104770-18-5Relevant articles and documents
Stereocontrolled one-step synthesis of difunctionalised cispentacin derivatives through ring-opening metathesis of norbornene β-amino acids
Kiss, Lornd,Kardos, Mrton,Forr, Eniko,Fül?p, Ferenc
, p. 1283 - 1289 (2015/03/04)
Through the ring-opening metathesis of norbornene or oxanorbornene β-amino acids with ethylene in the presence of certain Ru catalysts, a facile and convenient stereocontrolled one-step method was devised for the preparation of divinylated cispentacins an
Stereochemical Studies, 106. - Saturated Heterocycles, 110. - Synthesis of Methylene-bridged Partially Saturated Quinazolones
Stajer, Geza,Szabo, Angela E.,Fueloep, Ferenc,Bernath, Gabor,Sohar, Pal
, p. 259 - 264 (2007/10/02)
With imidates, esters (5-8) of di-endo (1 and 2) and di-exo (3 and 4) norbornane- and norbornene-β-amino acids yield methylene-bridged tetrahydro- (18 and 20) and hexahydro-4-quinazolinones (17 and 19); the reaction of the corresponding carboxamides (9-12
Stereochemical Studies. 81 . Saturated Heterocycles. 69 . Preparation of Methylene-bridged 3,1-Benzoxazines, 3,1-Benzoxazin-2-ones and 3,1-Benzoxazine-2-thiones
Stajer, Geza,Szabo, Angela E.,Fueloep, Ferenc,Bernath, Gabor,Sohar, Pal
, p. 1373 - 1376 (2007/10/02)
3-exo-Aminobicyclohept-5-ene-2-exo-carboxylic acid and ethyl 3-endo-aminobicycloheptane-2-endo-carboxylate (6) were reduced with lithium aluminum hydride to the corresponding bicyclic aminoalcohols 3 and 4.These and the saturated endo-endo a