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Structural and conformational properties of phosphonylmethyl analogues of diribonucleoside monophosphates studied by Raman spectroscopy

✍ Scribed by P. Mojzeš; J. Štěpánek; I. Rosenberg; Z. Točík; M. Burian; M. Pavelčíková; M. Réfrégiers; H. Videlot


Publisher
Elsevier Science
Year
1995
Tongue
English
Weight
317 KB
Volume
348
Category
Article
ISSN
0022-2860

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## Abstract Acid–base properties of the natural polyamine wasp toxin PhTX‐433 (1) and seven synthetic analogues [PhTX‐343 (2), PhTX‐334 (3), PhTX‐443 (4), PhTX‐434 (5), PhTX‐344 (6), PhTX‐444 (7), and PhTX‐333 (8)], each having four protolytic sites, were characterized by ^13^C NMR spectroscopy. No