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An Efficient Synthesis of Novel Carbocyclic Nucleosides with Use of Ring-Closing Metathesis from d -Lactose

✍ Scribed by Hong, Joon Hee; Shim, Myung Jung; Ro, Bong Oh; Ko, Ok Hyun


Book ID
125995372
Publisher
American Chemical Society
Year
2002
Tongue
English
Weight
82 KB
Volume
67
Category
Article
ISSN
0022-3263

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Efficient synthesis of novel carbocyclic
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Very efficient synthetic route to novel 4%a-C-hydroxymethyl branched carbocyclic nucleosides was described. The stereocontrolled synthesis of target nucleosides was successfully achieved by Johnson orthoester-Claisen rearrangement, ring-closing metathesis (RCM) starting from a simple acyclic precurs

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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a β€œFull Text” option. The original article is trackable v