Synthesis of carbohydrate conjugates. Chemical modification of monosaccharides via 2,4,6-trichloro-1,3,5-triazine
β Scribed by Michael J. Adam; Laurance D. Hall
- Publisher
- Elsevier Science
- Year
- 1985
- Tongue
- English
- Weight
- 620 KB
- Volume
- 144
- Category
- Article
- ISSN
- 0008-6215
No coin nor oath required. For personal study only.
β¦ Synopsis
Several monosaccharides and organic residues, including alkyl, spin-label and organometallic groups, have been linked in various combinations through nitrogen, oxygen, or sulfur atoms by treatment with 2,4,6-trichloro-1,3,5triazine. *For a preliminary communication, see ref. 1.
π SIMILAR VOLUMES
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
## Abstract (__Ξ±__βAminoalkyl)phosphonates have efficiently been synthesized by multicomponent reaction of aldehydes, amines, and triethyl phosphite in the presence of 2,4,6βtrichloroβ1,3,5βtriazine at room temperature. The products are formed in high yields (83β91%) within 0.5β1β h.
## Abstract For Abstract see ChemInform Abstract in Full Text.