Conformationally constrained dipeptide surrogates with aromatic side-chains: Synthesis of 4-aryl indolizidin-9-one amino acids by conjugate addition to a common α, ω-diaminoazelate enone intermediateCLUZEAU, Jérome; LUBELL, William D.Journal of organic chemistry. 2004, Vol 69, Num 5, pp 1504-1512, issn 0022-3263, 9 p.Article

Efficient synthesis of enantiopure pyrrolizidinone amino acidDIETRICH, Evelyne; LUBELL, William D.Journal of organic chemistry. 2003, Vol 68, Num 18, pp 6988-6996, issn 0022-3263, 9 p.Article

Aza-1,2,3-triazole-3-alanine Synthesis via Copper-Catalyzed 1,3-Dipolar Cycloaddition on Aza-progargylglycinePROULX, Caroline; LUBELL, William D.Journal of organic chemistry. 2010, Vol 75, Num 15, pp 5385-5387, issn 0022-3263, 3 p.Article

9-(4-Bromophenyl)-9-fluorenyl as a safety-catch nitrogen protecting groupSURPRENANT, Simon; LUBELL, William D.Journal of organic chemistry. 2006, Vol 71, Num 2, pp 848-851, issn 0022-3263, 4 p.Article

Conformationally constrained dipeptide surrogates with aromatic side-chains : synthesis of 4-aryl indolizidin-9-one amino acids by conjugate addition to a common α,ω-diaminoazelate enone intermediateCLUZEAU, Jérome; LUBELL, William D.Journal of organic chemistry. 2004, Vol 69, Num 5, pp 1504-1512, issn 0022-3263, 9 p.Article

Synthesis of fused heteroarylprolines and pyrrolopyrrolesJEANNOTTE, Guillaume; LUBELL, William D.Journal of organic chemistry. 2004, Vol 69, Num 14, pp 4656-4662, issn 0022-3263, 7 p.Article

Large structural modification with conserved conformation: Analysis of Δ³-fused aryl prolines in model β-turnsJEANNOTTE, Guillaume; LUBELL, William D.Journal of the American Chemical Society. 2004, Vol 126, Num 44, pp 14334-14335, issn 0002-7863, 2 p.Article

Effect of sequence on peptide geometry in 5-tert-butylprolyl type VI β-turn mimicsHALAB, Liliane; LUBELL, William D.Journal of the American Chemical Society. 2002, Vol 124, Num 11, pp 2474-2484, issn 0002-7863Article

Mimics of Peptide Turn Backbone and Side-Chain Geometry by a General Approach for Modifying Azabicyclo[5.3.0]alkanone Amino AcidsGODINA, Tanya A; LUBELL, William D.Journal of organic chemistry. 2011, Vol 76, Num 14, pp 5846-5849, issn 0022-3263, 4 p.Article

β,β-Disubstituted C- and N-Vinylindoles from One-Step Condensations of Aldehydes and Indole DerivativesFRIDKIN, Gil; BOUTARD, Nicolas; LUBELL, William D et al.Journal of organic chemistry. 2009, Vol 74, Num 15, pp 5603-5606, issn 0022-3263, 4 p.Article

Aza-amino acid scan for rapid identification of secondary structure based on the application of N-Boc-aza¹-dipeptides in peptide synthesisMELENDEZ, Rosa E; LUBELL, William D.Journal of the American Chemical Society. 2004, Vol 126, Num 21, pp 6759-6764, issn 0002-7863, 6 p.Article

Synthesis and peptide coupling of protected 2-pyrrolylalanineDÖRR, Aurélie A; LUBELL, William D.Tetrahedron letters. 2011, Vol 52, Num 17, issn 0040-4039, 2014, 2159-2161 [4 p.]Article

Synthesis of Protected 2-Pyrrolylalanine for Peptide Chemistry and Examination of Its Influence on Prolyl Amide Isomer EquilibriumDÖRR, Aurélie A; LUBELL, William D.Journal of organic chemistry. 2012, Vol 77, Num 15, pp 6414-6422, issn 0022-3263, 9 p.Article

1,3,5-trisubstituted 1,4-diazepin-2-onesIDEN, Hassan S; LUBELL, William D.Journal of organic chemistry. 2007, Vol 72, Num 23, pp 8980-8983, issn 0022-3263, 4 p.Article

Serine as chiral educt for the practical synthesis of enantiopure N-protected β-hydroxyvalineDETTWILER, James E; LUBELL, William D.Journal of organic chemistry. 2003, Vol 68, Num 1, pp 177-179, issn 0022-3263, 3 p.Article

Systematic study of the synthesis of macrocyclic dipeptide β-turn mimics possessing 8-, 9-, and 10- membered rings by ring-closing metathesisKAUL, Ramesh; SURPRENANT, Simon; LUBELL, William D et al.Journal of organic chemistry. 2005, Vol 70, Num 10, pp 3838-3844, issn 0022-3263, 7 p.Article

Cyclic Aza-peptide Integrin Ligand Synthesis and Biological ActivitySPIEGEL, Jochen; MAS-MORUNO, Carlos; KESSLER, Horst et al.Journal of organic chemistry. 2012, Vol 77, Num 12, pp 5271-5278, issn 0022-3263, 8 p.Article

Diversity-oriented synthesis of functionalized pyrrolo[3,2-d]pyrimidines with variation of the pyrimidine ring nitrogen substituentsMARCOTTE, Félix-Antoine; ROMBOUTS, Frederik J. R; LUBELL, William D et al.Journal of organic chemistry. 2003, Vol 68, Num 18, pp 6984-6987, issn 0022-3263, 4 p.Article

Pyrrolo[3,2-e][1,4]diazepin-2-one Synthesis: A Head-to-Head Comparison of Soluble versus Insoluble SupportsBOUTARD, Nicolas; DUFOUR-GALLANT, Julien; DEAUDELIN, Philippe et al.Journal of organic chemistry. 2011, Vol 76, Num 11, pp 4533-4545, issn 0022-3263, 13 p.Article

Rigid dipeptide mimics : Synthesis of enantiopure C6-functionalized pyrrolizidinone amino acidsRAMANA RAO, Mallem H. V; PINYOL, Eulalia; LUBELL, William D et al.Journal of organic chemistry. 2007, Vol 72, Num 3, pp 736-743, issn 0022-3263, 8 p.Article

Fluorometric assay for tissue transglutaminase-mediated transamidation activityGNACCARINI, Claudio; BEN-TAHAR, Wajih; LUBELL, William D et al.Bioorganic & medicinal chemistry. 2009, Vol 17, Num 17, pp 6354-6359, issn 0968-0896, 6 p.Article

Bis(pyrrol-2-yl)arylenes from the tandem bidirectional addition of vinyl grignard reagent to aryl diestersHANSFORD, Karl A; PEREZ GUARIN, Sergio Andres; SKENE, W. G et al.Journal of organic chemistry. 2005, Vol 70, Num 20, pp 7996-8000, issn 0022-3263, 5 p.Article

Cinnamoyl Inhibitors of Tissue TransglutaminasePARDIN, Christophe; PELLETIER, Joelle N; LUBELL, William D et al.Journal of organic chemistry. 2008, Vol 73, Num 15, pp 5766-5775, issn 0022-3263, 10 p.Article

Unsymmetric Electronic Push—Pull Bipyrroles — Synthesis, Spectroelectrochemical, and Photophysical InvestigationTSHIBAKA, Tshitundu; ULLIEL ROCHE, Ivan; DUFRESNE, Stéphane et al.Journal of organic chemistry. 2009, Vol 74, Num 24, pp 9497-9500, issn 0022-3263, 4 p.Article

Selective tert-butyl ester deprotection in the presence of acid labile protecting groups with use of ZnBr₂KAUL, Ramesh; BROUILLETTE, Yann; SAJJADI, Zohreh et al.Journal of organic chemistry. 2004, Vol 69, Num 18, pp 6131-6133, issn 0022-3263, 3 p.Article