A novel one-pot method for the preparation of pyrazoles by 1,3-dipolar cycloadditions of diazo compounds generated in situ.
about
Synthesis of Novel Pyrazoles via [2+3]-Dipolar Cycloaddition Using Alkyne Surrogates.C-H bonds as ubiquitous functionality: a general approach to complex arylated pyrazoles via sequential regioselective C-arylation and N-alkylation enabled by SEM-group transposition.Pyrazoles as potential anti-angiogenesis agents: a contemporary overview.N-Tosylhydrazones: versatile synthons in the construction of cyclic compounds.Novel pyrazole and indazole derivatives: synthesis and evaluation of their anti-proliferative and anti-angiogenic activities.A facile and convenient synthesis of some novel hydrazones, Schiff's base and pyrazoles incorporating thieno[2,3-b]thiophenesThe Cremeomycin Biosynthetic Gene Cluster Encodes a Pathway for Diazo Formation.Diazo Compounds as Highly Tunable Reactants in 1,3-Dipolar Cycloaddition Reactions with Cycloalkynes().Synthesis of substituted pyrazoles via tandem cross-coupling/electrocyclization of enol triflates and diazoacetates.One-Pot Synthesis of Polypyrazoles by Click ReactionsCopper-promoted cycloaddition of diazocarbonyl compounds and acetylides.Efficient synthesis of protected cyclopropyl beta-aspartylphosphates.Synthesis and biological evaluation of modified purine homo-N-nucleosides containing pyrazole or 2-pyrazoline moiety.Regioselective one-step synthesis of pyrazoles from alkynes and N-tosylhydrazones: [3+2] dipolar cycloaddition/[1,5] sigmatropic rearrangement cascade.New "green" approaches to the synthesis of pyrazole derivatives.Synthesis of spiro-4H-pyrazole-oxindoles and fused 1H-pyrazoles via divergent, thermally induced tandem cyclization/migration of alkyne-tethered diazo compounds.Direct carboxamidation of cyclic 2-diazo-1,3-diketones by Rh2(OAc)4-catalyzed isocyanide insertion-hydrolysis.[3 + 2] cycloaddition and subsequent oxidative dehydrogenation between alkenes and diazo compounds: a simple and direct approach to pyrazoles using TBAI/TBHP.AgNO2-mediated cleavage of the N-N bond of sulfonylhydrazones and oxygen transfer: access to fulleroisoxazolines via radical cyclization with [60]fullerene.Catalyst-free, one-pot, three-component synthesis of 5-amino-1,3-aryl-₁Η-pyrazole-4-carbonitriles in green media.A base-promoted tandem cycloaddition/air oxidation reaction of electron-deficient conjugated enynes and hydrazines: synthesis of highly substituted pyrazoles.Enantioselective Rhodium(I) Donor Carbenoid-Mediated Cascade Triggered by a Base-Free Decomposition of Arylsulfonyl Hydrazones.Transition-metal-free synthesis of N-(1-alkenyl)imidazoles by potassium phosphate-promoted addition reaction of alkynes to imidazoles.Ionic liquid-supported sulfonyl hydrazine: a useful reagent for traceless synthesis of pyrazoles
P2860
Q33622911-FCA1360C-89D9-435A-860C-644D9463F362Q34198198-9FE955C8-CBDC-4ADA-BA1E-A869CD3F0328Q38253652-62FA1EF8-4402-4F70-ABFA-F09D7BB3C4C6Q39204043-6906DDFA-2CE0-4055-852E-72F3F5F3AB3CQ39329621-E2D541AC-EDCD-4082-9AC3-B1D14F5D1B9CQ39675429-8028533D-2661-418B-B301-23304B791D1DQ41272629-F8C014A3-B54A-4993-9C52-C7AB3269AB04Q41885258-B738FED7-EBC9-4D34-AFC0-B69E00032E05Q41971022-E66E5D4D-4380-407C-A1E8-F0407D4B0777Q42111142-1EF9B240-49F1-4D00-B47D-A20D26042253Q42584705-DB58496D-0B3F-4473-BB80-EB72F4F8AE36Q44760680-FFC686F5-E577-4FAB-BD18-6795D611A083Q45843786-8CC70E62-E08F-47C4-8BB1-0FC7F65D3B6AQ46695317-19FF18C5-5327-44C9-AE6C-85F129D1F2C0Q46971770-0CB786F0-97DC-4AB4-AD01-31B89D9B001FQ47251075-268B1429-AA75-4417-895A-9BC01C09B100Q48686180-77FC03FC-8A34-45C2-9038-12E30EDB05B5Q50221366-3BF8CA01-90A4-462B-927E-9105CC8BAF47Q50260751-018F6D0C-17DA-4962-98EA-BAC762915731Q50481301-6ED27413-BCE1-4BD4-A994-721870E8E405Q50491164-07CE05E8-76C9-48FA-89D6-CDC35FFD2C0EQ50854528-9381D4A4-3227-4F78-99E0-2DFCED6D3F05Q54709602-8E1E10F9-E103-4D21-A66E-624D02D2A920Q58200714-0D973405-3B6E-4BFB-BD14-AB0CD93C47EB
P2860
A novel one-pot method for the preparation of pyrazoles by 1,3-dipolar cycloadditions of diazo compounds generated in situ.
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年学术文章
@wuu
2003年学术文章
@zh-cn
2003年学术文章
@zh-hans
2003年学术文章
@zh-my
2003年学术文章
@zh-sg
2003年學術文章
@yue
2003年學術文章
@zh
2003年學術文章
@zh-hant
name
A novel one-pot method for the ...... o compounds generated in situ.
@en
A novel one-pot method for the ...... o compounds generated in situ.
@nl
type
label
A novel one-pot method for the ...... o compounds generated in situ.
@en
A novel one-pot method for the ...... o compounds generated in situ.
@nl
prefLabel
A novel one-pot method for the ...... o compounds generated in situ.
@en
A novel one-pot method for the ...... o compounds generated in situ.
@nl
P356
P1476
A novel one-pot method for the ...... o compounds generated in situ.
@en
P2093
Javier de Vicente
Roger V Bonnert
P304
P356
10.1021/JO0268409
P407
P577
2003-06-01T00:00:00Z