Synthesis of 3,4-Dihydropyrimidin-2(1H)-one-5-carboxamides Mousa Soleymani and Hamid Reza Memarian

When this reaction was car- ried out over various acid catalysts the yield and rate of the reaction were increased.. Using Zn 2+ supported on montmorillonite-KSF as catalyst led

A series of previously unknown pyrimidin-2(1H)-ones containing chiral amino acid fragments was synthesized from 1,1,3,3-tetramethoxypropane and N-carbamoyl derivatives of amino

A one-pot synthesis of dialkyl 2-(diphenoxyphosphoryl)-3-[hydroxy (alkyl)(aryl) sulfanyl] succi- nate derivatives via the reaction between dialkyl acetylenedicarboxylates,

After N-galactosylation and subsequent O-sil- ylation, nucleophilic addition of organometallic reagents proceeded with high regio- and stereo- selectivity at 4-position. Substituents

We have now found, that the optimal conditions for the synthesis of compounds 1a–c from urea, chloroaliphatic aldehydes and alkyl acetoacetates in- clude glacial HOAc/dry HCl

These com- pounds were used to prepare a novelseries of enaminones 5, and their reactions with hydrazonoyl halides 1 and 11 gave triazoloisoquinolines 8 and 13, respectively, with

Here we present an improved and concise strategy for the syn- thesis of oligonucleotides that bear 5-(mercaptomethyl)- 2'-deoxyuridine moieties in principle at any desired posi-

In this short note, we introduce the synthesis of the novel 2'- methylseleno-2'-deoxyribonucleoside triphosphates of adenosine and guanosine (2 '-SeCH r ATP and 2'-SeCH