We herein report simple and efficient methods for the synthesis of various formyl derivatives of dibenzofuran. The aldehydes reported are prepared in at most three steps and in yields greater than 60% from commercially available dibenzofuran, with one exception where isomers must be separated. The protocols described involve either formylation of previously functionalized dibenzofuran derivatives or the initial introduction of the formyl group and subsequent further functionalization under standard reaction conditions as described. We have also reported an efficient and simple method for the synthesis of keywords methoxydibenzofurans in high yield (65% overall for two steps
%0 Journal Article
%1 RN292
%A Yempala, T.
%A Cassels, B.K.
%D 2016
%J Synthetic Communications
%K acid antitubercular arylation, bond bromo carbaldehydes, cascade, derivatives, design, dibenzofuran dqcauchile efficient evaluation, formation, formylation, furans, methoxy phytoalexins, protocols, stems,
%N 23
%P 1909-1915
%R 10.1080/00397911.2016.1235201
%T Simple and Efficient Synthesis of Various Dibenzofuran Carbaldehydes
%U /brokenurl#<Go to ISI>://WOS:000388722500006
%V 46
%X We herein report simple and efficient methods for the synthesis of various formyl derivatives of dibenzofuran. The aldehydes reported are prepared in at most three steps and in yields greater than 60% from commercially available dibenzofuran, with one exception where isomers must be separated. The protocols described involve either formylation of previously functionalized dibenzofuran derivatives or the initial introduction of the formyl group and subsequent further functionalization under standard reaction conditions as described. We have also reported an efficient and simple method for the synthesis of keywords methoxydibenzofurans in high yield (65% overall for two steps
@article{RN292,
abstract = {We herein report simple and efficient methods for the synthesis of various formyl derivatives of dibenzofuran. The aldehydes reported are prepared in at most three steps and in yields greater than 60% from commercially available dibenzofuran, with one exception where isomers must be separated. The protocols described involve either formylation of previously functionalized dibenzofuran derivatives or the initial introduction of the formyl group and subsequent further functionalization under standard reaction conditions as described. We have also reported an efficient and simple method for the synthesis of keywords methoxydibenzofurans in high yield (65% overall for two steps},
added-at = {2019-12-04T03:57:35.000+0100},
author = {Yempala, T. and Cassels, B.K.},
biburl = {https://www.bibsonomy.org/bibtex/281d07051c2c8a1710b173b9fac4e10b7/dqcauchile},
doi = {10.1080/00397911.2016.1235201},
interhash = {de5a1557350d0bc2819ba701868bbdb9},
intrahash = {81d07051c2c8a1710b173b9fac4e10b7},
issn = {0039-7911},
journal = {Synthetic Communications},
keywords = {acid antitubercular arylation, bond bromo carbaldehydes, cascade, derivatives, design, dibenzofuran dqcauchile efficient evaluation, formation, formylation, furans, methoxy phytoalexins, protocols, stems,},
number = 23,
pages = {1909-1915},
timestamp = {2019-12-04T03:58:17.000+0100},
title = {Simple and Efficient Synthesis of Various Dibenzofuran Carbaldehydes},
type = {Journal Article},
url = {/brokenurl#<Go to ISI>://WOS:000388722500006},
volume = 46,
year = 2016
}