Enantioselective solvent-free Robinson annulation reactions
نویسندگان
چکیده
منابع مشابه
Antibody-Catalyzed Enantioselective Robinson Annulation
We report an antibody that is remarkable in that it catalyzes both steps of an important synthetic transformation, the Robinson annulation. The Robinson annulation which accomplishes, in net terms, the conversion of a f c occupies a key role in organic synthesis.1 In most instances, the overall annulation is comprised of an alkylation (or Michael addition) step leading to b followed by a cyclod...
متن کاملEnantioselective synthesis of the ABC ring motif of norzoanthamine based on asymmetric Robinson annulation reactions.
An enantioselective strategy for the synthesis of tetracyclic motif 5, representing the northern fragment of norzoanthamine, is presented. Key to the strategy is the use of two asymmetric Robinson annulation reactions that produce the tricyclic ABC ring system with excellent stereoselectivity. Further functionalization at the periphery of the C ring produces compound 5 containing six contiguous...
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Controlled isomerization of the double bond of certain Diels-Alder reactions provides substrates that, upon oxidation, give rise to products whose gross structure corresponds to that of a Robinson annulation. In these cases, the stereochemistry of the Robinson annulation product reflects the fact that the initial combination occurred in a Diels-Alder mode. Using these principles, we have synthe...
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An efficient method to synthesis the 2H-pyrans using three component reactions of dithiocarbamats, activated acetylenes and isocyanides in water as the solvent is described. In these reactions, synthesis of 2H-pyrans is possible based on the one-pot reaction and without using any catalyst. The mild reaction conditions and high yields of the products exhibit synthetic advantage of these methods.
متن کاملSolvent-free Substitution Reactions of Solid Phosphines
Reactions of (η-RC5H4)Fe(CO)2I (R = H, Me) complexes with phosphine ligands PR′3 (R′ = Ph, m-Tol, p-C6H4OMe, p-C6H4Cl, p-C6H4F) have been performed under solvent-free conditions in the melt phase and generally yielded the ionic products [(η5-RC5H4)Fe(CO)2PR′3]I rather than the CO substituted products (η5-RC5H4)Fe(CO)(PR′3)I. The complexes have been characterised by IR, NMR and MS techniques. By...
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ژورنال
عنوان ژورنال: Journal of Chemical Sciences
سال: 2001
ISSN: 0253-4134,0973-7103
DOI: 10.1007/bf02704070