P185
Synthesis of multivalent carbohydrate mimetics with aminopolyol end groups and their evaluation as L-selectin inhibitors.A short formal total synthesis of strychnine with a samarium diiodide induced cascade reaction as the key step.Synthesis of new enantiopure poly(hydroxy)aminooxepanes as building blocks for multivalent carbohydrate mimeticsSynthesis of highly functionalized 2,2'-bipyridines by cyclocondensation of β-ketoenamides - scope and limitations.Amino sugars and their mimetics via 1,2-oxazines.Samarium diiodide induced ketyl-(het)arene cyclisations towards novel N-heterocycles.Alkoxyallenes as building blocks for organic synthesis.A practical two-step procedure for the preparation of enantiopure pyridines: Multicomponent reactions of alkoxyallenes, nitriles and carboxylic acids followed by a cyclocondensation reaction.Novel Alkoxy-Substituted Dipyrrins and Near-IR BODIPY Dyes-Preparation and Photophysical Properties.The novel synthetic ether lipid inositol-C2-PAF inhibits phosphorylation of the tyrosine kinases Src and FAK independent of integrin activation in transformed skin cells.Antitumor effects of guanosine-analog phosphonates identified by molecular modelling.Human polymerase alpha inhibitors for skin tumors. Part 2. Modeling, synthesis and influence on normal and transformed keratinocytes of new thymidine and purine derivatives.Preparation of pyridine-3,4-diols, their crystal packing and their use as precursors for palladium-catalyzed cross-coupling reactionsStrychnine as Target, Samarium Diiodide as Tool: A Personal Story.Evolution of a short route to strychnine by using the samarium-diiodide-induced cascade cyclization as a key step.Highly substituted benzannulated cyclooctanol derivatives by samarium diiodide-induced cyclizations.Carbohydrate-auxiliary assisted preparation of enantiopure 1,2-oxazine derivatives and aminopolyols.Iodination of carbohydrate-derived 1,2-oxazines to enantiopure 5-iodo-3,6-dihydro-2H-1,2-oxazines and subsequent palladium-catalyzed cross-coupling reactionsStereoselective synthesis of tricyclic compounds by intramolecular palladium-catalyzed addition of aryl iodides to carbonyl groups.Addition of lithiated enol ethers to nitrones and subsequent Lewis acid induced cyclizations to enantiopure 3,6-dihydro-2H-pyrans - an approach to carbohydrate mimetics.Palladium-catalyzed cross coupling reactions of 4-bromo-6H-1,2-oxazines.Synthesis of rigid p-terphenyl-linked carbohydrate mimetics.Stereodivergent synthesis of jaspine B and its isomers using a carbohydrate-derived alkoxyallene as C3-building blockInternally protected amino sugar equivalents from enantiopure 1,2-oxazines: synthesis of variably configured carbohydrates with C-branched amino sugar units.A three-component synthesis of beta-alkoxy-beta-keto-enamides--flexible precursors for 4-hydroxypyridine derivatives and their palladium-catalysed reactions.Three-component synthesis of perfluoroalkyl- or perfluoroaryl-substituted 4-hydroxypyridine derivatives and their palladium-catalyzed coupling reactions.Highly diastereoselective samarium diiodide induced cyclizations of new 3-substituted indole derivatives.Enantiopure aminopyrans by a Lewis acid promoted rearrangement of 1,2-oxazines: versatile building blocks for oligosaccharide and sugar amino acid mimetics.A stereoselective and short total synthesis of the polyhydroxylated gamma-amino acid (-)-detoxinine, based on stereoselective preparation of dihydropyrrole derivatives from lithiated alkoxyallenes.A new color of the synthetic chameleon methoxyallene: synthesis of trifluoromethyl-substituted pyridinol derivatives: an unusual reaction mechanism, a remarkable crystal packing, and first palladium-catalyzed coupling reactions.Regioselective samarium diiodide induced couplings of carbonyl compounds with 1,3-diphenylallene and alkoxyallenes: a new route to 4-hydroxy-1-enol ethers.A new ring closure approach to enantiopure 3,6-dihydro-2H-pyrans: stereodivergent access to carbohydrate mimetics.A new and flexible synthesis of 4-hydroxypyridines: rapid access to caerulomycins A, E and functionalized terpyridines.Three-component synthesis of highly functionalized 5-acetyloxazoles.Inhibition of selectin binding by colloidal gold with functionalized shells.Sugars, alkaloids, and heteroaromatics: exploring heterocyclic chemistry with alkoxyallenes.Ruthenium Complexes with Strongly Electron-Donating Terpyridine Ligands: Effect of the Working Electrode on Electrochemical and Spectroelectrochemical Properties.Alkoxyallene-Based Stereodivergent Syntheses of (-)-Hyacinthacine B4 and of Putative Hyacinthacine C5 Epimers: Proposal of Hyacinthacine C5 Structure.Linear and cyclic hybrids of alternating thiophene-amino acid units: synthesis and effects of chirality on conformation and molecular packing.A Flexible Terpyridine Derivative Interacts Specifically with G-Quadruplexes.
P50
Q30977626-ADA5AFCB-A6F8-4427-9CA6-FF5823827A7EQ34138528-2002E794-0E11-4E16-AB05-18AAD39EC521Q35113626-BF9FC354-6830-4D7C-9FAF-2155E0DB8601Q36112471-715186F4-3B54-4BB8-91D1-C1BC4D822091Q37683480-712FE627-3AA8-445C-A22C-29B17FCDFAE2Q37829643-DC0396FD-4211-4D10-930A-40F9E199D758Q38189255-E175EB8C-9769-4DBE-AAAB-7E27EC094406Q38365275-3FAB25CF-D337-4100-9752-A5771F9BAFEBQ38707127-1DBA58EC-BBA6-4B5E-BE5E-E7C930FED079Q39592441-4BC4DC4F-9DCC-41AE-9439-B285E4DA31D1Q39684670-62B9AE97-FE6E-4AA9-98AF-92A381E82E0BQ39728918-998E3D1D-06F4-4B80-966C-545EDEFE25AAQ40681242-7754F03C-0857-471D-A0A4-7DA458ACA12CQ41083187-7523A871-A62A-49D1-85B5-B61B83DA39D5Q41331386-A7051EED-BEB2-4B0F-A6ED-B73948A0913AQ41854598-EBFC3144-3996-4537-95CC-0DF287CA4AD2Q42223882-6857377C-5985-4431-9EE0-1E1803C7A578Q42330249-ED3A8220-5DD9-4EFE-8387-6278E7765B88Q42367132-874AF277-6613-434A-83D2-3C31E0DA279FQ42549622-EF7FB35E-1075-4903-A51E-88018A50A7ABQ42649601-83BF3898-FD9C-480F-88CB-4778DDE79B4BQ42705552-46691BA9-9FAF-4C12-B4DD-9150450BE6C8Q42782382-B736A4DF-1CC4-447F-9AF4-BBB69AE05BAEQ42908137-CAEDD2EE-833A-4BC4-B55C-AE24F2DC1432Q43062112-2B2B1F81-7887-4F6E-AA1A-99635ECEDA66Q43210487-49F0D4C6-040E-4CA2-9E12-A2C1226E91BAQ43261154-9F6AE055-D71F-43F9-84CC-F14AF056DF58Q43271575-4B4FC5E4-1E54-4A92-9D3D-10912BFA6A3CQ44367609-8F04307D-0E5A-47C9-AD97-2218CC89A905Q45047781-BF0B8CD7-647C-4645-B5FD-A0264DC36880Q45062737-1B8F6A65-3176-4FBB-A877-580B73AA8EA8Q45868832-F8EFEDB0-02CC-491E-AB7C-4B9CB135D58AQ45966015-D1577990-9332-412C-873D-7676F9014667Q46039742-517C90B0-A4D6-4A05-B77D-FD11D26E70B5Q46123372-05C4EA68-8039-4080-A336-C58761E96D30Q46315638-B0E85145-21EF-4920-9E77-C42B457D89ACQ48144966-0EAFA9BE-4F88-48F4-8575-21C7AFEAC3D6Q48179576-E924693D-674C-454D-99C5-088136212DA4Q51778487-A5158C61-1103-43F3-B5B4-64A070A94439Q52849932-E0DD9E9A-CFC1-43DE-886B-7EFA1C2D6FD9
P50
description
Duits scheikundige
@nl
German chemist
@en
German chemist
@en-ca
German chemist
@en-gb
Saksamaa keemik
@et
ceimiceoir Gearmánach
@ga
chimist german
@ro
chimiste allemand
@fr
deutscher Chemiker
@de
kimist gjerman
@sq
name
Hans-Ulrich Reissig
@en
Hans-Ulrich Reissig
@es
Hans-Ulrich Reissig
@nl
Hans-Ulrich Reissig
@sl
Hans-Ulrich Reißig
@ca
Hans-Ulrich Reißig
@da
Hans-Ulrich Reißig
@de
Hans-Ulrich Reißig
@fr
Hans-Ulrich Reißig
@nds
Hans-Ulrich Reißig
@pt
type
label
Hans-Ulrich Reissig
@en
Hans-Ulrich Reissig
@es
Hans-Ulrich Reissig
@nl
Hans-Ulrich Reissig
@sl
Hans-Ulrich Reißig
@ca
Hans-Ulrich Reißig
@da
Hans-Ulrich Reißig
@de
Hans-Ulrich Reißig
@fr
Hans-Ulrich Reißig
@nds
Hans-Ulrich Reißig
@pt
prefLabel
Hans-Ulrich Reissig
@en
Hans-Ulrich Reissig
@es
Hans-Ulrich Reissig
@nl
Hans-Ulrich Reissig
@sl
Hans-Ulrich Reißig
@ca
Hans-Ulrich Reißig
@da
Hans-Ulrich Reißig
@de
Hans-Ulrich Reißig
@fr
Hans-Ulrich Reißig
@nds
Hans-Ulrich Reißig
@pt
P108
P269
P1207
n2015168079
P1412
P1559
Hans-Ulrich Reißig
@de
P166
P184
P19
P21
P214
P269
P31
P569
1949-05-09T00:00:00Z