Efficient synthesis of unnatural dipeptides based on cis-2,5-disubstituted pyrrolidine
Author:
Publisher
Springer Science and Business Media LLC
Subject
Organic Chemistry,Clinical Biochemistry,Biochemistry
Link
http://link.springer.com/content/pdf/10.1007/s00726-011-0949-4.pdf
Reference34 articles.
1. Bagley MC, Tovey J (2001) Diastereoselective synthesis of cis-2,5-disubstituted pyrrolidine N-oxides by the retro-Cope elimination. Tetrahedron Lett 42:351–353
2. Brenneman JB, Martin SF (2004) Application of intramolecular enyne metathesis to the synthesis of aza[4.2.1]bicyclics: enantiospecific total synthesis of (+)-Anatoxin-a. Org Lett 6:1329–1331
3. Cahill JP, Cunneen D, Guiry PJ (1999) trans-2,5-Dialkylpyrrolidinyl-containing phosphinamines. Synthetic and mechanistic studies in Pd-catalysed asymmetric allylic alkylation. Tetrahedron Asymmetry 10:4157–4173
4. Chen HF, Sweet JA, Lam KC, Rheingold AL, McGrath DV (2009) Chiral amine–imine ligands based on trans-2,5-disubstituted pyrrolidines and their application in the palladium-catalyzed allylic alkylation. Tetrahedron Asymmetry 20:1672–1682
5. Colandrea VJ, Legiec IE, Huo P, Yan L et al (2006) 2,5-Disubstituted pyrrolidine carboxylates as potent, orally active sphingosine-1-phosphate (S1P) receptor agonists. Bioorg Med Chem Lett 16:2905–2908
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