about
Streamlined catalytic asymmetric synthesis of atorvastatin.A one-pot coupling-addition-cyclocondensation sequence (CACS) to 2-substituted 3-acylpyrroles initiated by a copper-free alkynylation.A Direct Synthesis of Highly Substituted π-Rich Aromatic Heterocycles from Oxetanes.Selective ruthenium-catalyzed three-component synthesis of pyrroles."Batch" kinetics in flow: online IR analysis and continuous control.Further evaluation of a series of anti-inflammatory N-pyrrolylcarboxylic acids: effects on the nociception in rats.Zn(OTf)2 promoted rearrangement of 1,2-cyclopropanated sugars with amines: a convenient method for the synthesis of 3-polyhydroxyalkyl-substituted pyrrole derivatives.α-Unsubstituted Pyrroles by NHC-Catalyzed Three-Component Coupling: Direct Synthesis of a Versatile Atorvastatin Derivative.Direct Synthesis of Pyrroles by Dehydrogenative Coupling of Diols and Amines Catalyzed by Cobalt Pincer Complexes.Stabilized pyrrolyl iodonium salts and metal-free oxidative cross-coupling.A metal-free cascade reaction of β-halo-α,β-unsaturated aldehydes and 1,4-dithiane-2,5-diols: synthesis of polycyclic 2-formylthiophenes.Cobalt-catalyzed acceptorless dehydrogenative coupling of aminoalcohols with alcohols: direct access to pyrrole, pyridine and pyrazine derivatives.Palladium(II)-catalysed regioselective synthesis of 3,4-disubstituted quinolines and 2,3,5-trisubstituted pyrroles from alkenes via anti-Markovnikov selectivity.Direct synthesis of pyrroles via a silver-promoted three-component reaction involving unusual imidazole ring opening.Copper-catalyzed C(sp(3))-H functionalization of ketones with vinyl azides: synthesis of substituted-1H-pyrroles.Synthesis of polysubstituted pyrroles via [3 + 2]-annulation of aziridines and β-nitroalkenes under aerobic conditions.The Vinyl Moiety as a Handle for Regiocontrol in the Preparation of Unsymmetrical 2,3-Aliphatic-Substituted Indoles and Pyrroles
P2860
Q43485285-81369AFE-848B-4E18-96DA-CAACF3DC2B4BQ45127938-48E08798-608D-4393-91A1-D011E7A4981FQ45949082-FA09B243-3B17-4A84-831D-F744BD8AB371Q46044648-3D93FAE5-D0D6-4C38-8DEC-74F6B3555BC7Q46061513-0C689BE3-6556-4C07-9467-F0209A130A51Q46971654-84A910E8-3968-4569-82B3-431078AF35E7Q47653461-E15E6C7F-F819-4BAE-8730-604D253E2A52Q48193031-C1000FE0-921C-4BDB-AF70-6701E2F9D6AFQ48248508-9F28B536-F3FD-41EE-B4CF-ABA0A7A41E55Q48310613-04C677E0-21C2-4ACA-BDE4-37B9FF31BE65Q48714006-2BFDA3BB-451C-4D6E-872F-E392C4B1D206Q50052094-D10C0654-5DC2-40B5-BBD6-A7C8F5B0E4B9Q50949707-F33FE5CE-B94E-45EF-974C-3A799687D6BDQ51506306-F506453F-E6F3-49D9-8E45-82A3CC2D7667Q51720458-4503C23A-A764-46CE-BFC9-C3D04F33AEADQ53072408-9708BAA2-63C7-4C88-8B53-334314E25877Q57864730-69805A4E-6670-4D86-998D-E956A47F7FBB
P2860
description
1885 nî lūn-bûn
@nan
1885年の論文
@ja
1885年学术文章
@wuu
1885年学术文章
@zh
1885年学术文章
@zh-cn
1885年学术文章
@zh-hans
1885年学术文章
@zh-my
1885年学术文章
@zh-sg
1885年學術文章
@yue
1885年學術文章
@zh-hant
name
Synthese von Thiophen- und Pyrrolderivaten
@en
Synthese von Thiophen- und Pyrrolderivaten
@nl
type
label
Synthese von Thiophen- und Pyrrolderivaten
@en
Synthese von Thiophen- und Pyrrolderivaten
@nl
prefLabel
Synthese von Thiophen- und Pyrrolderivaten
@en
Synthese von Thiophen- und Pyrrolderivaten
@nl
P356
P1476
Synthese von Thiophen- und Pyrrolderivaten
@en
P2093
P304
P356
10.1002/CBER.18850180175
P577
1885-01-01T00:00:00Z