| dc.contributor.author | Munavu Raphael M | |
| dc.contributor.author | Nasseri-Noori B | |
| dc.contributor.author | Szmant HH | |
| dc.date.accessioned | 2013-05-29T15:03:14Z | |
| dc.date.available | 2013-05-29T15:03:14Z | |
| dc.date.issued | 1984-02 | |
| dc.identifier.citation | Myristoyl Esters of Lactose", Carbohydrate Research, 125, 253-263., M., PROF. MUNAVU RAPHAEL , J. Sci. Technol. (Kenya), 5, 45- 52 (1984)., (1984) copy at http://profiles.uonbi.ac.ke/rmmunavu/publications/myristoyl-esters-lactose-carbohydrate-research-125-253-263 | en |
| dc.identifier.uri | http://profiles.uonbi.ac.ke/rmmunavu/publications/myristoyl-esters-lactose-carbohydrate-research-125-253-263 | |
| dc.identifier.uri | http://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/27173 | |
| dc.identifier.uri | http://www.ncbi.nlm.nih.gov/pubmed/6704996 | |
| dc.description.abstract | Whereas lactose did not undergo a base-catalyzed transesterification with methyl esters of fatty acids, methyl beta-lactoside reacted under identical conditions to give mono- and di-myristates. This difference in behavior is explained in terms of the formation of an unreactive, internally chelated potassium-lactose complex. Supporting evidence for this hypothesis is the observed change in the anomeric equilibrium of lactose in the presence of potassium carbonate. The monomyristates of methyl beta-lactoside were assigned the structures of 3' and 6' derivatives, and it is concluded that the diesters are the 3',6', and 6,6' derivatives. | |
| dc.language.iso | en | en |
| dc.publisher | J. Sci. Technol | en |
| dc.title | Myristoyl Esters of Lactose", Carbohydrate Research, 125, 253-263. | en |
| dc.type | Article | en |
| local.publisher | Department of Chemistry | en |
