12895080

Source:http://linkedlifedata.com/resource/pubmed/id/12895080

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0001975, umls-concept:C0048721, umls-concept:C0063796, umls-concept:C0205314, umls-concept:C0311404, umls-concept:C0439851, umls-concept:C0679622, umls-concept:C1521827, umls-concept:C1552596, umls-concept:C1883254, umls-concept:C1947931
pubmed:issue	16
pubmed:dateCreated	2003-8-4
pubmed:abstractText	alpha-Tosyloxyketones and alpha-tosyloxyaldehydes were directly prepared from alcohols by treatment with iodosylbenzene and p-toluenesulfonic acid monohydrate in good yields. This method can be used for the direct preparation of thiazoles, imidazoles, and imidazo[1,2-a]pyridines from alcohols in good to moderate yields by the successive treatment with iodosylbenzene and p-toluenesulfonic acid monohydrate, followed by thioamides, benzamidine, and 2-aminopyridine, respectively.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985193R
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Aug
pubmed:issn	0022-3263
pubmed:author	pubmed-author:NabanaTakahiroT, pubmed-author:TogoHideoH, pubmed-author:UenoMakotoM
pubmed:issnType	Print
pubmed:day	8
pubmed:volume	68
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	6424-6
pubmed:year	2003
pubmed:articleTitle	Novel oxidative alpha-tosyloxylation of alcohols with iodosylbenzene and p-toluenesulfonic acid and its synthetic use for direct preparation of heteroaromatics.
pubmed:affiliation	Graduate School of Science and Technology, and Department of Chemistry, Faculty of Science, Chiba University, Yayoi-cho 1-33, Inage-ku, Chiba 263-8522 Japan.
pubmed:publicationType	Journal Article