Abstract
Asymmetric synthesis of 1,4-dideoxy-1,4-imino-D-ribitol was achieved utilizing the stereoselective addition of allylphenylsulfone to a chiral N-sulfinyl-2-furfuryl imine and ring-closing metathesis reactions as key steps.
Original language | English |
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Pages (from-to) | 3409-3415 |
Number of pages | 7 |
Journal | Tetrahedron Asymmetry |
Volume | 12 |
Issue number | 24 |
DOIs | |
State | Published - 21 Jan 2002 |
Bibliographical note
Funding Information:Support of this research by a grant from the US–Israel Binational Science Foundation and from the Marcus Center for Medicinal and Pharmaceutical Chemistry is gratefully acknowledged. We thank Dr. H. E. Gottlieb for valuable help with NMR spectra.
Funding
Support of this research by a grant from the US–Israel Binational Science Foundation and from the Marcus Center for Medicinal and Pharmaceutical Chemistry is gratefully acknowledged. We thank Dr. H. E. Gottlieb for valuable help with NMR spectra.
Funders | Funder number |
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US-Israel Binational Science Foundation |