Publikation: Asymmetric Synthesis of Enantiomerically Pure Phosphonic Analogues of Glutamic Acid and Proline
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1992
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Tetrahedron. 1992, 48(1), pp. 117-122. ISSN 0040-4020. Available under: doi: 10.1016/S0040-4020(01)80584-6
Zusammenfassung
Michael addition of the metallated camphor derivatives 2 to vinylogous esters and subsequential hydrolysis afforded phosphonic analogues of glutamic acid. The enantiomerically pure lactam 6 was reduced by LiBH4/BF3·OEt2 to phosphoproline 7.
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GROTH, Ulrich, Lutz RICHTER, Ulrich SCHÖLLKOPF, 1992. Asymmetric Synthesis of Enantiomerically Pure Phosphonic Analogues of Glutamic Acid and Proline. In: Tetrahedron. 1992, 48(1), pp. 117-122. ISSN 0040-4020. Available under: doi: 10.1016/S0040-4020(01)80584-6BibTex
@article{Groth1992Asymm-9985, year={1992}, doi={10.1016/S0040-4020(01)80584-6}, title={Asymmetric Synthesis of Enantiomerically Pure Phosphonic Analogues of Glutamic Acid and Proline}, number={1}, volume={48}, issn={0040-4020}, journal={Tetrahedron}, pages={117--122}, author={Groth, Ulrich and Richter, Lutz and Schöllkopf, Ulrich} }
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