Results 171 to 180 of about 8,110 (222)

Synthesis of Novel Sugar Amino Acids by Curtius Rearrangement

open access: closedEuropean Journal of Organic Chemistry, 2003
AbstractSugar amino acids (SAAs) bearing an amine group on the anomeric position are a challenging class of SAAs to synthesize due to the inherent instability of glycosylamines. We developed a novel synthetic strategy towards both furanoid and pyranoid δ‐SAAs of this type, based on a Curtius rearrangement. The latter reaction, which is known to proceed
Renate M. van Well   +7 more
openalex   +3 more sources

Curtius-rearrangement of “rigid” azides

open access: closedTetrahedron Letters, 1964
Walter Lwowski   +3 more
openalex   +3 more sources

Some Applications of the Curtius Rearrangement

Journal of the Chemical Society, Perkin Transactions 1, 1983
Pairs of optically pure enantiomers of substituted 1,1 -diamines have been prepared from the azides of L-amino-acids via the Curtius rearrangement.This synthesis is based on the interchange of two groups attached to the asymmetrically substituted tetrahedral α-carbon atom of the parent amino acid.
Iphigenia Photaki   +1 more
openaire   +2 more sources

Synthesis of 2,2‐[60]Fullerenoalkylamines (IV) via the Curtius Rearrangement. [PDF]

open access: possibleChemInform, 2007
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Kazuhiko Saigo   +2 more
openaire   +2 more sources

ChemInform Abstract: Synthesis of 2‐Arylethylamines by the Curtius Rearrangement. [PDF]

open access: possibleChemInform, 2010
AbstractNovel chemical syntheses of amphetamines (V), (VIII) and (XV) as well as wescaline (XI) using the Curtius rearrangement as key reaction are developed.
openaire   +2 more sources

Improved Preparation of Tyramine by Curtius Rearrangement

Chinese Journal of Chemistry, 2009
AbstractAn improved and facile preparation of tyramine [2‐(p‐hydroxyphenyl)ethylamine] was described, which starts from phenol and acrylonitrile to form β‐(p‐hydroxyphenyl) propionic acid via Friedel‐Craft's alkylation and nitrile hydrolysis. After hydrazinolysis and a subsequent Curtius rearrangement, tyramine was obtained in 30.2% total yield.
Li-Xin Wang   +5 more
openaire   +3 more sources

Curtius-type rearrangement of a sulphonyl azide

Journal of the Chemical Society D: Chemical Communications, 1969
Six products have been identified from the thermolysis of mesitylene-2-sulphonyl azide in dodecane: two are derived from a Curtius-type rearrangement of the corresponding sulphonyl nitrene.
Rudolph A. Abramovitch, W. D. Holcomb
openaire   +2 more sources

ChemInform Abstract: Synthesis of (‐)‐Oseltamivir by Using a Microreactor in the Curtius Rearrangement.

ChemInform, 2011
AbstractThe method avoids the isolation of the potentially hazardous azide intermediate and can be scaled up as an industrial process.
Bojan P. Bondzic   +3 more
openaire   +3 more sources

ChemInform Abstract: The Use of Curtius Rearrangement in the Synthesis of 4‐Aminothiazolidines.

ChemInform, 1999
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Edson R. Costenaro   +2 more
openaire   +3 more sources

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