Synthesis of novel optically active cyclic phospholipid conjugates of tegafur and uridine starting from L-serine

Article abstract of DOI:10.1080/00397910008087103

Starting from L-serine, cyclic phospholids 2,3 and 4 were synthesized and successfully separated in the form of pure diastereomer. Their configurations were discussed and assigned according to their NMR spectra data. The asymmetric induction effects were

Full text of DOI:10.1080/00397910008087103

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Synthetic Communications: An
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Organic Chemistry
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Synthesis of Novel Optically
Active Cyclic Phospholipid
Conjugates of Tegafur and
Uridine Starting From L-Serine
Zheng-Jie He a , Wen-Bin Chen a , Cheng-Xiang
Zhang a , Zheng-Hong Zhou a & Chu-Chi Tang a
a The State Key Laboratory of Elemento-Organic
Chemistry, Institute of Elemento-Organic Chemistry,
Nankai University , Tianjin, 300071, P. R. China
Published online: 04 Dec 2007.
To cite this article: Zheng-Jie He , Wen-Bin Chen , Cheng-Xiang Zhang , Zheng-Hong
Zhou & Chu-Chi Tang (2000) Synthesis of Novel Optically Active Cyclic Phospholipid
Conjugates of Tegafur and Uridine Starting From L-Serine, Synthetic Communications:
An International Journal for Rapid Communication of Synthetic Organic Chemistry,
30:5, 903-909, DOI: 10.1080/00397910008087103
To link to this article: http://dx.doi.org/10.1080/00397910008087103
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