Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Przemysław Bazydło"'
Autor:
Agnieszka Wojtkielewicz, Damian Pawelski, Przemysław Bazydło, Aneta Baj, Stanisław Witkowski, Jacek W. Morzycki
Publikováno v:
Molecules, Vol 25, Iss 10, p 2377 (2020)
A concise synthesis of (16S,20S)-3β-hydroxy-5α-pregnane-20,16-carbolactam from tigogenin via the corresponding lactone is described. The most efficient synthetic route consisted of the lactone ring-opening with aminoalane reagent followed by PDC or
Externí odkaz:
https://doaj.org/article/fe2851da240e46f0b6c87cf95e2805df
Autor:
Agnieszka Hryniewicka, Barbara Seroka, Ewelina Dudź, Przemysław Bazydło, Agnieszka Wojtkielewicz, Jacek W. Morzycki, Zenon Łotowski
Publikováno v:
Steroids. 147:19-27
Two series of cholestane-based diamines (1,2 and 1,3) were synthesized using simple and efficient procedures. The convenient substrates for these syntheses were cholesteryl mesylate and tosylate, which were converted to appropriate amines via easily
Autor:
Damian Pawelski, Aneta Baj, Przemysław Bazydło, Jacek W. Morzycki, Agnieszka Wojtkielewicz, Stanisław Witkowski
Publikováno v:
Molecules
Volume 25
Issue 10
Molecules, Vol 25, Iss 2377, p 2377 (2020)
Volume 25
Issue 10
Molecules, Vol 25, Iss 2377, p 2377 (2020)
A concise synthesis of (16S,20S)-3&beta
hydroxy-5&alpha
pregnane-20,16-carbolactam from tigogenin via the corresponding lactone is described. The most efficient synthetic route consisted of the lactone ring-opening with aminoalane reagent f
hydroxy-5&alpha
pregnane-20,16-carbolactam from tigogenin via the corresponding lactone is described. The most efficient synthetic route consisted of the lactone ring-opening with aminoalane reagent f