Synthesis and diatropicity of trans-2′,5′,10b,10c-tetramethylfurano[3,4-e]-10b,10c-dihydropyrene. A valence isomerization to form a novel isoannulenofuran at the expense of two benzene and one furan rings

Journal of Organic Chemistry

Saved in:

Bibliographic Details
Main Authors:	Lai, Y.-H., Chen, P.
Other Authors:	CHEMISTRY
Format:	Article
Published:	2014
Online Access:	http://scholarbank.nus.edu.sg/handle/10635/95057
Tags:	Add Tag No Tags, Be the first to tag this record!
Institution:	National University of Singapore

id	sg-nus-scholar.10635-95057
record_format	dspace
spelling	sg-nus-scholar.10635-950572024-11-10T16:58:49Z Synthesis and diatropicity of trans-2′,5′,10b,10c-tetramethylfurano[3,4-e]-10b,10c-dihydropyrene. A valence isomerization to form a novel isoannulenofuran at the expense of two benzene and one furan rings Lai, Y.-H. Chen, P. CHEMISTRY Journal of Organic Chemistry 61 3 935-940 JOCEA 2014-10-16T08:43:19Z 2014-10-16T08:43:19Z 1996-02-09 Article Lai, Y.-H.,Chen, P. (1996-02-09). Synthesis and diatropicity of trans-2′,5′,10b,10c-tetramethylfurano[3,4-e]-10b,10c-dihydropyrene. A valence isomerization to form a novel isoannulenofuran at the expense of two benzene and one furan rings. Journal of Organic Chemistry 61 (3) : 935-940. ScholarBank@NUS Repository. 00223263 http://scholarbank.nus.edu.sg/handle/10635/95057 NOT_IN_WOS Scopus
institution	National University of Singapore
building	NUS Library
continent	Asia
country	Singapore Singapore
content_provider	NUS Library
collection	ScholarBank@NUS
description	Journal of Organic Chemistry
author2	CHEMISTRY
author_facet	CHEMISTRY Lai, Y.-H. Chen, P.
format	Article
author	Lai, Y.-H. Chen, P.
spellingShingle	Lai, Y.-H. Chen, P. Synthesis and diatropicity of trans-2′,5′,10b,10c-tetramethylfurano[3,4-e]-10b,10c-dihydropyrene. A valence isomerization to form a novel isoannulenofuran at the expense of two benzene and one furan rings
author_sort	Lai, Y.-H.
title	Synthesis and diatropicity of trans-2′,5′,10b,10c-tetramethylfurano[3,4-e]-10b,10c-dihydropyrene. A valence isomerization to form a novel isoannulenofuran at the expense of two benzene and one furan rings
title_short	Synthesis and diatropicity of trans-2′,5′,10b,10c-tetramethylfurano[3,4-e]-10b,10c-dihydropyrene. A valence isomerization to form a novel isoannulenofuran at the expense of two benzene and one furan rings
title_full	Synthesis and diatropicity of trans-2′,5′,10b,10c-tetramethylfurano[3,4-e]-10b,10c-dihydropyrene. A valence isomerization to form a novel isoannulenofuran at the expense of two benzene and one furan rings
title_fullStr	Synthesis and diatropicity of trans-2′,5′,10b,10c-tetramethylfurano[3,4-e]-10b,10c-dihydropyrene. A valence isomerization to form a novel isoannulenofuran at the expense of two benzene and one furan rings
title_full_unstemmed	Synthesis and diatropicity of trans-2′,5′,10b,10c-tetramethylfurano[3,4-e]-10b,10c-dihydropyrene. A valence isomerization to form a novel isoannulenofuran at the expense of two benzene and one furan rings
title_sort	synthesis and diatropicity of trans-2′,5′,10b,10c-tetramethylfurano[3,4-e]-10b,10c-dihydropyrene. a valence isomerization to form a novel isoannulenofuran at the expense of two benzene and one furan rings
publishDate	2014
url	http://scholarbank.nus.edu.sg/handle/10635/95057
_version_	1821217902501560320

Synthesis and diatropicity of trans-2′,5′,10b,10c-tetramethylfurano[3,4-e]-10b,10c-dihydropyrene. A valence isomerization to form a novel isoannulenofuran at the expense of two benzene and one furan rings

Similar Items