AAAAAA

   
Results: 1-9 |
Results: 9
Improved treatment of cyclic beta-amino acids and successful prediction ofbeta-Peptide secondary structure using a modified force field: AMBERC
Authors: Christianson, LA Lucero, MJ Appella, DH Klein, DA Gellman, SH
Citation: La. Christianson et al., Improved treatment of cyclic beta-amino acids and successful prediction ofbeta-Peptide secondary structure using a modified force field: AMBERC, J COMPUT CH, 21(9), 2000, pp. 763-773
(R,R,R)-2,5-diaminocylohexanecarboxylic acid, a building block for water-soluble, helix-forming beta-peptides
Authors: Appella, DH LePlae, PR Raguse, TL Gellman, SH
Citation: Dh. Appella et al., (R,R,R)-2,5-diaminocylohexanecarboxylic acid, a building block for water-soluble, helix-forming beta-peptides, J ORG CHEM, 65(15), 2000, pp. 4766-4769
Synthesis of beta-alkyl cyclopentanones in high enantiomeric excess via copper-catalyzed asymmetric conjugate reduction
Authors: Moritani, Y Appella, DH Jurkauskas, V Buchwald, SL
Citation: Y. Moritani et al., Synthesis of beta-alkyl cyclopentanones in high enantiomeric excess via copper-catalyzed asymmetric conjugate reduction, J AM CHEM S, 122(28), 2000, pp. 6797-6798
Solution conformations of helix-forming beta-amino acid homooligomers
Authors: Barchi, JJ Huang, XL Appella, DH Christianson, LA Durell, SR Gellman, SH
Citation: Jj. Barchi et al., Solution conformations of helix-forming beta-amino acid homooligomers, J AM CHEM S, 122(12), 2000, pp. 2711-2718
Asymmetric conjugate reduction of alpha,beta-unsaturated esters using a chiral phosphine-copper catalyst
Authors: Appella, DH Moritani, Y Shintani, R Ferreira, EM Buchwald, SL
Citation: Dh. Appella et al., Asymmetric conjugate reduction of alpha,beta-unsaturated esters using a chiral phosphine-copper catalyst, J AM CHEM S, 121(40), 1999, pp. 9473-9474
Synthesis and structural characterization of helix-forming beta-peptides: trans-2-aminocyclopentanecarboxylic acid oligomers
Authors: Appella, DH Christianson, LA Klein, DA Richards, MR Powell, DR Gellman, SH
Citation: Dh. Appella et al., Synthesis and structural characterization of helix-forming beta-peptides: trans-2-aminocyclopentanecarboxylic acid oligomers, J AM CHEM S, 121(33), 1999, pp. 7574-7581
Synthesis and characterization of trans-2-aminocyclohexanecarboxylic acid oligomers: An unnatural helical secondary structure and implications for beta-peptide tertiary structure
Authors: Appella, DH Christianson, LA Karle, IL Powell, DR Gellman, SH
Citation: Dh. Appella et al., Synthesis and characterization of trans-2-aminocyclohexanecarboxylic acid oligomers: An unnatural helical secondary structure and implications for beta-peptide tertiary structure, J AM CHEM S, 121(26), 1999, pp. 6206-6212
Asymmetric hydrogenation of unfunctionalized tetrasubstituted olefins witha cationic zirconocene catalyst
Authors: Troutman, MV Appella, DH Buchwald, SL
Citation: Mv. Troutman et al., Asymmetric hydrogenation of unfunctionalized tetrasubstituted olefins witha cationic zirconocene catalyst, J AM CHEM S, 121(20), 1999, pp. 4916-4917
Formation of short, stable helices in aqueous solution by beta-amino acid hexamers
Authors: Appella, DH Barchi, JJ Durell, SR Gellman, SH
Citation: Dh. Appella et al., Formation of short, stable helices in aqueous solution by beta-amino acid hexamers, J AM CHEM S, 121(10), 1999, pp. 2309-2310
Risultati: 1-9 |