Photochemistry of N-phthaloyl derivatives of electron-donor-substituted amino acids
…, J Hirt, V Ptatschek, T Engel, D Löffler, FW Schneider
Index: Griesbeck; Henz; Hirt; Ptatschek; Engel; Loffler; Schneider Tetrahedron, 1994 , vol. 50, # 3 p. 701 - 714
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Citation Number: 34
Abstract
The hydroxy substituted amino acids threonine and serine have been investigated concerning their photochemical behaviour when activated as N-phthaloyl substrates. The methyl esters 1a and 2a solely underwent cleavage of the central C C single bond to give the glycine derivative 3 and an aldehyde fragment. C-unprotected threonine derivative 1b is converted into a series of products the composition of which depends on solvent polarity ...
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