Zobrazeno 1 - 10
of 27
pro vyhledávání: '"F. E. Carlon"'
Publikováno v:
Tetrahedron. 18:373-378
The synthesis of a number of 18-oxygenated steroids by means of photolysis of certain 20-nitrites is reported. These have been correlated with the Kurchi alkaloids, conessine and holarrhimine, and paravallarine.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13184e32c760675d4094b38eab253388
https://doi.org/10.1016/s0040-4020(01)93253-3
https://doi.org/10.1016/s0040-4020(01)93253-3
Publikováno v:
The Journal of Organic Chemistry. 33:1566-1570
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08ffdd953d0565917d3046a10d52f298
https://doi.org/10.1021/jo01268a057
https://doi.org/10.1021/jo01268a057
Autor:
M. L. Gilmore, Emanuel B Hershberg, A. L. Nussbaum, F. E. Carlon, Eugene P. Oliveto, William Charney, David H Gould
Publikováno v:
Journal of the American Chemical Society. 81:5230-5233
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17fa6bdcca664d44c4126df5b4a52587
https://doi.org/10.1021/ja01528a052
https://doi.org/10.1021/ja01528a052
Publikováno v:
Tetrahedron. 21:2509-2515
The photolytic rearrangement of the steroidal 3,5-cyclo-6-keto system to give the Δ 4 -6-keto system is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b384d286f1ca93f928fd74e88bb4e5f6
https://doi.org/10.1016/s0040-4020(01)93906-7
https://doi.org/10.1016/s0040-4020(01)93906-7
Autor:
A.L. Nussbaum, F. E. Carlon
Publikováno v:
Tetrahedron. 8:145-149
Structures are assigned to two pairs of geometrical isomers of steroidal Δ17(20) enol acetates, based on their conversion by catalytic hydrogenation to products of known stereochemistry. The structures of 17,20-epoxides derived from one of these iso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::70f68eafbd99b9632abd77c4c59e6127
https://doi.org/10.1016/s0040-4020(01)93340-x
https://doi.org/10.1016/s0040-4020(01)93340-x
Publikováno v:
The Journal of Organic Chemistry. 33:3695-3699
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41b9540d218a9c4409f7aff28c8fa14d
https://doi.org/10.1021/jo01274a004
https://doi.org/10.1021/jo01274a004
The synthesis of 6α,16α- and 6α,16β-dimethyl-9α, 11β-dichlobo-1,4-pregnadiene-1α,21-diol-5,20-diones
Publikováno v:
Steroids. 7:234-248
Synthetic schemes leading to the title compounds (XII and XXII) from 6,16-dimethyl-5,16-pregnadien-5β-ol-20-one acetate are described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e5addc63ad7ec901f2372b9eba2a0e8
https://doi.org/10.1016/0039-128x(66)90125-5
https://doi.org/10.1016/0039-128x(66)90125-5
Publikováno v:
Journal of Medicinal Chemistry. 14:33-35
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1860404792abec85a3c66cb980ce8fa
https://doi.org/10.1021/jm00283a008
https://doi.org/10.1021/jm00283a008
Publikováno v:
J. Chem. Soc. C. :1352-1354
The 17 α-hydroxy-16-methylene steroids (9a), (12), (13), (14), and (16) were converted into the corresponding 17α-acetoxy-17β-methyl-16-methylene-17a-oxo-D-homoandrostanes (10b), (1), (2), (15), and (17), respectively, by treatment with boron trif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::afd7497f2bc6faaa2f8086502471c751
https://doi.org/10.1039/j39700001352
https://doi.org/10.1039/j39700001352
Autor:
F. E. CARLON, R. W. DRAPER
Publikováno v:
Chemischer Informationsdienst. 15
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91cf7e2cd5fa1202c3d654b27fcef612
https://doi.org/10.1002/chin.198407296
https://doi.org/10.1002/chin.198407296