This submission belongs to the session a. General Organic Synthesis of the event The 8th International Electronic Conference on Synthetic Organic Chemistry
Published date
01 Nov, 2004
Citation
M. Martinková, M. Šoteková, J. Gonda, M. Budĕšínský, I. Císařová, Contribution to the Stereoselective Synthesis of (3'S)-Isothiocyanato-3'-C-vinyl-3'-deoxyuridine and Its Derivatives, in Proceedings of The 8th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2004, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-8-01954
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Contribution to the Stereoselective Synthesis of (3'S)-Isothiocyanato-3'-C-vinyl-3'-deoxyuridine and Its Derivatives
M. Martinková 1
M. Šoteková 1
J. Gonda 1
M. Budĕšínský 2
I. Císařová 3
1. Department of Organic Chemistry, Institute of Chemical Sciences, P. J. Šafárik University, SK-041 67 Košice, Slovakia
2. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, CZ-166 10 Prague, Czech Republic
3. Department of Inorganic Chemistry, Faculty of Sciences of the Charles University, CZ-128 40 Prague, Czech Republic
Abstract
A stereoselective synthesis of the (3¢S)-isothiocyanato-3¢-C-vinyl-3¢-deoxyuridine via (3,3)-sigmatropic rearrangement of allylic thiocyanate derived from protected uridine was investigated.
Keywords
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