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Hyphenating the Curtius Rearrangement with Morita-Baylis-Hillman Adducts: Synthesis of Biologically Active Acyloins and Vicinal Aminoalcohols
(Soc Brasileira QuimicaSao PauloBrasil, 2011)
An alternative approach to aminodiols from Baylis-Hillman adducts. Stereoselective synthesis of chloramphenicol, fluoramphenicol and thiamphenicol
(Soc Brasileira QuimicaSao PauloBrasil, 2005)
An approach to substituted dihydroisoquinolin-1(2H)-ones from Baylis-Hillman adducts
(Pergamon-elsevier Science LtdOxfordInglaterra, 2003)
Diastereoselective Approach to Substituted Oxazolidinones from Morita-Baylis-Hillman Adducts
(Taylor & Francis IncPhiladelphiaEUA, 2011)
Acyloins from Morita-Baylis-Hillman adducts: an alternative approach to the racemic total synthesis of bupropion
(Pergamon-elsevier Science LtdOxfordInglaterra, 2008)
A practical amine-free synthesis of symmetric ureas and thioureas by self-condensation if iso(thio)cyanates
(Thieme Stuttgart, 1999)
Isocianates and isothiocyanates are readily transformed into the corresponding symmetric N,N'-disubstituted ureas and thioureas upon treatment with pyridine-water with no formation of side products. Evidence is shown for ...
Synthesis of 3-aminolactams as X-Gly constrained pseudodipeptides and conformational study of a Trp-Gly surrogate
(AMER CHEMICAL SOC, 2003-12-12)
3-Amino-delta-valerolactams trans-11a-c were synthesized through conjugate addition and Curtius rearrangement and converted into Fmoc-{Trp-Gly}, Fmoc-{Ile-Gly}, and Fmoc-{Phe-Gly} pseudo-dipeptides. Conformational analyses ...
An alternative approach to aminodiols from Baylis-Hillman adducts: stereoselective synthesis of chloramphenicol, fluoramphenicol and thiamphenicol
(Sociedade Brasileira de Química, 2005)