Loading…

Three New Chromanones from Calea clausseniana

Three new chromanones, uniflorol A acetate (1), uniflorol B acetate (2), and 2,2‐dimethyl‐6‐{1‐[(4′‐acetoxy)angeloyloxy]ethyl}chroman‐4‐one (3), together with the known chromanone 4, and two known p‐hydroxyacetophenone derivatives, 5 and 6, were isolated from the CH2Cl2 crude extract of the undergro...

Full description

Saved in:
Bibliographic Details
Published in:Helvetica chimica acta 2014-01, Vol.97 (1), p.146-150
Main Authors: doNascimento, Andréa M, deOliveira, Dionéia C R
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c3557-d711b42a14fb21095a067a7456c6df70a313661ed488c0ca79059965ece258c33
cites cdi_FETCH-LOGICAL-c3557-d711b42a14fb21095a067a7456c6df70a313661ed488c0ca79059965ece258c33
container_end_page 150
container_issue 1
container_start_page 146
container_title Helvetica chimica acta
container_volume 97
creator doNascimento, Andréa M
deOliveira, Dionéia C R
description Three new chromanones, uniflorol A acetate (1), uniflorol B acetate (2), and 2,2‐dimethyl‐6‐{1‐[(4′‐acetoxy)angeloyloxy]ethyl}chroman‐4‐one (3), together with the known chromanone 4, and two known p‐hydroxyacetophenone derivatives, 5 and 6, were isolated from the CH2Cl2 crude extract of the underground parts of Calea clausseniana Baker. The structures of the new compounds were elucidated by spectroscopic analyses, including 2D‐NMR techniques.
doi_str_mv 10.1002/hlca.201300277
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_1477931175</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3183825641</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3557-d711b42a14fb21095a067a7456c6df70a313661ed488c0ca79059965ece258c33</originalsourceid><addsrcrecordid>eNqFkE1PAjEQhhujiYhePW_ieXGm3bbbI9kIGAE94MetKaUbFpddbCHIv3fJGuLN07yTPM9M8hJyi9BDAHq_LK3pUUDWLFKekQ5ySmMqJD8nHQBMY0D1cUmuQlgBgFIgOySeLb1z0dTto2zp67Wp6sqFKG9ilJnSmciWZheCqwpTmWtykZsyuJvf2SWvg4dZNorHz8PHrD-OLeNcxguJOE-owSSfUwTFDQhpZMKFFYtcgmHIhEC3SNLUgjVSAVdKcGcd5allrEvu2rsbX3_tXNjqVb3zVfNSYyKlYoiSN1SvpayvQ_Au1xtfrI0_aAR9rEQfK9GnShpBtcK-KN3hH1qPxln_rxu3bhG27vvkGv-phWSS6_fpUL-o4eRpMnjTnP0A6n5x3Q</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1477931175</pqid></control><display><type>article</type><title>Three New Chromanones from Calea clausseniana</title><source>Wiley</source><creator>doNascimento, Andréa M ; deOliveira, Dionéia C R</creator><creatorcontrib>doNascimento, Andréa M ; deOliveira, Dionéia C R</creatorcontrib><description>Three new chromanones, uniflorol A acetate (1), uniflorol B acetate (2), and 2,2‐dimethyl‐6‐{1‐[(4′‐acetoxy)angeloyloxy]ethyl}chroman‐4‐one (3), together with the known chromanone 4, and two known p‐hydroxyacetophenone derivatives, 5 and 6, were isolated from the CH2Cl2 crude extract of the underground parts of Calea clausseniana Baker. The structures of the new compounds were elucidated by spectroscopic analyses, including 2D‐NMR techniques.</description><identifier>ISSN: 0018-019X</identifier><identifier>EISSN: 1522-2675</identifier><identifier>DOI: 10.1002/hlca.201300277</identifier><language>eng</language><publisher>Zürich: WILEY-VCH Verlag</publisher><subject>Acetophenones ; Acetophenones, p‐hydroxy ; Calea clausseniana ; Chromanones ; p-hydroxy ; Vegetables</subject><ispartof>Helvetica chimica acta, 2014-01, Vol.97 (1), p.146-150</ispartof><rights>Copyright © 2014 Verlag Helvetica Chimica Acta AG, Zürich</rights><rights>Copyright © 2014 Verlag Helvetica Chimica Acta AG, Zurich</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3557-d711b42a14fb21095a067a7456c6df70a313661ed488c0ca79059965ece258c33</citedby><cites>FETCH-LOGICAL-c3557-d711b42a14fb21095a067a7456c6df70a313661ed488c0ca79059965ece258c33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>doNascimento, Andréa M</creatorcontrib><creatorcontrib>deOliveira, Dionéia C R</creatorcontrib><title>Three New Chromanones from Calea clausseniana</title><title>Helvetica chimica acta</title><addtitle>HCA</addtitle><description>Three new chromanones, uniflorol A acetate (1), uniflorol B acetate (2), and 2,2‐dimethyl‐6‐{1‐[(4′‐acetoxy)angeloyloxy]ethyl}chroman‐4‐one (3), together with the known chromanone 4, and two known p‐hydroxyacetophenone derivatives, 5 and 6, were isolated from the CH2Cl2 crude extract of the underground parts of Calea clausseniana Baker. The structures of the new compounds were elucidated by spectroscopic analyses, including 2D‐NMR techniques.</description><subject>Acetophenones</subject><subject>Acetophenones, p‐hydroxy</subject><subject>Calea clausseniana</subject><subject>Chromanones</subject><subject>p-hydroxy</subject><subject>Vegetables</subject><issn>0018-019X</issn><issn>1522-2675</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqFkE1PAjEQhhujiYhePW_ieXGm3bbbI9kIGAE94MetKaUbFpddbCHIv3fJGuLN07yTPM9M8hJyi9BDAHq_LK3pUUDWLFKekQ5ySmMqJD8nHQBMY0D1cUmuQlgBgFIgOySeLb1z0dTto2zp67Wp6sqFKG9ilJnSmciWZheCqwpTmWtykZsyuJvf2SWvg4dZNorHz8PHrD-OLeNcxguJOE-owSSfUwTFDQhpZMKFFYtcgmHIhEC3SNLUgjVSAVdKcGcd5allrEvu2rsbX3_tXNjqVb3zVfNSYyKlYoiSN1SvpayvQ_Au1xtfrI0_aAR9rEQfK9GnShpBtcK-KN3hH1qPxln_rxu3bhG27vvkGv-phWSS6_fpUL-o4eRpMnjTnP0A6n5x3Q</recordid><startdate>201401</startdate><enddate>201401</enddate><creator>doNascimento, Andréa M</creator><creator>deOliveira, Dionéia C R</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope></search><sort><creationdate>201401</creationdate><title>Three New Chromanones from Calea clausseniana</title><author>doNascimento, Andréa M ; deOliveira, Dionéia C R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3557-d711b42a14fb21095a067a7456c6df70a313661ed488c0ca79059965ece258c33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Acetophenones</topic><topic>Acetophenones, p‐hydroxy</topic><topic>Calea clausseniana</topic><topic>Chromanones</topic><topic>p-hydroxy</topic><topic>Vegetables</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>doNascimento, Andréa M</creatorcontrib><creatorcontrib>deOliveira, Dionéia C R</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Helvetica chimica acta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>doNascimento, Andréa M</au><au>deOliveira, Dionéia C R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Three New Chromanones from Calea clausseniana</atitle><jtitle>Helvetica chimica acta</jtitle><addtitle>HCA</addtitle><date>2014-01</date><risdate>2014</risdate><volume>97</volume><issue>1</issue><spage>146</spage><epage>150</epage><pages>146-150</pages><issn>0018-019X</issn><eissn>1522-2675</eissn><abstract>Three new chromanones, uniflorol A acetate (1), uniflorol B acetate (2), and 2,2‐dimethyl‐6‐{1‐[(4′‐acetoxy)angeloyloxy]ethyl}chroman‐4‐one (3), together with the known chromanone 4, and two known p‐hydroxyacetophenone derivatives, 5 and 6, were isolated from the CH2Cl2 crude extract of the underground parts of Calea clausseniana Baker. The structures of the new compounds were elucidated by spectroscopic analyses, including 2D‐NMR techniques.</abstract><cop>Zürich</cop><pub>WILEY-VCH Verlag</pub><doi>10.1002/hlca.201300277</doi><tpages>5</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0018-019X
ispartof Helvetica chimica acta, 2014-01, Vol.97 (1), p.146-150
issn 0018-019X
1522-2675
language eng
recordid cdi_proquest_journals_1477931175
source Wiley
subjects Acetophenones
Acetophenones, p‐hydroxy
Calea clausseniana
Chromanones
p-hydroxy
Vegetables
title Three New Chromanones from Calea clausseniana
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-29T11%3A51%3A42IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Three%20New%20Chromanones%20from%20Calea%20clausseniana&rft.jtitle=Helvetica%20chimica%20acta&rft.au=doNascimento,%20Andr%C3%A9a%20M&rft.date=2014-01&rft.volume=97&rft.issue=1&rft.spage=146&rft.epage=150&rft.pages=146-150&rft.issn=0018-019X&rft.eissn=1522-2675&rft_id=info:doi/10.1002/hlca.201300277&rft_dat=%3Cproquest_cross%3E3183825641%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3557-d711b42a14fb21095a067a7456c6df70a313661ed488c0ca79059965ece258c33%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1477931175&rft_id=info:pmid/&rfr_iscdi=true