Simple conversion of enamines to 2H-azirines and their rearrangements under thermal conditions.
about
3,5-dimethylisoxazoles act as acetyl-lysine-mimetic bromodomain ligands.Synthesis of highly functionalized 2,2'-bipyridines by cyclocondensation of β-ketoenamides - scope and limitations.Recent advances in indole syntheses: new routes for a classic target.Identification of specific markers for amphetamine synthesised from the pre-precursor APAAN following the Leuckart route and retrospective search for APAAN markers in profiling databases from Germany and the Netherlands.Hypervalent iodine(III)-induced methylene acetoxylation of 3-oxo-N-substituted butanamides.Fe(II)-catalyzed amination of aromatic C-H bonds via ring opening of 2H-azirines: synthesis of 2,3-disubstituted indolesInvestigation on the reactivity of α-azidochalcones with carboxylic acids: Formation of α-amido-1,3-diketones and highly substituted 2-(trifluoromethyl)oxazoles.Cu(II)-catalyzed domino reaction of 2H-azirines with diazotetramic and diazotetronic acids. Synthesis of 2-substituted 2H-1,2,3-triazoles.α-Diazo oxime ethers for N-heterocycle synthesis.Hypervalent iodine(III)-induced oxidative [4+2] annulation of o-phenylenediamines and electron-deficient alkynes: direct synthesis of quinoxalines from alkyne substrates under metal-free conditions.Metal-Free Intermolecular Aminoarylation of Alkynes.Indole Synthesis through Sequential Electrophilic N-H and C-H Bond Activation Using Iodine(III) Reactivity.The organocatalytic asymmetric Neber reaction for the enantioselective synthesis of spirooxindole 2H-azirines.Synthesis of 2H-Azirines by Iridium-Catalyzed Decarboxylative Ring Contraction of Isoxazol-5(4H)-ones.A Neber approach for the synthesis of spiro-fused 2H-azirine-pyrazolone.Divergent reactivity of α-oximino carbenoids: facile access to 2-isoxazolines and 2H-azirines.Synthesis of trifluoromethylated 2H-azirines through Togni reagent-mediated trifluoromethylation followed by PhIO-mediated azirination.Efficient Synthesis of Indole Derivatives via Tandem Cyclization Catalyzed by Magnetically Recoverable Palladium/Magnetite (Pd-Fe3 O4 ) Nanocrystals
P2860
Q35280915-EBE36892-4384-410F-9491-008D87C0AC95Q36112471-1B28DADA-57DD-45C0-B9D0-B3A02377ED71Q37903720-CA7393DD-99B9-4EF8-8C35-1F3EDBF2E7C0Q38600497-4495A7DA-CA07-4371-BD9E-700532F03E89Q38898727-8B3A36CE-EDB6-4231-AEB9-F5361BDDCB38Q41777189-89BA3B97-F775-4509-BDC6-D974C8B0E786Q43153971-73DE35E6-6FF8-4F27-97E1-75E3149EB4E0Q44602989-CA527BFE-EA9B-41FF-AB85-8F26BEEAA910Q46364279-502BC55A-D308-41E0-9DA9-54525185AA4FQ46701402-AAFE235D-9732-453D-A698-4403B74347D3Q48127189-5217CFDA-82A8-49F9-AE77-22020E25B7AFQ48276975-F166D7B8-852A-413A-A3B3-8AE58CD33F50Q51106121-5AD51FA5-91F4-409E-9ECD-80B52BF329D6Q51352849-E7771312-CC8B-4FD5-823D-340448854768Q51556536-9C7C73C3-85E8-40FC-B650-D03AEA1E2A99Q51561082-D7A9544E-14E9-4605-A268-7156BDB40F71Q55440554-2BD9B026-8FEC-4C95-B47C-0D7692BA183CQ57557935-1CD04FCC-8F4B-4A06-B2ED-D33723A2DD9D
P2860
Simple conversion of enamines to 2H-azirines and their rearrangements under thermal conditions.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
2009年论文
@zh
2009年论文
@zh-cn
name
Simple conversion of enamines ...... ents under thermal conditions.
@en
Simple conversion of enamines ...... ents under thermal conditions.
@nl
type
label
Simple conversion of enamines ...... ents under thermal conditions.
@en
Simple conversion of enamines ...... ents under thermal conditions.
@nl
prefLabel
Simple conversion of enamines ...... ents under thermal conditions.
@en
Simple conversion of enamines ...... ents under thermal conditions.
@nl
P2093
P356
P1433
P1476
Simple conversion of enamines ...... ents under thermal conditions.
@en
P2093
P304
P356
10.1021/OL9006663
P407
P577
2009-06-01T00:00:00Z