1034089-14-9Relevant academic research and scientific papers
Diastereoselective addition of allyl reagents to variously N-monoprotected and N,N-diprotected L-alaninals
Gryko, Dorota,Jurczak, Janusz
, p. 2705 - 2711 (2000)
Diastereoselective C3-elongation processes of N-Boc-, N-Z-, N-Bn-N-Boc-, and N-Bn-N-Z-L-alaninals (Boc = 'BuOCO, Z = PhCH2OCO, Bn = PhCH2) using various allyl reagents, such as allyl bromide in the presence of Zn/aqueous N
PYRIMIDINE CARBOXAMIDES AS GSK-3 INHIBITORS
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Page/Page column 32, (2018/06/12)
The disclosure generally relates to compounds of formula I, including their salts, as well as compositions and methods of using the compounds to treat disorders associated with GSK-3.
A facile access to pyrroles from amino acids via an aza-Wacker cyclization
Zhang, Zuhui,Zhang, Jintang,Tan, Jiajing,Wang, Zhiyong
, p. 5180 - 5182 (2008/12/20)
(Chemical Equation Presented) A facile and efficient synthesis of pyrroles from readily available amino acids is described. The key step in the method is an aza-Wacker oxidative cyclization catalyzed by palladium(II)/Cu(OTf) 2. A series of pyrroles were obtained by this method under mild conditions.
CrCl2 mediated addition of allylic halides or phosphates to N-protected α-amino aldehydes. Stereocontrolled synthesis of a new core for C2 symmetric HIV-protease inhibitors
Ciapetti, Paola,Falorni, Massimo,Taddei, Maurizio
, p. 7379 - 7390 (2007/10/03)
The addition of γ-monosubstituted allylchromium(III) reagents to N-protected α-amino aldehydes proceeds in a stereoconvergent manner in contrast with the case of the unsubstituted reagents, where the stereoselectivity depends on the nature of the group bo
