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Article: Stereoregular Oligomerization by Repetitive Diels–Alder Reactions

TitleStereoregular Oligomerization by Repetitive Diels–Alder Reactions
Authors
Ashton, Peter R.Isaacs, Neil S.Kohnke, Franz H.Mathias, John P.Stoddart, J. Fraser
Issue Date1989
Citation
Angewandte Chemie International Edition in English, 1989, v. 28, n. 9, p. 1258-1261 How to Cite?
DOI: http://dx.doi.org/10.1002/anie.198912581
AbstractHighly stereoselective preparation of the oligomer 1 is possible “simply” by means of a structure‐directed synthesis, that is, without any use of controlling reagents or catalysts. The 3 :2 Diets–Alder adduct of diene and dienophile has an all‐syn configuration and is coiled in such a way that the two ends approach each other. (Figure Presented.) Copyright © 1989 by VCH Verlagsgesellschaft mbH, Germany
Persistent Identifierhttp://hdl.handle.net/10722/333226
ISSN
0570-0833
ISI Accession Number ID
WOS:A1989AU08000029

 

DC FieldValueLanguage
dc.contributor.authorAshton, Peter R.-
dc.contributor.authorIsaacs, Neil S.-
dc.contributor.authorKohnke, Franz H.-
dc.contributor.authorMathias, John P.-
dc.contributor.authorStoddart, J. Fraser-
dc.date.accessioned2023-10-06T05:17:40Z-
dc.date.available2023-10-06T05:17:40Z-
dc.date.issued1989-
dc.identifier.citationAngewandte Chemie International Edition in English, 1989, v. 28, n. 9, p. 1258-1261-
dc.identifier.issn0570-0833-
dc.identifier.urihttp://hdl.handle.net/10722/333226-
dc.description.abstractHighly stereoselective preparation of the oligomer 1 is possible “simply” by means of a structure‐directed synthesis, that is, without any use of controlling reagents or catalysts. The 3 :2 Diets–Alder adduct of diene and dienophile has an all‐syn configuration and is coiled in such a way that the two ends approach each other. (Figure Presented.) Copyright © 1989 by VCH Verlagsgesellschaft mbH, Germany-
dc.languageeng-
dc.relation.ispartofAngewandte Chemie International Edition in English-
dc.titleStereoregular Oligomerization by Repetitive Diels–Alder Reactions-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1002/anie.198912581-
dc.identifier.scopuseid_2-s2.0-84990113704-
dc.identifier.volume28-
dc.identifier.issue9-
dc.identifier.spage1258-
dc.identifier.epage1261-
dc.identifier.eissn1521-3773-
dc.identifier.isiWOS:A1989AU08000029-

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