Helvetica chimica acta

Pteridines, part CXIII

Q Yao, W Pfleiderer

Index: Yao, Qizheng; Pfleiderer, Wolfgang Helvetica Chimica Acta, 2003 , vol. 86, # 1 p. 1 - 12

Full Text: HTML

Citation Number: 16

Abstract

Abstract The low solubility of pterins can drastically be improved by N 2-acylation or formation of the N 2-[(dimethylamino) methylene] derivatives. Both types of compounds can be alkylated under Mitsunobu conditions to form from N 2-acylpterins (see 2 and 3) and their

Related Articles:

Phosphinic acid pseudopeptides analogous to glutamyl-γ-glutamate: synthesis and coupling to pteroyl azides leads to potent inhibitors of folylpoly-γ-glutamate …

[Valiaeva; Bartley; Konno; Coward Journal of Organic Chemistry, 2001 , vol. 66, # 15 p. 5146 - 5154]

Pteridines, part CXIII

[Helvetica Chimica Acta, , vol. 86, # 1 p. 1 - 12]

Pteridines, part CXIII

[Helvetica Chimica Acta, , vol. 86, # 1 p. 1 - 12]

Synthesis of tritiated N??[4??(2, 4??diaminopteridine??6??methyl)??3, 4??dihydro??2H??1, 4??benzothiazine??7??carbonyl]??L??homo glutamic acid (MX??68)

[Journal of Labelled Compounds and Radiopharmaceuticals, , vol. 39, # 5 p. 363 - 368]

Synthesis of tritiated N??[4??(2, 4??diaminopteridine??6??methyl)??3, 4??dihydro??2H??1, 4??benzothiazine??7??carbonyl]??L??homo glutamic acid (MX??68)

[Journal of Labelled Compounds and Radiopharmaceuticals, , vol. 39, # 5 p. 363 - 368]

More Articles...