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Antibiotics - Nonhaemolytic beta-amino-acid oligomers
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Porter, E.A.1
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Gellman, S.H.5
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4
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0037134881
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Tolerance of acyclic residues in the β-peptide 12-helix: Access to diverse side-chain arrays for biological applications
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(b) LePlae, P. R.; Fisk, J. D.; Porter, E. A.; Weisblum, B.; Gellman, S. H. Tolerance of acyclic residues in the β-peptide 12-helix: Access to diverse side-chain arrays for biological applications. J. Am. Chem. Soc. 2002, 124, 6820-6821;
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β-Amino acids: Versatile peptidomimetics
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(b) Liu, M.; Sibi, M. P. Recent advances in the stereoselective synthesis of β-amino acids. Tetrahedron 2002, 58, 7991-8035;
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Liu, M.1
Sibi, M.P.2
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Convenient preparation of tert-butyl β-(protected amino)esters
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(a) Katritzky, A. R.; Kirichenko, K.; Elsayed, A. M.; Ji, Y.; Fang, Y. Convenient preparation of tert-butyl β-(protected amino)esters. J. Org. Chem. 2002, 67, 4957-4959;
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Ji, Y.4
Fang, Y.5
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11
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N-(1-Benzotriazol-1-ylalkyl)amides, versatile α-amidoalkylation reagents, 1: α-amidoalkylation of CH acids
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(b) Katritzky, A. R.; Pernak, J.; Fan, W.-Q.; Saczewski, F. N-(1-Benzotriazol-1-ylalkyl)amides, versatile α-amidoalkylation reagents, 1: α-amidoalkylation of CH acids J. Org. Chem. 1991, 56, 4439-4443.
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Katritzky, A.R.1
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Reaction of α-amidoalkylphenyl sulfones with Reformatsky reagents. A new entry to β-amino esters
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(a) Mecozzi, T.; Petrini, M. Reaction of α-amidoalkylphenyl sulfones with Reformatsky reagents. A new entry to β-amino esters. Tetrahedron Lett. 2000, 41, 2709-2712;
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Mecozzi, T.1
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A convenient synthesis of N-Boc-protected α-aminonitriles from α-amidosulfones
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For our previous related work concerning a synthesis of α-amino acids from α-amido sulfones; see Banphavichit, V.; Chaleawlertumpon, S.; Bhanthumnavin, W.; Vilaivan, T. A convenient synthesis of N-Boc-protected α-aminonitriles from α-amidosulfones. Synth. Commun. 2004, 34, 3147-3160.
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Chaleawlertumpon, S.2
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Vilaivan, T.4
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Synthesis of beta-aryl-beta-amino-ethane-alpha, alpha-dicarbonic acids: The mechanism of Knoevenagel's synthesis of cinnamic acids
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A one-pot synthesis of 3-amino-3-arylpropionic acids
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Sodium and potassium carbonates: Efficient strong bases in solid-liquid two-phase systems
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19
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Highly stereocontrolled and efficient preparation of the protected, esterification-ready docetaxel (taxotere) side chain
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Kanazawa, A. M.; Denis, J.-N.; Greene, A. E. Highly stereocontrolled and efficient preparation of the protected, esterification-ready docetaxel (taxotere) side chain. J. Org. Chem. 1994, 59, 1238-1240.
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