7-(1-Acetoxymethylidene)Benzonorbornadiene:  A Versatile Reagent for the Synthesis of 7-Formyl and 7-Hydroxymethyl Benzonorbornadienes

7-(1-Acetoxymethylidene)benzonorbornadiene [Formula: see text] , prepared in one step by the addition of benzyne to 6-acetoxyfulvene [Formula: see text] , is hydrolysed in acid solution to form a 3:2-epimeric mixture of syn- and anti- 7-formylbenzonorbornadienes [Formula: see text] and [Formula: see...

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Detalles Bibliográficos
Autores principales: Warrener, Ronald N., Collin, Geoffrey J., Foley, Patrick J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2001
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6236343/
http://dx.doi.org/10.3390/60300194
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author Warrener, Ronald N.
Collin, Geoffrey J.
Foley, Patrick J.
author_facet Warrener, Ronald N.
Collin, Geoffrey J.
Foley, Patrick J.
author_sort Warrener, Ronald N.
collection PubMed
description 7-(1-Acetoxymethylidene)benzonorbornadiene [Formula: see text] , prepared in one step by the addition of benzyne to 6-acetoxyfulvene [Formula: see text] , is hydrolysed in acid solution to form a 3:2-epimeric mixture of syn- and anti- 7-formylbenzonorbornadienes [Formula: see text] and [Formula: see text] , respectively; the corresponding 7-hydroxymethylbenzonorbornadienes [Formula: see text] and [Formula: see text] were produced by reduction of the formyl isomers with sodium borohydride.
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spelling pubmed-62363432018-11-19 7-(1-Acetoxymethylidene)Benzonorbornadiene:  A Versatile Reagent for the Synthesis of 7-Formyl and 7-Hydroxymethyl Benzonorbornadienes Warrener, Ronald N. Collin, Geoffrey J. Foley, Patrick J. Molecules Article 7-(1-Acetoxymethylidene)benzonorbornadiene [Formula: see text] , prepared in one step by the addition of benzyne to 6-acetoxyfulvene [Formula: see text] , is hydrolysed in acid solution to form a 3:2-epimeric mixture of syn- and anti- 7-formylbenzonorbornadienes [Formula: see text] and [Formula: see text] , respectively; the corresponding 7-hydroxymethylbenzonorbornadienes [Formula: see text] and [Formula: see text] were produced by reduction of the formyl isomers with sodium borohydride. MDPI 2001-02-28 /pmc/articles/PMC6236343/ http://dx.doi.org/10.3390/60300194 Text en © 2001 by MDPI (http://www.mdpi.org). Reproduction is permitted for noncommercial purposes.
spellingShingle Article
Warrener, Ronald N.
Collin, Geoffrey J.
Foley, Patrick J.
7-(1-Acetoxymethylidene)Benzonorbornadiene:  A Versatile Reagent for the Synthesis of 7-Formyl and 7-Hydroxymethyl Benzonorbornadienes
title 7-(1-Acetoxymethylidene)Benzonorbornadiene:  A Versatile Reagent for the Synthesis of 7-Formyl and 7-Hydroxymethyl Benzonorbornadienes
title_full 7-(1-Acetoxymethylidene)Benzonorbornadiene:  A Versatile Reagent for the Synthesis of 7-Formyl and 7-Hydroxymethyl Benzonorbornadienes
title_fullStr 7-(1-Acetoxymethylidene)Benzonorbornadiene:  A Versatile Reagent for the Synthesis of 7-Formyl and 7-Hydroxymethyl Benzonorbornadienes
title_full_unstemmed 7-(1-Acetoxymethylidene)Benzonorbornadiene:  A Versatile Reagent for the Synthesis of 7-Formyl and 7-Hydroxymethyl Benzonorbornadienes
title_short 7-(1-Acetoxymethylidene)Benzonorbornadiene:  A Versatile Reagent for the Synthesis of 7-Formyl and 7-Hydroxymethyl Benzonorbornadienes
title_sort 7-(1-acetoxymethylidene)benzonorbornadiene:  a versatile reagent for the synthesis of 7-formyl and 7-hydroxymethyl benzonorbornadienes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6236343/
http://dx.doi.org/10.3390/60300194
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