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https://www.researchgate.net/publication/230374377_Asymmetric_Organocatalytic_Diels-Alder_Reactions_on_Solid_Support
Asymmetric Organocatalytic Diels–Alder Reactions on Solid Support Article in Advanced Synthesis & Catalysis 344(9):941 - 945 · October 2002 with 77 Reads How we measure 'reads'
https://pubs.acs.org/doi/abs/10.1021/ja054008q
Jul 28, 2005 · The first direct enantioselective organocatalytic intramolecular Diels−Alder reaction has been accomplished. The use of iminium catalysis has provided a new catalytic strategy for the enantioselective [4 + 2] cycloisomerization of a wide variety of tethered diene-enal systems. The use of imidazolidinones 1 and 2 as the asymmetric catalysts has been found to mediate the enantioselective ...Cited by: 247
https://pubs.acs.org/doi/abs/10.1021/cr00013a013
Chiral Catalyst Optimization Using Both Solid-Phase and Liquid-Phase Methods in Asymmetric Aza Diels−Alder Reactions. ... The First Highly Enantioselective Organocatalytic Diels−Alder Reaction. Journal of the American Chemical Society 2000, 122 ... Asymmetric Diels−Alder Reactions of Chiral 1-Amino-3-siloxy-1,3-butadiene: Application to ...Cited by: 938
https://www.researchgate.net/publication/224045683_Enantioselective_Organocatalytic_Diels-Alder_Reactions
Enantioselective organocatalytic asymmetric Diels-Alder reactions provide a facile and efficient route to optically active functionalized cyclohexenes, which can be further transformed into a ...
https://aaltodoc.aalto.fi/handle/123456789/22428
Citation: Selkälä , S A , Tois , J , Pihko , P M & Koskinen , A M P 2002 , ' Asymmetric Organocatalytic Diels-Alder Reactions on Solid Support ' ADVANCED SYNTHESIS AND CATALYSIS , vol 344 , …Cited by: 142
https://www.deepdyve.com/lp/wiley/asymmetric-organocatalytic-diels-alder-reactions-on-solid-support-869FhFkvo0
Oct 01, 2002 · Asymmetric organocatalysis on solid support combines the environmental advantages of metal‐free catalysts and the ease of operation of solid‐supported reagents. Enantioselective organocatalytic Diels Alder reactions have been demonstrated by two different solid‐supported chiral organocatalysts. The catalysts are easy to recover and they can be reused. The reactivity of the …
http://onlinelibrary.wiley.com/doi/10.1002/anie.200804275/full
Diels or no Diels? A bifunctional organic catalyst based on the thiourea motif is able to coordinate both diene and dienophile in an unprecedented asymmetric Diels–Alder reaction of 3‐vinylindole derivatives, giving a rapid access to optically active tetra‐ and hexahydrocarbazoles with excellent results in terms of yields, diastereoselectivities, and enantioselectivities.
https://core.ac.uk/display/80721260
Asymmetric organocatalysis on solid support combines the environmental advantages of metal-free catalysts and the ease of operation of solid-supported reagents. Enantioselective organocatalytic DielsAlder reactions have been demonstrated by two different solid-supported chiral organocatalysts. The catalysts are easy to recover and they can be ...
http://onlinelibrary.wiley.com/doi/10.1002/anie.200351916/full
A practical and environmentally friendly organocatalytic process for the synthesis of optically active highly substituted spiro[5,5]undecane‐1,5,9‐triones was achieved through the reaction of an aldehyde, an enone, and Meldrum's acid in the presence of a catalytic amount of chiral amino acid (see scheme). The Diels–Alder products were obtained as single diastereomers in excellent yields ...
https://application.wiley-vch.de/books/sample/3527320881_c01.pdf
1 Asymmetric Catalysis of Diels–Alder Reaction Haifeng Du and Kuiling Ding 1.1 Introduction The Diels–Alder (DA) reaction (or diene synthesis ) between a diene and a dienophile generates two s bonds stereoselectively and up to four chiral centers in a single step to afford six-membered cyclic compounds. This cycloaddition
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