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Organocascade catalysis

SCHEME 6.5. Natural product synthesis through Diels-Alder based organocascade catalysis. [Pg.210]

MacMillan and co-workers demonstrated the capabilities of collective total synthesis in combination with organocascade catalysis very recently [53], which provided them a new synthetic strategy to achieve large collections of complex molecular architectures from a common molecular scaffold [54]. The power of this... [Pg.602]

We categorized the organocascade catalysis into a separated section as more and more organocatalysts have been used as a single catalyst or co-catalyst in various... [Pg.618]

Jones SB, Simmons B, Mastracchio A, MacMillan DWC (2011) Collective Synthesis of Natural Products by Means of Organocascade Catalysis. Nature 475 183... [Pg.154]

Simmons B, Walji AM, MacMillan DWC (2009) Cycle-Specific Organocascade Catalysis Application to Olefin Hydroamination, Hydro-oxidation, and Amino-oxidation, and to Natural Product Synthesis. Angew Chem Int Ed 48 4349... [Pg.154]

Jones, S. B., Simmons, B., Mastracchio, A., MacMillan, D. W. C. 2011. Collective synthesis of natural products by means of organocascade catalysis. Nature 475 183-188. [Pg.344]

SCHEME 2.29 Organocascade catalysis with combination of azodicarboxylate and either indole or thiol derivatives. [Pg.32]

Bencivenni, G., Wu, L.-Y., Mazzanti, A., Giannichi, B., Pesciaioli, R, Song, M.-R, Bar-toli, G., Melchiorre P. (2009). Targeting structural and stereochemical complexity by organocascade catalysis construction of spirocyclic oxindoles having multiple stereocenters. Angewandte Chemie International Edition, 48, 7200-7203. [Pg.303]

Scheme 12.11 Organocascade catalysis with a,(3-disubstituted enals, indole, and azodicar-boxylate. Scheme 12.11 Organocascade catalysis with a,(3-disubstituted enals, indole, and azodicar-boxylate.
Simmons, B., Walji, A. M., Mac Millan, D. W. C. (2009). Cycle-specific organocascade catalysis appheation to olefin hydroamination, hydro-oxidation and amino-oxidation and to natural product synthesis. Angewandte Chemie International Edition, 48,4349-4353. [Pg.360]

The first example of dual organocascade catalysis involving iminium/enamine activation was published in 2005 (Scheme 35.15) [6]. In this report, a, 3-unsaturated... [Pg.1053]

Organocascade Catalysis Combinations of Enamine and Iminium Catalysis [55]... [Pg.1365]

Simmons B, Walji AM, MacMillan DWC. Cycle-specific organocascade catalysis application to olefin hydroamina-tion, hydro-oxidation, and amino-oxidation, and to natural product synthesis. Angew. Chem. Int. Ed. 2009 48(24) 4349-4353. [Pg.345]


See other pages where Organocascade catalysis is mentioned: [Pg.618]    [Pg.619]    [Pg.619]    [Pg.35]    [Pg.209]    [Pg.347]    [Pg.1053]    [Pg.1365]    [Pg.1406]    [Pg.1413]    [Pg.1421]    [Pg.130]    [Pg.610]    [Pg.1053]    [Pg.1365]   
See also in sourсe #XX -- [ Pg.1365 ]




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Enamine organocascade catalysis

Enantioselective Organocascade Catalysis

Iminium organocascade catalysis

Organocascade catalysis, combined

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