Issue 4, 1993

Stereoselective C-3 substitution of 1,5-anhydro-2-deoxy-2-formyl-3,4,6-tri-O-methylhex-1-enitols: entry to ribo and xylo series

Abstract

Reaction of 1,5-anhydro-2-deoxy-2-formyl-3,4,6-tri-O-methyl-D-lyxo-hex-1-enitol 1 and its arabino epimer 3 with various nucleophiles under Lewis acid catalysis led to stereoselective C-3 substitution.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1993, 393-394

Stereoselective C-3 substitution of 1,5-anhydro-2-deoxy-2-formyl-3,4,6-tri-O-methylhex-1-enitols: entry to ribo and xylo series

C. Booma and K. K. Balasubramanian, J. Chem. Soc., Perkin Trans. 1, 1993, 393 DOI: 10.1039/P19930000393

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements