Zobrazeno 1 - 10
of 72
pro vyhledávání: '"U. Kerb"'
Autor:
A. Langemann, Andre Furlenmeier, U. Kerb, Guy Waldvogel, Andor Furst, Rudolf Prof Wiechert, P. Hocks
Publikováno v:
Helvetica Chimica Acta. 50:2387-2396
A synthesis of ecdysone is described by which the insect moulting hormone can be readily prepared. Oxidation of ergosterol gave the 6-keto-Δ7-function, and preparation of the Δ2-olefine followed by stereospecific hydroxylation led to the 2β,3β-gl
Autor:
U. Kerb, Guy Waldvogel, A. Langemann, Andre Furlenmeier, Rudolf Prof Wiechert, Andor Furst, P. Hocks
Publikováno v:
Helvetica Chimica Acta. 49:1581-1591
Experiments towards a synthesis of ecdysone (1) ([22R]-2β, 3β, 14, 22, 25-pentahydroxy-5β, 14α-cholest-7-en-6-one) have led to 2β, 3β-dihydroxy-6-keto-5α-steroids. These could be epimerized to the corresponding 5β-series. The proposed configu
Publikováno v:
Tetrahedron Letters. 9:4281-4284
Zusammenfassung Rubrosterone, a steroid with the ecdysone-skeleton recently isolated from the plant Achyranthes rubrofusca Wight , was synthesized from readily available starting material.
Autor:
Andor Furst, Rudolf Prof Wiechert, P. Hocks, Guy Waldvogel, U. Kerb, A. Langemann, Andre Furlenmeier
Publikováno v:
Helvetica Chimica Acta. 49:1591-1601
Publikováno v:
Tetrahedron. 21:1625-1634
A detailed NMR analysis of epimeric pairs of 1-methylated steroids in the A/B cis and Δ4-series has confirmed earlier configurational assignments. One-methyl steroids in the A/B trans series and the 1-methyl hydrocortisone synthesized therefrom are
Publikováno v:
Tetrahedron Letters. 9:4277-4280
Zusammenfassung A synthesis of crustecdysone, an insect and crustacean moulting hormone, is described in 19 stages starting from progesterone. The key intermediate is 2β, 3β-diacetoxy-5α-pregn-7-ene-6,20-dione.
Autor:
Rudolf Wiechert, A. Langemann, U. Kerb, Andor Furst, Guy Waldvogel, P. Hocks, Andre Furlenmeier
Publikováno v:
Tetrahedron Letters. 7:1387-1391
Autor:
Guy Waldvogel, U. Kerb, Andor Furst, P. Hocks, A. Langemann, Andre Furlenmeier, Rudolf Prof Wiechert, G. Schulz
Publikováno v:
Helvetica Chimica Acta. 49:1601-1606
Ecdysone (9), a hormone responsible for the skin shedding process of arthropoda, has been synthesized. (20S)-2β,3β-Diacetoxy-20-formyl-5β-pregn-7-en-6-one was prepared from the corresponding carboxylic acid and converted into ecdysone by a GRIGNAR
Publikováno v:
Tetrahedron Letters. 11:641-643
Autor:
U. Kerb, Paul Buchschacher, Mario Müller, Andre Furlenmeier, Rudolf Prof Wiechert, Ulrich Eder, Andor Furst, H. D. Berndt
Publikováno v:
Experientia. 27:759-761
The synthesis of 3β-acetoxy-16β, 20β-dihydroxy-4′-methyl-18-nor-5β, 14β-pregnano[13,14-f]hexahydro-1′, 4′-oxazepin-3′-one (20a) is described.