6-oxaoestra-1,3,5(10),8(9)-tetraen-7-one and related steroidal coumarins. Australian Journal of Chemistry, 35 (4). 799pp. doi:10.1071/ch9820799
Plain TextCaselli, AS, Collins, DJ, Stone, GM (1982) The structure and function of oestrogens. III. 3,17β-Dihydroxy-6-oxaoestra-1,3,5(10),8(9)-tetraen-7-one and related steroidal coumarins. Australian Journal of Chemistry, 35 (4). 799pp. doi:10.1071/ch9820799
In(1982) Australian Journal of Chemistry Vol. 35 (4) CSIRO Publishing

See Also

These are possibly similar items as determined by title/reference text matching only.

CASELLI, A. S., COLLINS, D. J., STONE, G. M. (1982) ChemInform Abstract: THE STRUCTURE AND FUNCTION OF ESTROGENS. III. 3,17β-DIHYDROXY-6-OXAESTRA-1,3,5(10),8-TETRAEN-7-ONE AND RELATED STEROIDAL COUMARINS. Chemischer Informationsdienst, 13 (35) doi:10.1002/chin.198235293
Collins, DJ, Matthews, WA, Stone, GM (1979) The Structure and Function of Oestrogens. II. The Synthesis and Oestrogenic Activity of 4b-Methyl 4b,5,6,12-tetrahydrochrysene-2,8-diol and 4b-Methyl-cis-4b,5,6,10b,11,12-hexahydrochrysene-2,8-diol and Related Compounds. Australian Journal of Chemistry, 32 (5). 1107pp. doi:10.1071/ch9791107
Collins, DJ (1983) The structure and function of oestrogens. V. Synthesis of (9,12,12-2H3)- and (11ζ 12,12-2H3)-oestradiol. Australian Journal of Chemistry, 36 (2). 403pp. doi:10.1071/ch9830403
Collins, DJ, Cullen, JD, Stone, GM (1988) The Structure and Function of Estrogens .10. Synthesis of 5,5-Dimethyl-Cis-4b,5,6,10b,11,12-Hexahydrochrysene-2,8-Diol - the Estrogenic Activity of This and of Related C-Methylated Hydrochrysenediols. Australian Journal of Chemistry, 41 (5). 745pp. doi:10.1071/ch9880745
Collins, DJ, Sjovall, J (1983) The structure and function of oestrogens. IV. Synthesis of 17α-ethynyloestradiol specifically polydeuterated in ring C. Australian Journal of Chemistry, 36 (2). 339pp. doi:10.1071/ch9830339
Findlay, John A., Mebe, Paul, Stern, Michael D., Givner, M. L. (1980) Total synthesis of 3,17β-dihydroxy-6-oxaestra-1,3,5(10),7-tetraen and related miroestrol analogues. Canadian Journal of Chemistry, 58 (14). 1427-1434 doi:10.1139/v80-224
Collins, DJ, Matthews, WA (1979) The Structure and Function of Oestrogens. I. Synthesis of 4b-Methyl-trans-4b,5,6,10b,11,12-hexahydrochrysene-2,8-diol. Australian Journal of Chemistry, 32 (5). 1093pp. doi:10.1071/ch9791093
Burge, GL, Collins, DJ, Reitze, JD (1982) Synthesis of 3-Ethenyl-4-methylcyclohex-2-en-1-one from 4-methylanisole. Australian Journal of Chemistry, 35 (9). 1913pp. doi:10.1071/ch9821913
Collins, DJ, Cullen, JD, Fallon, GD, Gatehouse, BM (1984) The structure and function of oestrogens. VIII. Synthesis of 5,5, 10b-Trimethyl-cis-4b,5,6,10b,11,12-hexahydrochrysene-2,8-diol from 6-Methoxy-3,4-dihydronaphthalen-1(2H)-one. Australian Journal of Chemistry, 37 (11). 2279pp. doi:10.1071/ch9842279
Collins, DJ, Jhingran, AG, Rutschmann, SB (1989) Enolic Ortho Esters. IV. Synthesis of the 8-α and 8-β Epimers of a 6-Oxa Steroidal Enolic Ortho Ester. Australian Journal of Chemistry, 42 (10). 1769pp. doi:10.1071/ch9891769
Collins, DJ, Fallon, GD, Skene, CE (1992) The Structure and Function of Estrogens. XI. Synthesis of (±)-7(8→11α)abeo-Estradiol and Its 9,11-Didehydro Derivative. Australian Journal of Chemistry, 45 (1). 71pp. doi:10.1071/ch9920071
 
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