C-acylations of polymeric phosphoranylidene acetates for C-terminal variation of peptide carboxylic acids.
Adeeb El-Dahshan, Steffen Weik, Jörg Rademann
Index: Org. Lett. 9(6) , 949-52, (2007)
Full Text: HTML
Abstract
C-Acylations of polymer-supported 2-phosphoranylidene acetates ("linker reagents") with protected amino acids yielded 2-acyl-2-phosphoranylidene acetates as flexible intermediates for the C-terminal variation of carboxylic acids: peptidyl-2,3-diketoesters, peptidyl vinyl ketones, peptidyl-2-ketoaldehydes, and 1,3-diamino-2-hydroxy-propanes were obtained as products. [reaction: see text]
Related Compounds
Related Articles:
Streptomyces maoxianensis sp. nov., a novel actinomycete isolated from soil in Maoxian, China.
2015-05-01
[Antonie van Leeuwenhoek 107(5) , 1119-26, (2015)]
2015-04-15
[Vet. Immunol. Immunopathol. 164 , 101-9, (2015)]
2015-09-01
[Mol. Med. Report. 12 , 4669-77, (2015)]
Host-like carbohydrates promote bloodstream survival of Vibrio vulnificus in vivo.
2015-08-01
[Infect. Immun. 83 , 3126-36, (2015)]
Polymer complex of WR 2721. Synthesis and radioprotective efficiency.
2014-12-18
[Eur. J. Pharm. Sci. 65 , 9-14, (2014)]