17594024

Source:http://linkedlifedata.com/resource/pubmed/id/17594024

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0010546, umls-concept:C0025663, umls-concept:C0038760, umls-concept:C0072780, umls-concept:C0441513, umls-concept:C1260969, umls-concept:C1527177
pubmed:issue	26
pubmed:dateCreated	2007-6-27
pubmed:abstractText	Normally disfavored 5-endo-trig cyclizations proceed in N-homoallylsulfonamides bearing a CF(3), CCl(3), CO(2)Et or CN group at the C-3 position, via an intramolecular S(N)2'-type or addition reaction to construct pyrrolidine rings, even though the system allows a more favorable 5-exo-trig pathway.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9610838
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Jul
pubmed:issn	1359-7345
pubmed:author	pubmed-author:IchikawaJunjiJ, pubmed-author:IwaiYuY, pubmed-author:LapointeGuillaumeG
pubmed:issnType	Print
pubmed:day	14
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	2698-700
pubmed:year	2007
pubmed:articleTitle	Nucleophilic 5-endo-trig cyclizations of N-homoallylic sulfonamides: a facile method for the construction of pyrrolidine rings.
pubmed:affiliation	Department of Chemistry, Graduate School of Science, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo, Japan. junji@chem.s.u-tokyo.ac.jp
pubmed:publicationType	Journal Article