about
Collagen cross linking agents: design and development of a multifunctional cross linker.Conjugated polymer and drug co-encapsulated nanoparticles for chemo- and photo-thermal combination therapy with two-photon regulated fast drug release.Places and chemistry: Strasbourg--a chemical crucible seen through historical personalities.Recent developments in enediyne chemistry.Gas extrusion in natural products total synthesis.Photo-responsive polymeric micelles.Photochemical transformations accelerated in continuous-flow reactors: basic concepts and applications.Photochemistry and photophysics at extended seams of conical intersection.Taming hazardous chemistry in flow: the continuous processing of diazo and diazonium compounds.A flexible and stereoselective synthesis of azetidin-3-ones through gold-catalyzed intermolecular oxidation of alkynes.Fluorinated diazoalkanes - a versatile class of reagents for the synthesis of fluorinated compounds.Recent applications of the 1,2-carbon atom migration strategy in complex natural product total synthesis.Early events in the photochemistry of 5-diazo Meldrum's acid: formation of a product manifold in C-N bound and pre-dissociated intersection seam regions.Masked red-emitting carbopyronine dyes with photosensitive 2-diazo-1-indanone caging group.Two-photon degradable supramolecular assemblies of linear-dendritic copolymers.2-Diazo-1-(4-hydroxyphenyl)ethanone: a versatile photochemical and synthetic reagent.Catalytic asymmetric homologation of α-ketoesters with α-diazoesters: synthesis of succinate derivatives with chiral quaternary centers.Total synthesis and biological evaluation of grassypeptolide A.Ring Expansion, Photoisomerization, and Retrocyclization of 1,4,2-Diazaboroles.Nitrogen enriched mesoporous organic polymer anchored copper(II) material: an efficient and reusable catalyst for the synthesis of esters and amides from aromatic systems.Malonic Acid Diazoesters for C-H Insertion Crosslinking (CHic) Reactions: A Versatile Method for the Generation of Tailor-Made Surfaces.Functionalization of 3-Iridacyclopentenes.A Synthesis of (±)-Aplydactone.QM/MM nonadiabatic dynamics simulations on photoinduced Wolff rearrangements of 1,2,3-thiadiazole.Synthesis with perfect atom economy: generation of diazo ketones by 1,3-dipolar cycloaddition of nitrous oxide at cyclic alkynes under mild conditions.Direct carboxamidation of cyclic 2-diazo-1,3-diketones by Rh2(OAc)4-catalyzed isocyanide insertion-hydrolysis.Ring contraction of metallabenzooxirene to metal carbonyl complexes - a comparative study with the Wolff rearrangement of oxirene and benzooxirene.Catalyst- and halogen-free regioselective Friedel-Crafts α-ketoacylations.Biocompatible micelles based on comb-like PEG derivates: formation, characterization, and photo-responsiveness.Synthesis of aryldiazoacetates through palladium(0)-catalyzed deacylative cross-coupling of aryl iodides with acyldiazoacetates.Photoinduced Ultrafast Wolff Rearrangement: A Non-Adiabatic Dynamics PerspectiveIntegrated Micro-Flow Synthesis Based on Photochemical Wolff Rearrangement
P2860
Q31141823-D22388A8-127A-461B-9D5B-95E1A9EAD07EQ35546710-2DB4A260-9193-4EA5-9F65-B8DB518D86FDQ37859634-099C2CEB-1BF3-49FE-BDD6-D97168CF512FQ37994131-A4AF36F3-A042-4667-A0BB-BBA7140505B1Q38039828-841E132F-07B3-43EF-9023-B9CF525E8EABQ38232193-9A9FDA3F-183A-468E-BAC4-FD101851C064Q38233279-E36C050D-6848-42C6-A81E-EB3EB2646D83Q38243360-C56682F0-C8B4-4457-8A55-971541DB2E36Q38268907-7EEFBB56-F853-4192-AA7D-D56D8EE05EC2Q38322024-D2CE55DA-763A-4F63-85CF-CDAE57AC3E39Q38976911-664FA79A-1B2A-40FB-980E-8EA4B7BBF55CQ39204066-26F0F999-6241-42C4-A1E1-B3AEA60D45F6Q39228173-5CBF0B12-1F0E-4BE4-A919-2B91F27C42E6Q39417599-C837734D-E63F-4982-9996-3D2BBACB245EQ40090841-EF75760F-0865-4121-87CD-E590768CFAF2Q41990439-0E84B68D-9794-4A1A-A124-32EE2BA5386BQ44610025-35762BE5-47A9-4156-86F7-32EBF0991419Q46093378-1E92902A-564D-46D6-BBD5-3CEBC4FB03A6Q47687710-CE06920C-B119-43AB-A927-36F0A46D479FQ47738076-D0601E03-851C-4F53-B3DD-F0E7FA02CF23Q47748280-A24F8883-3346-427D-BDEA-D70906044171Q47890181-8113AE7F-D489-428F-8217-7D29269F2A68Q48181793-CA064844-1A1F-4A6B-A633-FCE68DB3B7EEQ48253193-1CCC7209-F6E9-417A-8FAD-B29B7120996CQ48260228-A7CB1E9A-F52E-4E2D-8D34-E69974AC6FB2Q48686180-2D52E14A-1D86-47D9-BBA0-5F3921CEDB20Q49633830-98537B16-A950-471D-853E-F669EE2E7DA8Q50494644-551A04E1-5878-4B50-A807-F24CE2044605Q52612534-B027CF71-E71E-47BE-BB71-32CED8A8CD49Q53453868-5CAE111A-C50C-4D50-A834-DCC90B158BADQ57397745-23C8DA88-AFE4-41FE-AAEB-7642F1DD7144Q58615050-BA577FE1-A5FE-4B40-BF9A-3446C8A1FA67
P2860
description
2002 nî lūn-bûn
@nan
2002 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
100 Years of the Wolff Rearrangement
@ast
100 Years of the Wolff Rearrangement
@en
type
label
100 Years of the Wolff Rearrangement
@ast
100 Years of the Wolff Rearrangement
@en
prefLabel
100 Years of the Wolff Rearrangement
@ast
100 Years of the Wolff Rearrangement
@en
P3181
P1476
100 Years of the Wolff Rearrangement
@en
P2093
Wolfgang Kirmse
P3181
P356
10.1002/1099-0690(200207)2002:14<2193::AID-EJOC2193>3.0.CO;2-D
P577
2002-07-01T00:00:00Z