@article{ref1,
title="Synthesis of a potential "suicide substrate" of the HIV-1 protease, incorporating A 3-acetoxy-Δ-4,5-(L)-pipecolic acid as proline substitute",
journal="Tetrahedron Letters",
year="1992",
author="Mazaleyrat, J.-p. and Rage, I. and Xie, J. and Savrda, J. and Wakselman, M.",
volume="33",
number="31",
pages="4453-4456",
abstract="Coupling of (D,L)-baikiain methyl ester with Boc-(L)-phenylalanine, followed by saponification, idolactonization and aminolysis of the diastereoisomeric iodolactones by (L)-isoleucyl-(L)-valine methyl ester gave two diastereoisomeric peptides incorporating either a 3S-hydroxy-4S-iodo-(L)-pipecolic acid or a 3R-hydroxy-4R-iodo-(D)-pipecolic acid residue, which were separated by thin layer chromatography. Assignment of configuration was unambiguous when the synthesis was repeated with (L)-baikiain as starting material. All compounds exhibited conformational isomerism in their1H NMR spectra, attributed to the existence of boths-cis ands-trans configurations of the Phe-NR2 peptide bond. Acetylation of each of the two separated diastereoisomers gave Boc-(L)-Phe-3S-OAc-4S-I-(L)-Pip-(L)-Ile-(L)-Val-OMe and Boc-(L)-Phe-3R-OAc-4R-I-(D)-Pip-(L)-Ile-(L)-Val-OMe. N-deprotection and coupling of the former with Boc-(L)-Ser-(L)-Ala-(L)-Ala-OH by the DCC/HOBt method or stepwise elongation of the peptidic chain, gave Boc-(L)-Ser-(L)-Ala-(L)-Ala-(L)-Phe-3S-OAc-4S-I-(L)-Pip-(L)-Ile-(L)-Val-OMe. Dehydroiodination of this compound on treatment with DBU gave Boc-(L)-Ser-(L)-Ala-(L)-Ala-(L)-Phe-3S-OAc-Δ-4,5-(L)-Pip-(L)-Ile-(L)-Val-OMe, a potential &quot;suicide substrate&quot; of the HIV-1 protease. © 1992 Pergamon Press Ltd.<p /><p>Language: en</p>",
language="en",
issn="0040-4039",
doi="10.1016/S0040-4039(00)60108-9",
url="http://dx.doi.org/10.1016/S0040-4039(00)60108-9"
}