scholarly journals Amino acids and peptides. IX. Synthetic studies on Leu-enkephalin analogues containing a ureylene bond.

1988 ◽  
Vol 36 (5) ◽  
pp. 1766-1771 ◽  
Author(s):  
KOICHI KAWASAKI ◽  
MITSUKO MAEDA ◽  
JOE WATANABE ◽  
HIROSHI KANETO
1998 ◽  
Vol 33 (4) ◽  
pp. 331-334 ◽  
Author(s):  
Irina Bobrova ◽  
Natalia Mishlakova ◽  
Anette Selander ◽  
Elena Mekshun ◽  
Guntis Rozental

1989 ◽  
Vol 37 (3) ◽  
pp. 826-828 ◽  
Author(s):  
Mitsuko MAEDA ◽  
Koichi KAWASAKI ◽  
Joe WATANABE ◽  
Hiroshi KANETO

2001 ◽  
Vol 79 (11) ◽  
pp. 1632-1654 ◽  
Author(s):  
Richard R Hark ◽  
Diane B Hauze ◽  
Olga Petrovskaia ◽  
Madeleine M Joullié

Ninhydrin is an essential tool in the analysis of amino acids, peptides, and proteins, and the preferred reagent for the detection of latent fingerprints on porous surfaces. The goal of this investigation was to prepare ninhydrin analogs with enhanced chromogenic and fluorogenic properties. Target compounds included structures with extended conjugation and (or) with the presence of sulfur-containing moieties. We have devised general convergent routes for novel heterocyclic and aryl-substituted ninhydrin analogs for use as reagents for amino acid detection.Key words: ninhydrin analogs, synthesis, ketals, Suzuki cross-coupling reactions, Stille cross-coupling reactions.


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