Synthesis of dolichyl phosphate derivatives with fluorescent label at the ω-end of the chain, new tools to study protein glycosylation
- 1 January 2000
- journal article
- research article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 10 (2) , 189-192
- https://doi.org/10.1016/s0960-894x(99)00662-9
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- A simple method for preparing racemic dolichols from the polyprenols of pine needles (Pinus silvestris)Russian Chemical Bulletin, 1999
- Novel cascade of seven radical-mediated 6-endo-trig cyclisations leading to a unique all-trans, anti heptacycleJournal of the Chemical Society, Perkin Transactions 1, 1999
- The Importance of Being DolicholBiochemical and Biophysical Research Communications, 1998
- Reductive Amination of Aldehydes and Ketones with Sodium Triacetoxyborohydride. Studies on Direct and Indirect Reductive Amination Procedures1The Journal of Organic Chemistry, 1996
- New methods of synthesis of linear functionalised (Z)-isoprenoids and their 2,3-dihydro-derivativesRussian Chemical Reviews, 1994
- Polyprenyl phosphates: synthesis and structure-activity relationship for a biosynthetic system of Salmonella anatum O-specific polysaccharideChemistry and Physics of Lipids, 1989
- Long-chain polyprenols in the family pinaceaePhytochemistry, 1984
- Synthesis of optically active forms of (Z)-14-methylhexadec-8-enalTetrahedron, 1978
- Positional selectivity during controlled oxidation of polyolefinsTetrahedron Letters, 1967
- The selective oxidation of the terminal double bonds in squaleneTetrahedron Letters, 1962