Search results for "Reaction sequence"
showing 10 items of 13 documents
Sequential Nucleophilic−Electrophilic Reactions Selectively Produce Isomerically Pure Nona‐ B ‐Substituted o ‐Carborane Derivatives
2003
Nine equal substituents on the intensively studied o-carborane have been obtained for the first time by a combined nucleophilic-electrophilic reaction sequence. Iodine and methyl groups have been introduced to prove the generality of the method. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)
Ein neuer weg zur herstellung von oligomeren aus acryl- und vinylverbindungen; modell einer matrizenreaktion
1966
In einer Reihe vorangehender Untersuchungen wurde die Herstellung molekulareinheitlicher, phenolischer Mehrkernverbindungen beschrieben. Sie besitzen je Phenolbaustein eine phenolische Hydroxylgruppe, wie systematisch untersuchte Acylierungen sowie Methylierung und Arylierung dieser Mehrkernverbindungen zeigen. In der vorliegenden Mitteilung wurde bei einer Zwei- und Dreikernverbindung an den phenolischen Hydroxylgruppen mit Acrylsaurechlorid umgesetzt, so das die entstandenen Verbindungen so viele polymerisationsfahige Reste wie phenolische Bausteine besasen. Die Polymerisation der Acrylsaurederivate in sehr groser Verdunnung gab oligomere Leiterverbindungen, die durch alkalische Hydrolyse…
Synthesis of β- and γ-carbolines via ruthenium and rhodium catalysed [2+2+2] cycloadditions of yne-ynamides with methylcyanoformate
2011
A flexible approach towards substituted β- and γ-carbolines based on transition metal catalysed [2+2+2] cycloaddition reactions between functionalised yne-ynamides and methylcyanoformate is described. The versatility of this new reaction sequence is demonstrated by its application in the total synthesis of the marine natural product eudistomin U.
4,4′‐Distyrylazobenzol als Mesogen
1992
4,4′-Distyrylazobenzene as Mesogen From 3,4-dihydroxybenzaldehyde (1) the tetraalkoxy-substituted 4,4′-distyrylazobenzenes (E,E,E)-5a – c are synthesized. A similar reaction sequence leads from ethyl 3,4,5-trihydroxy-benzoate (6) to the hexaalkoxy-substituted 4,4′-distyrylazobenzenes (E,E,E)-11 b, c. With the exception of 5a all products show thermotropic LC properties. Smectic phases have been characterized by polarizing microscopy and by differential scanning calorimetry.
Synthesis of 4(5)-phenacyl-imidazoles from isoxazole side-chain rearrangements
2010
A novel base-induced rearrangement of isoxazoles into imidazole derivatives is reported. In the isoxazole series, this represents the first example of a three-atom side-chain rearrangement involving a CNC sequence. The reactions are carried out under nitrogen and produced 2-aryl-4(5)-phenacyl-5(4)-phenyl-imidazoles in high yields. In the presence of oxygen, a cascade rearrangement-oxidation reaction sequence was observed and imidazole derivatives bearing an oxidized side-chain were isolated.
The Di-Tert-Butyl Oxymethylphosphonate Route to the Antiviral Drug Tenofovir
2020
<div>The present manuscript describes a simple, two step synthesis of tenofovir from HPA through phosphonomethalation with a novel doubly protected oxymethylphosphonate electrophile. The crystalline electrophile can be prepared in a simple reaction sequence and can be deblocked more easily than its ditehyl analogue involved in the current commercial process for making the drug.</div><div>The approach is general and can also be used for the preparation of related antivirals and the synthesis of adefovir is described as well.<br></div>
A Short Synthesis of Polysubstituted Pyrrolidines via α-(Alkylideneamino)nitriles
2004
α-(Alkylideneamino)nitriles can be deprotonated under mild conditions. Their conjugated anions react with enones in a 1,4-addition to yield δ-keto-α-(alkylideneamino)nitriles which in turn can be reduced to form pyrrolidines in a one-pot reaction sequence.
ChemInform Abstract: A New Strategy for the Synthesis of Fluorinated 3,4-Dihydropyrimidinones.
2010
A new family of 3,4-dihydropyrimidinones (DHPMs) bearing fluorinated substituents at C6 have been prepared from gem-difluorinated nitriles, alkyl 3-butenoates and iso(thio)cyanates. This novel Biginelli-type process relies on the γ-addition of the ester-derived enolate to fluorinated nitriles. A tandem nucleophilic addition aza-Michael reaction sequence completes the synthetic process.
ChemInform Abstract: Reactions of the Hydrofluoroborate Salts of Open-Chain Analogues of Reissert Compounds with Some α,β-Ethylenic Esters.
2010
The reaction of the hydrofluoroborate salt of an open-chain analogue of a Reissert compound with some α,β-ethylenic esters does not give a [4 + 2] cycloadduct, as previously described in the case of ethyl acrylate. The reaction starts with a 1,3-dipolar cycloaddition of a munchnone imine 5c, d. The [3 + 2] cycloadducts 13 evolve via a rearrangement–condensation sequence to give a substituted 2-pyridone derivative 18 or 19. The proposed mechanism has been verified by the isolation and structural X-ray analysis of some compounds of the reaction sequence.
ChemInform Abstract: Studies on the Biosynthesis of Paraherquamide. Construction of the Amino Acid Framework.
2010
Abstract It has been previously established in this laboratory that the β-methyl-β-hydroxyproline moiety of the potent anthelmintic agent paraherquamide A, is biosynthetically derived from l -isoleucine. The downstream events from l -Ile to paraherquamide A have now been investigated. The synthesis of [1- 13 C]-labeled l -β-methylproline is described by means of a Hoffman–Loeffler–Freytag reaction sequence from [1- 13 C]- l -Ile. This amino acid is shown to be a direct biosynthetic precursor to paraherquamide A by feeding and incorporation experiments in growing cultures of Penicillium fellutanum . Three tryptophan-containing dipeptides of l -β-methylproline have been constructed: [ 13 C 2 …