Abstract
The 2,4-bis-thinocarbonate 3 of 1,6-anyhydro-D-glucose 1 can be transformed to the corresponding dideoxy compound 5 with diphenylsilane 7 as well as with tris(trimethylsilyl)silane 4 in a radical chain reaction.
| Original language | English |
|---|---|
| Pages (from-to) | 6629-6632 |
| Number of pages | 4 |
| Journal | Tetrahedron Letters |
| Volume | 33 |
| Issue number | 44 |
| DOIs | |
| Publication status | Published - 1992 Oct 27 |
All Science Journal Classification (ASJC) codes
- Biochemistry
- Drug Discovery
- Organic Chemistry
Fingerprint Dive into the research topics of 'Tris(trimethylsilyl)silane and diphenylsilane in the radical chain dideoxygenation of 1,6-anhydro-D-glucose: A comparative study'. Together they form a unique fingerprint.
Cite this
Barton, D. H. R., Doo, O. J., & Jaszberenyi, J. C. (1992). Tris(trimethylsilyl)silane and diphenylsilane in the radical chain dideoxygenation of 1,6-anhydro-D-glucose: A comparative study. Tetrahedron Letters, 33(44), 6629-6632. https://doi.org/10.1016/S0040-4039(00)61003-1