356
ORGANIC SYNTHESIS—1995
VI.A.7-15 Reetz, M.T. et al., TU 35, 8765; Utimoto, K. et al., CU 827.
* * S
Et
Me 3 SiNHOSiMe 3 ^ ^
j * * *
C0 2 Et
CH2C
'
2
'
ft
^ R^Y^C0 2 Et
NHOSiMe 3
60-76 %, major isomer
VI.A.7-16 Pascal, R. et al., TU 35, 6291.
Carboxyl-Protecting Groups Convertible into Activating Groups.
Carbamates of o-Aminoanilides are Precursors of Reactive NAcylureas.
VI.A.7-17 DeGrado, W. et al., TU 35, 6191.
A General Method for Coupling Unprotected Peptides to
Bromoacetamido Porphyrin Templates.
VI.A.7-18 Rich, D.H. et al., TU 35, 5981.
Comparative Studies of the Coupling of N-Methylated, Sterically
Hindered Amino Acids During Solid-Phase Peptide Synthesis.
VI.A.7-19 Jezek, J. and Houghten, R.A., CCC, 59, 691.
A Comparative Study of BOP as a Coupling Agent Using
Simultaneous Multiple Peptide Synthesis.
VI.A.7-20 Hoffmann, S. and Frank, R., TU 35, 7763.
A New Safety-Catch Peptide-Resin Linkage for the Direct Release
of Peptides into Aqueous Buffers.
ORGANIC SYNTHESIS—1995
VI.A.7-15 Reetz, M.T. et al., TU 35, 8765; Utimoto, K. et al., CU 827.
* * S
Et
Me 3 SiNHOSiMe 3 ^ ^
j * * *
C0 2 Et
CH2C
'
2
'
ft
^ R^Y^C0 2 Et
NHOSiMe 3
60-76 %, major isomer
VI.A.7-16 Pascal, R. et al., TU 35, 6291.
Carboxyl-Protecting Groups Convertible into Activating Groups.
Carbamates of o-Aminoanilides are Precursors of Reactive NAcylureas.
VI.A.7-17 DeGrado, W. et al., TU 35, 6191.
A General Method for Coupling Unprotected Peptides to
Bromoacetamido Porphyrin Templates.
VI.A.7-18 Rich, D.H. et al., TU 35, 5981.
Comparative Studies of the Coupling of N-Methylated, Sterically
Hindered Amino Acids During Solid-Phase Peptide Synthesis.
VI.A.7-19 Jezek, J. and Houghten, R.A., CCC, 59, 691.
A Comparative Study of BOP as a Coupling Agent Using
Simultaneous Multiple Peptide Synthesis.
VI.A.7-20 Hoffmann, S. and Frank, R., TU 35, 7763.
A New Safety-Catch Peptide-Resin Linkage for the Direct Release
of Peptides into Aqueous Buffers.