104770-12-9Relevant academic research and scientific papers
Synthesis of novel functionalized cispentacins through C-C oxidative cleavage of diendo-norbornene β-amino acid
Cherepanova, Maria,Kiss, Lorand,Sillanpaeae, Reijo,Fueloep, Ferenc
, p. 9757 - 9763 (2013/09/02)
Difunctionalized cispentacin derivatives with two new stereogenic centres have been synthesized from a diendo-norbornene β-amino acid in a stereocontrolled route, involving C-C double bond functionalization by dihydroxylation, followed by oxidative ring cleavage and transformation of the dialdehyde intermediates through a Wittig reaction.
STEREOCHEMICAL STUDIES 87; SATURATED HETEROCYCLES 82; SYNTHESIS AND STERIC STRUCTURE OF STEREOISOMERIC N-SUBSTITUTED TETRAHYDRO-1,3-OXAZINES FUSED WITH NORBORNANE OR NORBORNENE
Fueloep, Ferenc,Stajer, Geza,Bernath, Gabor,Sohar, Pal
, p. 5159 - 5168 (2007/10/02)
diendo- and diexo-2-Methylamino and 2-benzylamino-3-hydroxymethylbicycloheptanes and the corresponding bicycloheptenes (5a-d, 7a-d) were synthesized from β-amino acid esters containing the norbornane or norbornene skeleton (3a-d).The aminoal
