About: Highly Enantioselective Catalytic [6+3] Cycloadditions of Azomethine Ylides

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scientific article published on 14 August 2012

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique publié en 2012 (fr) наукова стаття, опублікована в серпні 2012 (uk) im August 2012 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 14 August 2012 (en) artículu científicu espublizáu n'agostu de 2012 (ast)
publication date	wds:Q57006741-E2E3DDF8-E020-472B-A4E8-86A6529DD026
publication date	2012-08-14 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q57006741-55FDB32E-681A-4B47-980D-19F82D60DA1A
language of work or name	English
cites work	wds:Q57006741-1BFF8428-B458-4841-9823-F10048731933 wds:Q57006741-2038A6C8-438B-459E-94BD-6C02407A4A61 wds:Q57006741-2FBAFA6F-3908-4EA0-9800-C419165B3540 wds:Q57006741-368E9B5B-B041-42C2-84B1-0F1C2CA97331 wds:Q57006741-3FC345F9-30B6-47A4-AB14-3428CC123BD8 wds:Q57006741-4310A3B3-E348-4D7B-95D2-93661F98AF3C wds:Q57006741-44CB8410-1982-4736-A895-712FE7B32629 wds:Q57006741-4646C23D-938C-4448-A16D-AC699FD5FEAC wds:Q57006741-4BB4BDE2-116A-4EB3-992C-529121F3E6ED wds:Q57006741-4D105E51-5484-4711-B236-D8CF182054C5 wds:Q57006741-4D826A5B-4E88-4945-9695-B70635FD5286 wds:Q57006741-4DC7D471-ABB5-4E5F-B12D-622FCC86849F wds:Q57006741-56E26F4C-0596-46C2-88F7-087FF85BB0B8 wds:Q57006741-6139352D-C82D-498D-831D-5FFC3DDDDC96 wds:Q57006741-6B21BE56-9935-4120-B8E5-CBA5282A4124 wds:Q57006741-6DBD0AEC-F8FD-45CE-97AF-4FA23C92F27C wds:Q57006741-7C221071-628D-4289-95B4-3C10DF19C0B5 wds:Q57006741-8E442745-F868-4BE7-973C-284F349E7924 wds:Q57006741-8E653975-8C8D-4D43-B110-74698D113B0A wds:Q57006741-977D3B6F-2752-4F86-BC53-57881581E65E wds:Q57006741-98AF10EA-B145-4744-95EB-65C73D3627EC wds:Q57006741-A4268C01-EB77-4BD0-9B75-896270B757D1 wds:Q57006741-A5761256-17ED-4A0C-A006-97E98764FF90 wds:Q57006741-BAFA110A-41B2-48C1-A8D1-7B9E86741B6E wds:Q57006741-D0C74B23-BCA2-45E6-951B-C3CD947E889F wds:Q57006741-D73B74A2-1418-4D25-86E7-71C46424F91D wds:Q57006741-E8536A48-1ED7-4561-AE0B-0C998E8F3785 wds:Q57006741-F3EEC1CA-FB83-433C-A488-363D85F5143C wds:Q57006741-FECFE32F-614E-47B6-988C-A57F76D748FA
cites work	Exploiting [2+2] cycloaddition chemistry: achievements with allenes Catalytic enantioselective 1,3-dipolar cycloaddition reaction of azomethine ylides and alkenes: the direct strategy to prepare enantioenriched highly substituted proline derivatives Intramolecular dipolar cycloaddition reactions of azomethine ylides. Bioactivity-guided navigation of chemical space Biology-inspired synthesis of compound libraries Biology-oriented synthesis Synthesis of natural product inspired compound collections Highly enantioselective synthesis and cellular evaluation of spirooxindoles inspired by natural products Asymmetric organocatalytic cyclization and cycloaddition reactions The dehydro-Diels-Alder reaction. Asymmetric organocatalysis of 4 + 3 cycloaddition reactions Pyrrole, pyrrolidine, pyridine, piperidine and tropane alkaloids Novel dipolarophiles and dipoles in the metal-catalyzed enantioselective 1,3-dipolar cycloaddition of azomethine ylides Enantioselective copper-catalyzed 1,3-dipolar cycloadditions Programmable enantioselective one-pot synthesis of molecules with eight stereocenters Asymmetric synthesis of bicyclo[4.3.1]decadienes and bicyclo[3.3.2]decadienes via [6 + 3] trimethylenemethane cycloaddition with tropones Asymmetric Cu(II) catalyses for cycloaddition reactions based on π-cation or n-cation interactions Recent advances in [2+2+2] cycloaddition reactions Intramolecular 1,3-dipolar cycloaddition reactions in targeted syntheses Enantioselective synthesis of the spirotryprostatin A scaffold Asymmetric Synthesis of Highly Substituted Pyrrolidines by 1,3-Dipolar Cycloadditions of Azomethine Ylides withN-Acryloylproline Benzyl Ester Highly endo-selective and enantioselective 1,3-dipolar cycloaddition of azomethine ylide with alpha-enones catalyzed by a silver(I)/ThioClickFerrophos complex Chiral bis(imidazolidine)pyridine-Cu(OTf)2: catalytic asymmetric endo-selective [3 + 2] cycloaddition of imino esters with nitroalkenes. Transition-metal-catalyzed cycloadditions for the synthesis of eight-membered carbocycles Stereoselective transition metal-catalysed higher-order carbocyclisation reactions exo-Selective asymmetric 1,3-dipolar cycloaddition of azomethine ylides with alkylidene malonates catalyzed by AgOAc/TF-BiphamPhos Multi-component cycloaddition approaches in the catalytic asymmetric synthesis of alkaloid targets New chiral ferrocenyl P,S-ligands for highly diastereo-/enantioselective catalytic [3 + 2] cycloaddition of azomethine ylides with cyclic and acyclic enones Asymmetric Control of 1,3-Dipolar Cycloaddition Reactions with Azomethine Ylides by Means of Proline Esters as Chiral Auxiliary Groups
author name string	wds:Q57006741-5EE213BB-BA6C-4823-8F97-4E48E327C1A2
author name string	Marco Potowski
rdfs:label	Highly Enantioselective Catalytic [6+3] Cycloadditions of Azomethine Ylides (en) Highly Enantioselective Catalytic [6+3] Cycloadditions of Azomethine Ylides (nl)
skos:prefLabel	Highly Enantioselective Catalytic [6+3] Cycloadditions of Azomethine Ylides (en) Highly Enantioselective Catalytic [6+3] Cycloadditions of Azomethine Ylides (nl)
name	Highly Enantioselective Catalytic [6+3] Cycloadditions of Azomethine Ylides (en) Highly Enantioselective Catalytic [6+3] Cycloadditions of Azomethine Ylides (nl)
author	wds:Q57006741-20250F1B-320E-48E4-B50A-6E502114A582 wds:Q57006741-690D59D0-1451-42CB-B0B4-48F9440487F8 wds:Q57006741-992785BF-1F7A-4EAE-A221-C4817730F125 wds:Q57006741-F79DFC0C-A383-43B8-A92F-BA5947FF738C
author	Carsten Strohmann Herbert Waldmann Andrey P. Antonchick Jonathan O Bauer
title	wds:Q57006741-C9487375-BEF4-46F9-9033-6E3641F1A736
title	Highly enantioselective catalytic [6+3] cycloadditions of azomethine ylides (en)
page(s)	wds:Q57006741-81C5C6A2-D09C-4318-8153-903A8414D8F4
page(s)	9512-9516
instance of	wds:Q57006741-204EFF38-943B-4837-A183-576CEBB53357
instance of	scholarly article
main subject	wds:Q57006741-0F3C807A-3C71-4638-9C30-B594751129D7 wds:Q57006741-656BB645-AB0F-456F-83E4-2BD6025C5DEF wds:Q57006741-8FF1F555-C245-4B5F-A9EC-37DCDE8C0AAB wds:Q57006741-FBE72116-5C5B-4096-91B8-60ABB3D8D512
main subject	cycloaddition general chemistry catalysis enantioselectivity
PubMed ID	wds:Q57006741-5032EDA4-80FD-4200-8CF3-73099474DFB0

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