Synthetic Usefulness of the Sugar Cyclopentylidene Ketals
- 1 January 1990
- journal article
- research article
- Published by Taylor & Francis in Journal of Carbohydrate Chemistry
- Vol. 9 (6) , 823-835
- https://doi.org/10.1080/07328309008543877
Abstract
Cyclopentylidene ketals, moderately more acid-labile than their isopropylidene analogs, offer an alternative to the latter blocking groups. They have been shown to resist a large variety of reaction conditions commonly encountered in carbohydrate chemistry.This publication has 4 references indexed in Scilit:
- Terminal Deoxy Hydroxyamino SugarsJournal of Carbohydrate Chemistry, 1988
- Synthèse d'acétals de désoxy-3-hydroxyamino-3-furannoses. Note de laboratoireHelvetica Chimica Acta, 1986
- Oligonucleotidic compounds. V. 2',3'-O-Alkylidene derivatives of ribonucleosidesCollection of Czechoslovak Chemical Communications, 1963
- DERIVATIVES OF MONOACETONE XYLOSEPublished by Elsevier ,1933