Search results for "synthesis"
showing 10 items of 2844 documents
Synthesis of Enantiopure 6,11‐Methylene Lipoxin B4Methyl Ester
2021
Analysis of Invariant Chain Processing in 3 Day Cultured Rat Langerhans Cells
1995
MHC class II molecules, critical peptide binding elements involved in the presentation of exogenous antigen to T helper cells, are expressed constitutively by Langerhans cells (LC) within their epidermal microenvironment. Several studies in mouse and man demonstrated, that short term in vitro culture of LC entails remarkable functional and penotypic alterations, including a profound increase of class II elements exposed at the LC’s surface1. Biosynthetic analysis revealed a downregulation of class II synthesis during the culture period2,3. In recent work on rat LC we described the uncoupling of the coordinately regulated biosynthesis of class II and invariant chain proteins in the course of…
Soft hydrothermal synthesis of new microporous materials based on phosphate-like species
1994
ABSTRACTFactors controlling hydrothermal synthetic procedures are not well understood. A good knowledge of the solution chemistry of precursor species is the best reference for the design of rational procedures. Examples of the predictive character of simple models in order to rationalize complex syntheses are discussed in detail.
Book Review: Cycloaddition Reactions in Organic Synthesis. By W. Carruthers
1992
Microwave-Driven Hydrothermal Synthesis of Oxide Nanopowders for Applications in Optoelectronics
2005
Solid-Phase Synthesis of Oligo(p-benzamide) Foldamers
2006
[reaction: see text] A coupling protocol has been developed which allows the synthesis of oligo(p-benzamide)s on solid support. Aromatic carboxylic acids are activated in situ with thionyl chloride and used to acylate secondary aromatic amines. N-p-Methoxy benzyl (PMB) as well as N-hexyl protected monomers were investigated. Heterosequences of both monomers were synthesized. Such nanoscale objects are important building blocks for supramolecular chemistry.
ChemInform Abstract: Aza-Henry Reaction of Isatin Ketimines with Methyl 4-Nitrobutyrate en Route to Spiro[piperidine-3,3′-oxindoles].
2016
A new enantioselective route to spiro[piperidine-3,3′-oxindoles] from isatin ketimines is described. The aza-Henry reaction of N-Boc-isatin ketimines with methyl 4-nitrobutyrate in the presence of a Ph2BOX-CuBr2 complex provided the corresponding nitro amino esters with good diastereoselectivity and excellent enantioselectivity (up to >99% ee). The aza-Henry adducts were transformed into spiro[piperidine-3,3′-oxindoles] after reduction of the nitro group to oxime, and cleavage of the N-Boc group and lactamisation.
ChemInform Abstract: Highly Enantioselective Aza-Henry Reaction with Isatin N-Boc Ketimines.
2014
The asymmetric aza-Henry reaction of isatin N-Boc-ketimines (I) with nitromethane in the presence of a Cu-Ph-box complex leads to a series of N-Boc-protected nitroamines (III) with high enantioselectivity in most cases.
Organocatalytic enantioselective aza-Friedel–Crafts reaction of 2-naphthols with benzoxathiazine 2,2-dioxides
2015
An organocatalytic enantioselective aza-Friedel–Crafts addition of 2-naphthols to benzoxathiazine 2,2-dioxides is described using a quinine-derived bifunctional catalyst. The method allows the use of a wide range of aromatic compounds as nucleophiles, including 1-naphthol and sesamol, and benzoxathiazines 2,2-dioxides, expanding the existing state of the art enantioselective synthesis of aminomethylnaphthol derivatives.
ChemInform Abstract: Organocatalytic Enantioselective Aza-Friedel-Crafts Reaction of 2-Naphthols with Benzoxathiazine 2,2-Dioxides.
2015
An organocatalytic enantioselective aza-Friedel–Crafts addition of 2-naphthols to benzoxathiazine 2,2-dioxides is described using a quinine-derived bifunctional catalyst. The method allows the use of a wide range of aromatic compounds as nucleophiles, including 1-naphthol and sesamol, and benzoxathiazines 2,2-dioxides, expanding the existing state of the art enantioselective synthesis of aminomethylnaphthol derivatives.