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Eignerová, L., Procházka, Ž. (1974) Resolution of racemic 3-methoxy-14α-hydroxy-D-homo-1,3,5(10)-estratrien-17a-one. Collection of Czechoslovak Chemical Communications, 39. 2828-2834 doi:10.1135/cccc19742828

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Reference TypeJournal (article/letter/editorial)
TitleResolution of racemic 3-methoxy-14α-hydroxy-D-homo-1,3,5(10)-estratrien-17a-one
JournalCollection of Czechoslovak Chemical Communications
AuthorsEignerová, L.Author
Procházka, Ž.Author
Year1974Volume39
PublisherInstitute of Organic Chemistry & Biochemistry
DOIdoi:10.1135/cccc19742828Search in ResearchGate
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Mindat Ref. ID4382547Long-form Identifiermindat:1:5:4382547:3
GUID0
Full ReferenceEignerová, L., Procházka, Ž. (1974) Resolution of racemic 3-methoxy-14α-hydroxy-D-homo-1,3,5(10)-estratrien-17a-one. Collection of Czechoslovak Chemical Communications, 39. 2828-2834 doi:10.1135/cccc19742828
Plain TextEignerová, L., Procházka, Ž. (1974) Resolution of racemic 3-methoxy-14α-hydroxy-D-homo-1,3,5(10)-estratrien-17a-one. Collection of Czechoslovak Chemical Communications, 39. 2828-2834 doi:10.1135/cccc19742828
In(1974) Collection of Czechoslovak Chemical Communications Vol. 39. Institute of Organic Chemistry & Biochemistry

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EIGNEROVA, L., PROCHAZKA, Z. (1974) ChemInform Abstract: STEROIDS PART 174, RESOLUTION OF RACEMIC 3-METHOXY-14ALPHA-HYDROXY-D-HOMO-1,3,5(10)-ESTRATRIEN-17A-ONE. Chemischer Informationsdienst, 5 (52) doi:10.1002/chin.197452449
Buděšínský, Miloš, Kasal, Alexander, Procházka, Želimír, Thoa, Huynh Kim, Vašíčková, Soňa, Kočovský, Pavel (1991) Revision of the structure of 3-methoxy-14α-hydroxy-D-homo-1,3,5-(10)-estratrien-17a-one. A simple 1H NMR method for the determination of configuration of hydroxy group in position 5 and/or 14 of the D-homo-steroid skeleton. Collection of Czechoslovak Chemical Communications, 56. 1512-1524 doi:10.1135/cccc19911512
Eignerová, L., Procházka, Ž. (1974) Biological transformation of 17α,21-dihydroxy-4-pregnene-3,20-dione with fruit-body slices of some mushrooms. Collection of Czechoslovak Chemical Communications, 39. 307-309 doi:10.1135/cccc19740307
Procházka, Ž., Buděšínský, M., Prekajski, P. (1974) Microbial oxygenation of 6β-hydroxy-3α,5-cyclo-5α-androstan-17-one with Rhizopus nigricans. Collection of Czechoslovak Chemical Communications, 39. 982-992 doi:10.1135/cccc19740982
Kočovský, P., Procházka, Ž. (1974) The synthesis of androstane derivatives with an aromatic B-ring. Collection of Czechoslovak Chemical Communications, 39. 1905-1913 doi:10.1135/cccc19741905
Procházka, Ž. (1959) Isolation of sulforaphane from hoary cress (Lepidium draba L.). Collection of Czechoslovak Chemical Communications, 24. 2429-2430 doi:10.1135/cccc19592429
Uchytil, B., Procházka, M. (1974) Chloro- and methoxybutenonitriles. Collection of Czechoslovak Chemical Communications, 39. 2951-2960 doi:10.1135/cccc19742951
Procházka, Ž., Šanda, V., Jirousek, L. (1959) Isothiocyanate im wirsing- und rosenkohl. Collection of Czechoslovak Chemical Communications, 24. 3606-3610 doi:10.1135/cccc19593606
Constantzas, N., Procházka, Ž., Jindra, A. (1959) The reaction of 3-indolylpyruvic acid with L-ascorbic acid. Collection of Czechoslovak Chemical Communications, 24. 1702-1703 doi:10.1135/cccc19591702
Thoa, Huynh Kim, Šašek, Václav, Buděšínský, Miloš, Jablonský, Ivan, Eignerová, Ludmila, Chan, Nguyen Gia, Procházka, Želimír (1978) Biological transformation of 3β-hydroxy-5-androsten-17-one with the mushroom Pleurotus ostreatus (JACQ. ex FR.) KUMM. Collection of Czechoslovak Chemical Communications, 43. 336-343 doi:10.1135/cccc19780336
Kašpar, M., Procházka, M. (1974) Pyrolyses of substituted acetyloxy compounds. Collection of Czechoslovak Chemical Communications, 39. 3124-3130 doi:10.1135/cccc19743124
 
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