Search research articles
Contact Us
Filters
Showing results (1-10 of 24) with videos related to
Page
of 3
Sort By:
Die Pharmazie
|
May 1, 1979
[The development of a new highly potent progestagen, STS 557 (17 alpha-cyanomethyl-17 beta-hydroxy-13 beta-methylgona-4,9-dien-3-one) (proceedings)]
K Ponsold
Chemische Berichte
|
January 1, 1972
[Steroids. 32. Stereospecific preparation of nitrogen-containing steroids from aziridines and vicinal azidoalcohol mesylates]
K Ponsold, D Klemm
Tetrahedron Letters
|
March 1, 1970
[The addition of cyanamid and halogen to olefins. A new method for the preparation of vicinal halogencyanamines and aziridines]
K Ponsold, W Ihn
Experimental and Clinical Endocrinology
|
February 1, 1983
The synthetic approach to STS 557 - structure activity relationships in 17 alpha-CH2X-substituted 19-nortestosterone derivatives
M Hübner, K Ponsold
Chemische Berichte
|
January 1, 1971
[Steroids 28. Preparation of steroid hormone analogs from 2,3 beta-imino-5 alpha-androstan-17 beta-ol and 2 beta-amino-3 alpha-chlor-5 alpha-androstan-17 beta-ol]
K Ponsold, W Preibsch
Die Pharmazie
|
October 1, 1977
[Quantitative structure-activity relationship between physicochemical parameteters of 16alpha hetero substituted estradiols and the binding capacity to receptors of the rat uterus in vitro. 49]
K Ponsold, J Draffehn, B Schönecker
Journal of Steroid Biochemistry
|
October 1, 1984
Quantitative structure-activity relationships of cardiotonic steroids using empirical molecular electrostatic potentials and semiempirical molecular orbital calculations
M Bohl, K Ponsold, G Reck
Die Pharmazie
|
January 1, 1976
[Conversion of 15 beta.16 beta-epoxy-3-methoxyestra-1.3.5(10)-triene-17-one using hydroxylamine derivatives. 43. Steroids]
K Ponsold, G Schubert, W Ihn
Experimental and Clinical Endocrinology
|
February 1, 1983
Preclinical data on STS 557. Introduction
K Schubert, K Ponsold, M Oettel
Die Pharmazie
|
January 1, 1975
[16-alpha-heterosubstituted estradiols (estradiol analogs). Preparation and binding power at receptors of rat uterus in vitro]
K Ponsold, J Schlegel, B Schönecker, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 24) with videos related to
Sort By:
Page
of 3
Die Pharmazie
|
May 1, 1979
[The development of a new highly potent progestagen, STS 557 (17 alpha-cyanomethyl-17 beta-hydroxy-13 beta-methylgona-4,9-dien-3-one) (proceedings)]
K Ponsold
Chemische Berichte
|
January 1, 1972
[Steroids. 32. Stereospecific preparation of nitrogen-containing steroids from aziridines and vicinal azidoalcohol mesylates]
K Ponsold, D Klemm
Tetrahedron Letters
|
March 1, 1970
[The addition of cyanamid and halogen to olefins. A new method for the preparation of vicinal halogencyanamines and aziridines]
K Ponsold, W Ihn
Experimental and Clinical Endocrinology
|
February 1, 1983
The synthetic approach to STS 557 - structure activity relationships in 17 alpha-CH2X-substituted 19-nortestosterone derivatives
M Hübner, K Ponsold
Chemische Berichte
|
January 1, 1971
[Steroids 28. Preparation of steroid hormone analogs from 2,3 beta-imino-5 alpha-androstan-17 beta-ol and 2 beta-amino-3 alpha-chlor-5 alpha-androstan-17 beta-ol]
K Ponsold, W Preibsch
Die Pharmazie
|
October 1, 1977
[Quantitative structure-activity relationship between physicochemical parameteters of 16alpha hetero substituted estradiols and the binding capacity to receptors of the rat uterus in vitro. 49]
K Ponsold, J Draffehn, B Schönecker
Journal of Steroid Biochemistry
|
October 1, 1984
Quantitative structure-activity relationships of cardiotonic steroids using empirical molecular electrostatic potentials and semiempirical molecular orbital calculations
M Bohl, K Ponsold, G Reck
Die Pharmazie
|
January 1, 1976
[Conversion of 15 beta.16 beta-epoxy-3-methoxyestra-1.3.5(10)-triene-17-one using hydroxylamine derivatives. 43. Steroids]
K Ponsold, G Schubert, W Ihn
Experimental and Clinical Endocrinology
|
February 1, 1983
Preclinical data on STS 557. Introduction
K Schubert, K Ponsold, M Oettel
Die Pharmazie
|
January 1, 1975
[16-alpha-heterosubstituted estradiols (estradiol analogs). Preparation and binding power at receptors of rat uterus in vitro]
K Ponsold, J Schlegel, B Schönecker, et al.
Page
of 3