12643315

Source:http://linkedlifedata.com/resource/pubmed/id/12643315

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0025664, umls-concept:C0184511, umls-concept:C0220781, umls-concept:C1883254
pubmed:issue	6
pubmed:dateCreated	2003-3-19
pubmed:abstractText	An improved methodology to prepare (S)2,3-O-cyclohexylideneglyceraldehyde is described. Starting from the commercially available (L)-cyclohexylidene protected ascorbic acid the enantiomerically pure aldehyde was synthesized in only two steps in 41% overall yield.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9612491
pubmed:status	PubMed-not-MEDLINE
pubmed:issn	1024-2430
pubmed:author	pubmed-author:BenagliaMM, pubmed-author:CaporaleMM, pubmed-author:PuglisiAA
pubmed:issnType	Print
pubmed:volume	7
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	383-5
pubmed:dateRevised	2003-11-4
pubmed:articleTitle	An improved methodology for the synthesis of enantiomerically pure (S)-2,3-O-cyclohexylideneglyceraldehyde.
pubmed:affiliation	Dipartimento di Chimica Organica e Industriale, Università degli Studi di Milano, Via Golgi, 19, 20133 Milano, Italy. Maurizio.Benaglia@unimi.it
pubmed:publicationType	Journal Article