ChemInform Abstract: Base‐Catalyzed Schmittel Cycloisomerization of o‐Phenylenediyne‐Linked Bis(arenol)s to Indeno[1, 2‐c]chromenes. Issue 17 (28th April 2014)

Record Type:: Journal Article
Title:: ChemInform Abstract: Base‐Catalyzed Schmittel Cycloisomerization of o‐Phenylenediyne‐Linked Bis(arenol)s to Indeno[1, 2‐c]chromenes. Issue 17 (28th April 2014)
Main Title:: ChemInform Abstract: Base‐Catalyzed Schmittel Cycloisomerization of o‐Phenylenediyne‐Linked Bis(arenol)s to Indeno[1, 2‐c]chromenes.
Authors:: Furusawa, Masaki
Arita, Kosuke
Imahori, Tatsushi
Igawa, Kazunobu
Tomooka, Katsuhiko
Irie, Ryo
Abstract:: <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>The present cycloisomerization of (I) to (II) proceeds under transition metal‐free basic conditions involving a domino sequence of the prototropic rearrangement into a putative vinylidene o‐quinone methide intermediate and subsequent formal inverse‐electron‐demand hetero Diels—Alder cycloaddition.</p> </abstract>
Is Part Of:: ChemInform. Volume 45:Issue 17(2014)
Journal:: ChemInform
Issue:: Volume 45:Issue 17(2014)
Issue Display:: Volume 45, Issue 17 (2014)
Year:: 2014
Volume:: 45
Issue:: 17
Issue Sort Value:: 2014-0045-0017-0000
Page Start:: no
Page End:: no
Publication Date:: 2014-04-28
Subjects:: Chemistry -- Abstracts -- Periodicals
540.5
Journal URLs:: http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1522-2667 ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1002/chin.201417151 ↗
Languages:: English
ISSNs:: 0931-7597
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 3158.195000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store
Ingest File:: 3245.xml