cheminform abstract: diastereoselective 1,3-dipolar cycloadditions with enantiopure azomethine ylids

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1998 pyrrole derivatives pyrrole derivatives R 0120 50 - 141 Diastereoselective 1,3-Dipolar Cycloadditions with Enantiopure Azomethine Ylids. A variety of highly functionalized diastereomer- ically pure pyrrolidines is synthesized via 1,3-dipolar cycloaddition of in situ prepared stabilized azomethine ylids to different dipolarophiles. — (ENDERS, D.; MEYER, I.; RUNSINK, J.; RAABE, G.; Tetrahedron 54 (1998) 36, 10733-10752; Inst. Org. Chem., RWTH Aachen, D-52074 Aachen, Germany; EN) 1

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Page 1: ChemInform Abstract: Diastereoselective 1,3-Dipolar Cycloadditions with Enantiopure Azomethine Ylids

1998 pyrrole derivatives

pyrrole derivativesR 0120

50 - 141Diastereoselective 1,3-Dipolar Cycloadditions with EnantiopureAzomethine Ylids. — A variety of highly functionalized diastereomer-ically pure pyrrolidines is synthesized via 1,3-dipolar cycloaddition of in situprepared stabilized azomethine ylids to different dipolarophiles. — (ENDERS,D.; MEYER, I.; RUNSINK, J.; RAABE, G.; Tetrahedron 54 (1998) 36,10733-10752; Inst. Org. Chem., RWTH Aachen, D-52074 Aachen, Germany;EN)

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Page 2: ChemInform Abstract: Diastereoselective 1,3-Dipolar Cycloadditions with Enantiopure Azomethine Ylids

1998 pyrrole derivatives

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