Intramolecular n-alkenylnitrone-additions: regio- and stereochemistry

Article Article scientifique Article Intramolecular n-alkenylnitrone-additions: regio- and stereochemistry eng 1985 author Von Oppolzer Wolfgang 25270 author Siles Alvarado Samuel author Snowden Roger 28308 author Bakker Bartholomeus Hendrieus 63154 author Petrzilka Benjamin Martin 592949 3497-3509 10.1016/S0040-4020(01)96703-1 0040-4020 https://linkinghub.elsevier.com/retrieve/pii/S0040402001967031 Efficient intramolecular cycloadditions of N-3-alkenyl- and N-4-alkenylnitrones proceed with opposite regioselection which is modified by dipolarophile-substituent effects. Polycyclic isoxazolidines are obtained in a highly stereocontrolled fashion, consistent with an endo-addition of the Z-nitrones. Dewey 540 36 Département de chimie organique 141 false Tetrahedron 41 17 91fb23b7-5d70-46ee-adfe-a2b591b15537 Article (Published version) Restricted Oppolzer_T_1985413497.pdf 8501317 application/pdf b50d113ee00890f18bea3bbbd70b40dd8f96150f95286396d452ca614b4ede3d restrictedAccess Faculté des sciences / Section de chimie et biochimie / Département de chimie organique

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Intramolecular n-alkenylnitrone-additions: regio- and stereochemistry	Tetrahedron			1985	81	0

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Petrzilka, Benjamin Martin