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Synlett 1999; 1999(12): 1903-1906
DOI: 10.1055/s-1999-3176
DOI: 10.1055/s-1999-3176
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Synthesis of 2-Amino-2-methyl-4-phosphonobutanoic Acids by Conjugate Addition of Lithiated Bislactim Ether Derived from Cyclo[Ala-d-Val] to Vinylphosphonates
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Publikationsdatum:
31. Dezember 1999 (online)
![](https://www.thieme-connect.de/media/synlett/199912/lookinside/thumbnails/10.1055-s-1999-3176-1.jpg)
Face-selective conjugate addition of lithiated Schöllkopf's bislactim ether derived from cyclo[Ala-d-Val] 4 to prochiral vinylphosphonates 5a-c allows a direct and stereocontrolled access to optically pure MAP4 analogues, the 2-amino-2-methyl-4-phosphonobutanoic acid derivatives 12-15. The relative stereochemistry was assigned from NMR studies of the cyclic derivatives 16 and 17. Eight-membered transition states are invoked to rationalize the stereochemical outcome of the additions.
phosphonobutanoic acids - α-methyl α-amino acids - conjugate addition - stereoselective synthesis - vinylphosphonates