Direct catalytic asymmetric addition of allyl cyanide to ketones via soft Lewis acid/hard Brønsted base/hard Lewis base catalysis.
about
Enantioselective iridium-catalyzed vinylogous Reformatsky-aldol reaction from the alcohol oxidation level: linear regioselectivity by way of carbon-bound enolatesLewis base catalyzed enantioselective additions of an N-silyl vinylketene imine.Enantioselective CuH-Catalyzed Hydroallylation of Vinylarenes.Diastereoselective and enantioselective conjugate addition reactions utilizing α,β-unsaturated amides and lactams.Cyanoalkylation: Alkylnitriles in Catalytic C-C Bond-Forming Reactions.Transition metal catalysis-a unique road map in the stereoselective synthesis of 1,3-polyols.Silyl ketene imines: highly versatile nucleophiles for catalytic, asymmetric synthesis.Direct asymmetric vinylogous aldol reaction of allyl ketones with isatins: divergent synthesis of 3-hydroxy-2-oxindole derivatives.Direct catalytic asymmetric addition of acetonitrile to N-thiophosphinoylimines.Catalytic enantioselective decarboxylative cyanoalkylation of imines by using palladium pincer complexes with C2-symmetric chiral bis(imidazoline)s.A One-Pot Tandem Strategy in Catalytic Asymmetric Vinylogous Aldol Reaction of Homoallylic Alcohols.Catalytic Enantioselective γ-Selective Additions of 2-Allylazaarenes to Activated Ketones.Direct catalytic enantioselective Mannich-type reaction of dichloroacetonitrile using bis(imidazoline)-Pd catalysts.A robust nickel catalyst for cyanomethylation of aldehydes: activation of acetonitrile under base-free conditions.Copper-catalyzed cyclization/aza-Claisen rearrangement cascade initiated by ketenimine formation: an efficient stereocontrolled synthesis of α-allyl cyclic amidines.Cooperative activation of alkyne and thioamide functionalities; direct catalytic asymmetric conjugate addition of terminal alkynes to α,β-unsaturated thioamides.Enantioselective direct vinylogous aldol-cyclization cascade reaction between β,γ-unsaturated amides and o-quinones.
P2860
Q34168946-6C400958-8435-4EA6-BF32-B0C29D95D985Q36486752-38104EAF-79A1-4A63-914F-FFA85F7FB2E5Q36852041-D05DB302-7531-4F0D-97B4-77EB50712CFDQ38482449-572D3A44-1055-4D73-AE71-CE51B5ED723EQ38589856-883BB87D-2A7F-4D72-B3A6-46A8BD75372FQ39038143-B93F2610-B6A4-4BDD-BCCD-31722AFD4701Q42209687-F4F6C3EF-7280-4512-8597-37B14DB6DC0CQ43447754-EB44AD8A-FBF4-4D2B-8CC2-DA5609880B80Q43705763-3893A0A6-1EF1-4C4E-A6BF-54E7CF410899Q45423732-BA36BEC2-18A0-4AA7-AA35-26C6350E11BEQ50791208-51768DD0-0875-4030-BB67-C010419AC00AQ50988511-FFE76C64-7A90-4E56-8713-C42BE5909B97Q51110487-1003841F-3E39-4240-A80B-EDB971678701Q52756994-E41C385B-96EE-4C7D-9782-19FEE23EFDA7Q53511008-FDD21135-1CBD-48FD-9B43-FAD3A1E8D2E6Q54460347-A87AF110-1083-4088-B783-7FC565390231Q54698189-2D5F70D4-BCF2-4205-AF52-0E4C1C2EEE87
P2860
Direct catalytic asymmetric addition of allyl cyanide to ketones via soft Lewis acid/hard Brønsted base/hard Lewis base catalysis.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
@yue
2010年學術文章
@zh-hant
name
Direct catalytic asymmetric ad ...... ase/hard Lewis base catalysis.
@en
Direct catalytic asymmetric ad ...... ase/hard Lewis base catalysis.
@nl
type
label
Direct catalytic asymmetric ad ...... ase/hard Lewis base catalysis.
@en
Direct catalytic asymmetric ad ...... ase/hard Lewis base catalysis.
@nl
prefLabel
Direct catalytic asymmetric ad ...... ase/hard Lewis base catalysis.
@en
Direct catalytic asymmetric ad ...... ase/hard Lewis base catalysis.
@nl
P2093
P356
P1476
Direct catalytic asymmetric ad ...... ase/hard Lewis base catalysis.
@en
P2093
Masakatsu Shibasaki
Naoya Kumagai
Ryo Yazaki
P304
P356
10.1021/JA101687P
P407
P577
2010-04-01T00:00:00Z