Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Jensen, Kim Lebek"'
Publikováno v:
Jiang, H, Albrecht, L, Dickmeiss, G, Jensen, K L & Jørgensen, K A 2013, Silyl-Protected Diarylprolinol Catalysts in Organocatalysis . in P I Dalko (ed.), Comprehensive Enantioselective Organocatalysis . Wiley-VCH, pp. 42 .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pure_au_____::0ec0b506b90540e44a2f45c2dcdea4b6
https://pure.au.dk/portal/da/publications/silylprotected-diarylprolinol-catalysts-in-organocatalysis(f634b370-fb2d-4508-b533-47a7eb652a65).html
https://pure.au.dk/portal/da/publications/silylprotected-diarylprolinol-catalysts-in-organocatalysis(f634b370-fb2d-4508-b533-47a7eb652a65).html
Autor:
Jensen, Kim Lebek, Franke, Patrick Tobias, Nielsen, Lasse Tholstrup, Daasbjerg, Kim, Jørgensen, Karl Anker
Publikováno v:
Jensen, K L, Franke, P T, Nielsen, L T, Daasbjerg, K & Jørgensen, K A 2010, ' Anodic Oxidation and Organocatalysis: Direct Regio-and Stereoselective Access to meta-Substituted Anilines by α-Arylation of Aldehydes ', Angewandte Chemie International Edition, vol. 49, pp. 129 .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pure_au_____::5a459468c105424c79bb540824e1795b
https://pure.au.dk/portal/da/publications/anodic-oxidation-and-organocatalysis-direct-regio-and-stereoselective-access-to-metasubstituted-anilines-by-arylation-of-aldehydes(60d63b10-5cdb-11df-8bd0-000ea68e967b).html
https://pure.au.dk/portal/da/publications/anodic-oxidation-and-organocatalysis-direct-regio-and-stereoselective-access-to-metasubstituted-anilines-by-arylation-of-aldehydes(60d63b10-5cdb-11df-8bd0-000ea68e967b).html
Autor:
Jensen, Kim Lebek, Franke, Patrick Tobias, Nielsen, Lasse Tholstrup, Daasbjerg, Kim, Jørgensen, Karl Anker
Publikováno v:
Jensen, K L, Franke, P T, Nielsen, L T, Daasbjerg, K & Jørgensen, K A 2010, ' Combining Anodic Oxidation and Organocatalysis: Direct Regio-and Stereoselective Access to meta-Substituted Anilines by alpha-Arylation of Aldehydes ', Angewandte Chemie International Edition, vol. 49, pp. 129 .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pure_au_____::1becb2ae8566f869fe62070a796c1e00
https://pure.au.dk/portal/da/publications/combining-anodic-oxidation-and-organocatalysis-direct-regio-and-stereoselective-access-to-metasubstituted-anilines-by-alphaarylation-of-aldehydes(08fcc8ca-1b84-40c2-aff3-e416559b27e0).html
https://pure.au.dk/portal/da/publications/combining-anodic-oxidation-and-organocatalysis-direct-regio-and-stereoselective-access-to-metasubstituted-anilines-by-alphaarylation-of-aldehydes(08fcc8ca-1b84-40c2-aff3-e416559b27e0).html
Autor:
Jensen, Kim Lebek, Franke, Patrick Tobias, Arróniz, Carlos, Kobbelgaard, Sara, Jørgensen, Karl Anker
Publikováno v:
Jensen, K L, Franke, P T, Arróniz, C, Kobbelgaard, S & Jørgensen, K A 2010, ' Enantioselective Synthesis of Cyclopentene Carbaldehydes via a Direct Multicatalytic CascadeSequence-Carbocyclization of Aldehydes with Alkynes ', Chemistry: A European Journal, vol. 16, pp. 1750 .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pure_au_____::f4334cb4e41b0aca19d1b5d0c45855a5
https://pure.au.dk/portal/da/publications/enantioselective-synthesis-of-cyclopentene-carbaldehydes-via-a-direct-multicatalytic-cascadesequence--carbocyclization-of-aldehydes-with-alkynes(31c2ebf0-5cdd-11df-8bd0-000ea68e967b).html
https://pure.au.dk/portal/da/publications/enantioselective-synthesis-of-cyclopentene-carbaldehydes-via-a-direct-multicatalytic-cascadesequence--carbocyclization-of-aldehydes-with-alkynes(31c2ebf0-5cdd-11df-8bd0-000ea68e967b).html
Autor:
Monge, David, Franke, Patrick Tobias, Jensen, Kim Lebek, Lykke, Lennart, Jørgensen, Karl Anker
Publikováno v:
Monge, D, Franke, P T, Jensen, K L, Lykke, L & Jørgensen, K A 2010, ' Combining Asymmetric Organo-and Gold-catalysis for the Enantioselective Synthesis of Dihydropyrrol Derivatives ', Chemistry: A European Journal, vol. 16, pp. 9478 .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pure_au_____::251e9190a63013b54df1d2c02b8f125d
https://pure.au.dk/portal/da/publications/combining-asymmetric-organo-and-goldcatalysis-for-the-enantioselective-synthesis-of-dihydropyrrol-derivatives(56f35f2e-4306-42ff-994e-8112153a13f1).html
https://pure.au.dk/portal/da/publications/combining-asymmetric-organo-and-goldcatalysis-for-the-enantioselective-synthesis-of-dihydropyrrol-derivatives(56f35f2e-4306-42ff-994e-8112153a13f1).html
Autor:
Jiang, Hao, Elsner, Petteri, Jensen, Kim Lebek, Falcicchio, Aurelia, Marcos, Vanesa, Jørgensen, Karl Anker
Publikováno v:
Jiang, H, Elsner, P, Jensen, K L, Falcicchio, A, Falcicchio, A, Marcos, V & Jørgensen, K A 2009, ' Achieving Molecular Complexity by Organocatalytic One-Pot Strategies-A Fast Entry for De Novo Synthesis of Sphingoids, Amino Sugars and Polyhydroxylated α-Amino Acids ', Angewandte Chemie International Edition, vol. 48, pp. 6844 .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pure_au_____::fa324278e32740a8d2cd7eb0e0e68f4a
https://pure.au.dk/portal/da/publications/achieving-molecular-complexity-by-organocatalytic-onepot-strategies--a-fast-entry-for-de-novo-synthesis-of-sphingoids-amino-sugars-and-polyhydroxylated-amino-acids(6b2254f0-149c-11df-b95d-000ea68e967b).html
https://pure.au.dk/portal/da/publications/achieving-molecular-complexity-by-organocatalytic-onepot-strategies--a-fast-entry-for-de-novo-synthesis-of-sphingoids-amino-sugars-and-polyhydroxylated-amino-acids(6b2254f0-149c-11df-b95d-000ea68e967b).html
Autor:
Gøgsig, Thomas, Søbjerg, Lina Sveidal, Lindhardt, Anders Thyboe, Jensen, Kim Lebek, Skrydstrup, Troels
Publikováno v:
Gøgsig, T, Søbjerg, L S, Lindhardt, A T, Jensen, K L & Skrydstrup, T 2008, ' Direct Vinylation and Difluorovinylation of Arylboronic Acids Using Vinyl-and 2,2-Difluorovinyl Tosylates via the Suzuki−Miyaura Cross Coupling. ', Journal of Organic Chemistry, vol. 73, no. 9, pp. 3404-3410 .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pure_au_____::61b5d77c00c6b48b79ff876041b80f56
https://pure.au.dk/portal/da/publications/direct-vinylation-and-difluorovinylation-of-arylboronic-acids-using-vinyl-and-22difluorovinyl-tosylates-via-the-suzukimiyaura-cross-coupling(99cf710d-2abc-41e2-aab8-b312a38c72d4).html
https://pure.au.dk/portal/da/publications/direct-vinylation-and-difluorovinylation-of-arylboronic-acids-using-vinyl-and-22difluorovinyl-tosylates-via-the-suzukimiyaura-cross-coupling(99cf710d-2abc-41e2-aab8-b312a38c72d4).html
Akademický článek
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Publikováno v:
PMC
Nickel(0) catalysts have proven to be powerful tools for multicomponent coupling reactions in our laboratories over the past 15 years. This interest was originally sparked by the ubiquity of allylic alcohol motifs in natural products, such as (–)-t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aebd404aa93c440d06e17df59c4ae29e
https://orcid.org/0000-0002-8601-7799
https://orcid.org/0000-0002-8601-7799