Ph<inf>3</inf>P/I<inf>2</inf>-Mediated Synthesis of 3-Aryl-Substituted and 3,4-Disubstituted Coumarins

© Georg Thieme Verlag Stuttgart New York. Ph 3 P/I 2 -Et 3 N-mediated one-pot two-step esterification-cyclization toward 3-aryl coumarins and 3-aryl-4-methylcoumarins is reported. The reaction of a variety of aryl acetic acids containing steric or reactive group with 2-hydroxybenzaldehydes or 2′-hyd...

Full description

Saved in:
Bibliographic Details
Main Authors: Phakhodee W., Duangkamol C., Yamano D., Pattarawarapan M.
Format: Journal
Published: 2017
Online Access:https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85011632872&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/40542
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Chiang Mai University
id th-cmuir.6653943832-40542
record_format dspace
spelling th-cmuir.6653943832-405422017-09-28T04:10:08Z Ph<inf>3</inf>P/I<inf>2</inf>-Mediated Synthesis of 3-Aryl-Substituted and 3,4-Disubstituted Coumarins Phakhodee W. Duangkamol C. Yamano D. Pattarawarapan M. © Georg Thieme Verlag Stuttgart New York. Ph 3 P/I 2 -Et 3 N-mediated one-pot two-step esterification-cyclization toward 3-aryl coumarins and 3-aryl-4-methylcoumarins is reported. The reaction of a variety of aryl acetic acids containing steric or reactive group with 2-hydroxybenzaldehydes or 2′-hydroxyacetophenone proceeded smoothly at room temperature to afford the corresponding products in good to excellent yields using inexpensive and readily available reactants and reagents. 2017-09-28T04:10:08Z 2017-09-28T04:10:08Z 7 Journal 09365214 2-s2.0-85011632872 10.1055/s-0036-1588941 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85011632872&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/40542
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
description © Georg Thieme Verlag Stuttgart New York. Ph 3 P/I 2 -Et 3 N-mediated one-pot two-step esterification-cyclization toward 3-aryl coumarins and 3-aryl-4-methylcoumarins is reported. The reaction of a variety of aryl acetic acids containing steric or reactive group with 2-hydroxybenzaldehydes or 2′-hydroxyacetophenone proceeded smoothly at room temperature to afford the corresponding products in good to excellent yields using inexpensive and readily available reactants and reagents.
format Journal
author Phakhodee W.
Duangkamol C.
Yamano D.
Pattarawarapan M.
spellingShingle Phakhodee W.
Duangkamol C.
Yamano D.
Pattarawarapan M.
Ph<inf>3</inf>P/I<inf>2</inf>-Mediated Synthesis of 3-Aryl-Substituted and 3,4-Disubstituted Coumarins
author_facet Phakhodee W.
Duangkamol C.
Yamano D.
Pattarawarapan M.
author_sort Phakhodee W.
title Ph<inf>3</inf>P/I<inf>2</inf>-Mediated Synthesis of 3-Aryl-Substituted and 3,4-Disubstituted Coumarins
title_short Ph<inf>3</inf>P/I<inf>2</inf>-Mediated Synthesis of 3-Aryl-Substituted and 3,4-Disubstituted Coumarins
title_full Ph<inf>3</inf>P/I<inf>2</inf>-Mediated Synthesis of 3-Aryl-Substituted and 3,4-Disubstituted Coumarins
title_fullStr Ph<inf>3</inf>P/I<inf>2</inf>-Mediated Synthesis of 3-Aryl-Substituted and 3,4-Disubstituted Coumarins
title_full_unstemmed Ph<inf>3</inf>P/I<inf>2</inf>-Mediated Synthesis of 3-Aryl-Substituted and 3,4-Disubstituted Coumarins
title_sort ph<inf>3</inf>p/i<inf>2</inf>-mediated synthesis of 3-aryl-substituted and 3,4-disubstituted coumarins
publishDate 2017
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85011632872&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/40542
_version_ 1681421836872581120