NO129226B - - Google Patents

Download PDF

Info

Publication number
NO129226B
NO129226B NO14693562A NO14693562A NO129226B NO 129226 B NO129226 B NO 129226B NO 14693562 A NO14693562 A NO 14693562A NO 14693562 A NO14693562 A NO 14693562A NO 129226 B NO129226 B NO 129226B
Authority
NO
Norway
Prior art keywords
solution
pregnene
dimethyl
dioxy
methyl
Prior art date
Application number
NO14693562A
Other languages
English (en)
Norwegian (no)
Inventor
R Oberman
A Snijders
Original Assignee
Philips Usfa Nv
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Philips Usfa Nv filed Critical Philips Usfa Nv
Publication of NO129226B publication Critical patent/NO129226B/no

Links

Classifications

    • G—PHYSICS
    • G09—EDUCATION; CRYPTOGRAPHY; DISPLAY; ADVERTISING; SEALS
    • G09C—CIPHERING OR DECIPHERING APPARATUS FOR CRYPTOGRAPHIC OR OTHER PURPOSES INVOLVING THE NEED FOR SECRECY
    • G09C1/00—Apparatus or methods whereby a given sequence of signs, e.g. an intelligible text, is transformed into an unintelligible sequence of signs by transposing the signs or groups of signs or by replacing them by others according to a predetermined system
    • G09C1/06—Apparatus or methods whereby a given sequence of signs, e.g. an intelligible text, is transformed into an unintelligible sequence of signs by transposing the signs or groups of signs or by replacing them by others according to a predetermined system wherein elements corresponding to the signs making up the clear text are operatively connected with elements corresponding to the signs making up the ciphered text, the connections, during operation of the apparatus, being automatically and continuously permuted by a coding or key member

Landscapes

  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Engineering & Computer Science (AREA)
  • Theoretical Computer Science (AREA)
  • Control Of Stepping Motors (AREA)
  • Steroid Compounds (AREA)
NO14693562A 1961-12-29 1962-12-22 NO129226B (enExample)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
NL273047 1961-12-29

Publications (1)

Publication Number Publication Date
NO129226B true NO129226B (enExample) 1974-03-11

Family

ID=19753506

Family Applications (1)

Application Number Title Priority Date Filing Date
NO14693562A NO129226B (enExample) 1961-12-29 1962-12-22

Country Status (5)

Country Link
DK (1) DK564262A (enExample)
FR (1) FR1584201A (enExample)
GB (1) GB1120031A (enExample)
NL (2) NL105818C (enExample)
NO (1) NO129226B (enExample)

Also Published As

Publication number Publication date
NL105818C (enExample)
FR1584201A (enExample) 1969-12-19
GB1120031A (en) 1968-07-17
NL273047A (enExample)
DK564262A (da) 1982-04-28

Similar Documents

Publication Publication Date Title
US2945852A (en) 17-oxygenated 9alpha-substituted androstano [3, 2-c] pyrazoles and derivatives
US3170934A (en) Unsaturated 19-oxygenated 3-oxosteroids and process for their manufacture
US3032552A (en) 1-methyl steroids of the androstane series
US3639392A (en) Cardioactive oxido-bufatrienolides
US2715621A (en) Steroids
US2673867A (en) 2, 17 alpha-dioxy-3, 11, 20-triketoallopregnanes and process
NO129226B (enExample)
US3096350A (en) 6, 16alpha-dimethyl-delta1, 4, 6-pregnatriene-17alpha-ol-3, 20-dione and esters thereof
US2985652A (en) 3-enol esters of 6-halo-16alpha-hydroxy cortical hormones
US2562030A (en) Production of 17-hydroxy 20-keto steroid compounds
US3032565A (en) Process for the manufacture of 6-alkoxy-and 6-keto steroids and compounds obtained thereby
US3254098A (en) Process for the production of 19 norandrostanes and 19 nor-pregnanes
US3100204A (en) Haloethisterone compounds
US3684674A (en) Process for preparing 18-cyano-pregnane compounds
US3040035A (en) 17alpha-acyloxy-6alpha-methyl-16-methylenepregn-4-ene-3, 20-diones and process and intermediates for the preparation thereof
US3080381A (en) Optionally 6-methylated and optionally 17-alkanoyloxygenated 2-oxapregnane-3, 20-diones, a-homo compounds corresponding, and 4, 5-dehydro and 4, 5; 6, 7-bisdehydro derivatives thereof
US3182075A (en) 17-substituted 19-norpregna-1, 3, 5(10), 6, 8-pentaen-20-ones
US2935511A (en) Process of preparing 11 beta-hydroxy steroids
NO132391B (enExample)
Pike et al. Addition of Alkyl Vinyl Ethers to Δ16-20-Keto Steroids. II1
US3062845A (en) Process for the conversion of alpha-acetyl steroids to beta-acetyl steroids and intermediates therein
Hesse et al. Substitution at Unactivated Carbon. The Synthesis of 18-and 19-Substituted Derivatives of 11β-Hydroxyprogesterone*, 1, 2
US3057858A (en) 6alpha-substituted-16beta-methyl-11-epihydrocortisone
US2791585A (en) Steroid alpha-halo ketals
US3579543A (en) Delta**1,3,5(10)-2- (or 4-)formyl-3-hydroxyoestratriene compounds