Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

E R Jones

Showing results (51-60 of 70) with videos related to

Pageof 7
Sort By:
Microbial Ecology|July 30, 2005
Biogenic stabilization of intertidal sediments: the importance of extracellular polymeric substances produced by benthic diatomsJ F C de Brouwer, K Wolfstein, G K Ruddy, et al.
Journal of the Chemical Society. Perkin Transactions 1|January 1, 1972
Studies in the steroid group. 83. 1-, 2-, 3-, 4-, 6-, 12-, 15-, and 16-monohydroxy-5 -androstanes and their derivativesI M Clark, A S Clegg, W A Denny, et al.
Journal of the Chemical Society. Perkin Transactions 1|January 1, 1972
Studies in the steroid group. LXXXIV. Preparation and reactions of 15-oxygenated androstanesI M Clark, W A Denny, E R Jones, et al.
Journal of the Chemical Society. Perkin Transactions 1|January 1, 1972
Studies in in the steroid group. LXXXII. The preparation of nine mono- and eight di-oxoandrostanes, 5 -estran-17-one, and 5 -pregnane-2,20-dioneA S Clegg, W A Denny, E R Jones, et al.
Journal of the Chemical Society. Perkin Transactions 1|January 1, 1974
Microbiological hydroxylation of steroids. XI. Convenient routes to 3,7-, 3,11-, 3,12-, 7,11-, 7,17-, and 11,17-dioxygenated 5 alpha-androstanes and to 5 alpha-androstan-11-oneA M Bell, V E Chambers, E R Jones, et al.
Journal of the Chemical Society. Perkin Transactions 1|January 1, 1975
Microbiological hydroxylation. Part XVII. Introduction of 16alpha-, 9alpha-, and 3alpha-hydroxy-groups into dioxygenated 5alpha-androstanes by the fungus Diaporthe celastrinaA M Bell, A D Boul, E R Jones, et al.
Journal of the Chemical Society. Perkin Transactions 1|January 1, 1972
Microbiological hydroxylation of steroids. VI. Hydroxylation of simple mono- and di-oxygenated 5 -androstanes and of 3-oxoestranes with the fungus Aspergillus ochraceusA M Bell, J W Browne, W A Denny, et al.
Journal of the Chemical Society. Perkin Transactions 1|January 1, 1973
Microbiological hydroxylation of steroids. VII. The pattern of dihydroxylation of mono-oxo-5 alpha-androstanes and 5 alpha-estranes with the fungus Rhizopus nigricansJ W Browne, W A Denny, E R Jones, et al.
Journal of the Chemical Society. Perkin Transactions 1|January 1, 1971
Microbiological hydroxylation of steroids. 3. A convenient, microbiological route to 15-oxygenated 5-alpha-androstanesJ W Blunt, I M Clark, J M Evans, et al.
Journal of the Chemical Society. Perkin Transactions 1|January 1, 1973
Microbiological hydroxylation of steroids. IX. Hydroxylation of diketones and keto-alcohols derived from 5 alpha-androstane with the fungi Rhizopus arrhizus and Rhizopus circinnans. Steroidal 18- and 19-proton magnetic resonance signalsA M Bell, I M Clark, W A Denny, et al.
Pageof 7

Showing results (51-60 of 70) with videos related to

Sort By:
Pageof 7
Microbial Ecology|July 30, 2005
Biogenic stabilization of intertidal sediments: the importance of extracellular polymeric substances produced by benthic diatomsJ F C de Brouwer, K Wolfstein, G K Ruddy, et al.
Journal of the Chemical Society. Perkin Transactions 1|January 1, 1972
Studies in the steroid group. 83. 1-, 2-, 3-, 4-, 6-, 12-, 15-, and 16-monohydroxy-5 -androstanes and their derivativesI M Clark, A S Clegg, W A Denny, et al.
Journal of the Chemical Society. Perkin Transactions 1|January 1, 1972
Studies in the steroid group. LXXXIV. Preparation and reactions of 15-oxygenated androstanesI M Clark, W A Denny, E R Jones, et al.
Journal of the Chemical Society. Perkin Transactions 1|January 1, 1972
Studies in in the steroid group. LXXXII. The preparation of nine mono- and eight di-oxoandrostanes, 5 -estran-17-one, and 5 -pregnane-2,20-dioneA S Clegg, W A Denny, E R Jones, et al.
Journal of the Chemical Society. Perkin Transactions 1|January 1, 1974
Microbiological hydroxylation of steroids. XI. Convenient routes to 3,7-, 3,11-, 3,12-, 7,11-, 7,17-, and 11,17-dioxygenated 5 alpha-androstanes and to 5 alpha-androstan-11-oneA M Bell, V E Chambers, E R Jones, et al.
Journal of the Chemical Society. Perkin Transactions 1|January 1, 1975
Microbiological hydroxylation. Part XVII. Introduction of 16alpha-, 9alpha-, and 3alpha-hydroxy-groups into dioxygenated 5alpha-androstanes by the fungus Diaporthe celastrinaA M Bell, A D Boul, E R Jones, et al.
Journal of the Chemical Society. Perkin Transactions 1|January 1, 1972
Microbiological hydroxylation of steroids. VI. Hydroxylation of simple mono- and di-oxygenated 5 -androstanes and of 3-oxoestranes with the fungus Aspergillus ochraceusA M Bell, J W Browne, W A Denny, et al.
Journal of the Chemical Society. Perkin Transactions 1|January 1, 1973
Microbiological hydroxylation of steroids. VII. The pattern of dihydroxylation of mono-oxo-5 alpha-androstanes and 5 alpha-estranes with the fungus Rhizopus nigricansJ W Browne, W A Denny, E R Jones, et al.
Journal of the Chemical Society. Perkin Transactions 1|January 1, 1971
Microbiological hydroxylation of steroids. 3. A convenient, microbiological route to 15-oxygenated 5-alpha-androstanesJ W Blunt, I M Clark, J M Evans, et al.
Journal of the Chemical Society. Perkin Transactions 1|January 1, 1973
Microbiological hydroxylation of steroids. IX. Hydroxylation of diketones and keto-alcohols derived from 5 alpha-androstane with the fungi Rhizopus arrhizus and Rhizopus circinnans. Steroidal 18- and 19-proton magnetic resonance signalsA M Bell, I M Clark, W A Denny, et al.
Pageof 7