The stereoselective construction of the D-erythro-azidosphingosine characteristic trans double bond was accomplished by condensation between tetradecanal and a heterocyclic sulfone derived from diethyl-D-tartrate, following the Kocienski modification of the Julia olefination. © 2002 Elsevier Science Ltd. All rights reserved.
Compostella, F., Franchini, L., Panza, L., Prosperi, D., Ronchetti, F. (2002). A formal synthesis of 3-O-(4-methoxybenzyl)-azidosphingosine by a modified Julia olefination. TETRAHEDRON, 58(22), 4425-4428 [10.1016/S0040-4020(02)00418-0].
A formal synthesis of 3-O-(4-methoxybenzyl)-azidosphingosine by a modified Julia olefination
PROSPERI, DAVIDE;
2002
Abstract
The stereoselective construction of the D-erythro-azidosphingosine characteristic trans double bond was accomplished by condensation between tetradecanal and a heterocyclic sulfone derived from diethyl-D-tartrate, following the Kocienski modification of the Julia olefination. © 2002 Elsevier Science Ltd. All rights reserved.
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