Loading…
Chemoenzymatic formal synthesis of (+)-brazilin
Herein, the manuscript presents a chemoenzymatic formal synthetic route of (+)-brazilin, a homoisoflavonoid natural product with a chroman skeleton cis-fused with a 2,3-dihydro-1 -indene unit, which is isolated from the traditional Chinese medicine, . The key feature of the synthetic strategy includ...
Saved in:
Published in: | Natural product research 2024-05, p.1-11 |
---|---|
Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | cdi_FETCH-LOGICAL-c257t-2e872badcb6873c0eebe19a436e553d0e446a11b5709a76cc9380f2330dcdea13 |
container_end_page | 11 |
container_issue | |
container_start_page | 1 |
container_title | Natural product research |
container_volume | |
creator | Liu, Jiangtao Han, Xue Yu, Liuping Zhang, Jiandong Huang, Shuangping Yang, Xihua Chang, Honghong |
description | Herein, the manuscript presents a chemoenzymatic formal synthetic route of (+)-brazilin, a homoisoflavonoid natural product with a chroman skeleton cis-fused with a 2,3-dihydro-1
-indene unit, which is isolated from the traditional Chinese medicine,
. The key feature of the synthetic strategy includes an enzyme-mediated desymmetrization by employing lipase from
type B (CALB) and a one-pot S
2/hydrolysis reaction. |
doi_str_mv | 10.1080/14786419.2024.2349255 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3051940604</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3051940604</sourcerecordid><originalsourceid>FETCH-LOGICAL-c257t-2e872badcb6873c0eebe19a436e553d0e446a11b5709a76cc9380f2330dcdea13</originalsourceid><addsrcrecordid>eNo9kMtKw0AUhgdRbK0-gpJlRdKeuWeWUrxBwY2uh8nkhEZyqTPpIn36tvSyOj-H_wIfIY8UZhQymFOhMyWomTFgYsa4MEzKKzI-_FMlmL6-aGpG5C7GPwBGpZS3ZMQzTZkUZkzmixU2HbbboXF95ZOyC42rkzi0_QpjFZOuTKYvz2ke3Laqq_ae3JSujvhwuhPy-_72s_hMl98fX4vXZeqZ1H3KMNMsd4XPVaa5B8QcqXGCK5SSF4BCKEdpLjUYp5X3hmdQMs6h8AU6yidkeuxdh-5_g7G3TRU91rVrsdtEy0FSI0CB2Fvl0epDF2PA0q5D1bgwWAr2wMqeWdkDK3titc89nSY2eYPFJXWGw3ebG2MY</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3051940604</pqid></control><display><type>article</type><title>Chemoenzymatic formal synthesis of (+)-brazilin</title><source>Taylor and Francis Science and Technology Collection</source><creator>Liu, Jiangtao ; Han, Xue ; Yu, Liuping ; Zhang, Jiandong ; Huang, Shuangping ; Yang, Xihua ; Chang, Honghong</creator><creatorcontrib>Liu, Jiangtao ; Han, Xue ; Yu, Liuping ; Zhang, Jiandong ; Huang, Shuangping ; Yang, Xihua ; Chang, Honghong</creatorcontrib><description>Herein, the manuscript presents a chemoenzymatic formal synthetic route of (+)-brazilin, a homoisoflavonoid natural product with a chroman skeleton cis-fused with a 2,3-dihydro-1
-indene unit, which is isolated from the traditional Chinese medicine,
. The key feature of the synthetic strategy includes an enzyme-mediated desymmetrization by employing lipase from
type B (CALB) and a one-pot S
2/hydrolysis reaction.</description><identifier>ISSN: 1478-6419</identifier><identifier>EISSN: 1478-6427</identifier><identifier>DOI: 10.1080/14786419.2024.2349255</identifier><identifier>PMID: 38712549</identifier><language>eng</language><publisher>England</publisher><ispartof>Natural product research, 2024-05, p.1-11</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c257t-2e872badcb6873c0eebe19a436e553d0e446a11b5709a76cc9380f2330dcdea13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38712549$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Jiangtao</creatorcontrib><creatorcontrib>Han, Xue</creatorcontrib><creatorcontrib>Yu, Liuping</creatorcontrib><creatorcontrib>Zhang, Jiandong</creatorcontrib><creatorcontrib>Huang, Shuangping</creatorcontrib><creatorcontrib>Yang, Xihua</creatorcontrib><creatorcontrib>Chang, Honghong</creatorcontrib><title>Chemoenzymatic formal synthesis of (+)-brazilin</title><title>Natural product research</title><addtitle>Nat Prod Res</addtitle><description>Herein, the manuscript presents a chemoenzymatic formal synthetic route of (+)-brazilin, a homoisoflavonoid natural product with a chroman skeleton cis-fused with a 2,3-dihydro-1
-indene unit, which is isolated from the traditional Chinese medicine,
. The key feature of the synthetic strategy includes an enzyme-mediated desymmetrization by employing lipase from
type B (CALB) and a one-pot S
2/hydrolysis reaction.</description><issn>1478-6419</issn><issn>1478-6427</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNo9kMtKw0AUhgdRbK0-gpJlRdKeuWeWUrxBwY2uh8nkhEZyqTPpIn36tvSyOj-H_wIfIY8UZhQymFOhMyWomTFgYsa4MEzKKzI-_FMlmL6-aGpG5C7GPwBGpZS3ZMQzTZkUZkzmixU2HbbboXF95ZOyC42rkzi0_QpjFZOuTKYvz2ke3Laqq_ae3JSujvhwuhPy-_72s_hMl98fX4vXZeqZ1H3KMNMsd4XPVaa5B8QcqXGCK5SSF4BCKEdpLjUYp5X3hmdQMs6h8AU6yidkeuxdh-5_g7G3TRU91rVrsdtEy0FSI0CB2Fvl0epDF2PA0q5D1bgwWAr2wMqeWdkDK3titc89nSY2eYPFJXWGw3ebG2MY</recordid><startdate>20240507</startdate><enddate>20240507</enddate><creator>Liu, Jiangtao</creator><creator>Han, Xue</creator><creator>Yu, Liuping</creator><creator>Zhang, Jiandong</creator><creator>Huang, Shuangping</creator><creator>Yang, Xihua</creator><creator>Chang, Honghong</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20240507</creationdate><title>Chemoenzymatic formal synthesis of (+)-brazilin</title><author>Liu, Jiangtao ; Han, Xue ; Yu, Liuping ; Zhang, Jiandong ; Huang, Shuangping ; Yang, Xihua ; Chang, Honghong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c257t-2e872badcb6873c0eebe19a436e553d0e446a11b5709a76cc9380f2330dcdea13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Jiangtao</creatorcontrib><creatorcontrib>Han, Xue</creatorcontrib><creatorcontrib>Yu, Liuping</creatorcontrib><creatorcontrib>Zhang, Jiandong</creatorcontrib><creatorcontrib>Huang, Shuangping</creatorcontrib><creatorcontrib>Yang, Xihua</creatorcontrib><creatorcontrib>Chang, Honghong</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Natural product research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Jiangtao</au><au>Han, Xue</au><au>Yu, Liuping</au><au>Zhang, Jiandong</au><au>Huang, Shuangping</au><au>Yang, Xihua</au><au>Chang, Honghong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chemoenzymatic formal synthesis of (+)-brazilin</atitle><jtitle>Natural product research</jtitle><addtitle>Nat Prod Res</addtitle><date>2024-05-07</date><risdate>2024</risdate><spage>1</spage><epage>11</epage><pages>1-11</pages><issn>1478-6419</issn><eissn>1478-6427</eissn><abstract>Herein, the manuscript presents a chemoenzymatic formal synthetic route of (+)-brazilin, a homoisoflavonoid natural product with a chroman skeleton cis-fused with a 2,3-dihydro-1
-indene unit, which is isolated from the traditional Chinese medicine,
. The key feature of the synthetic strategy includes an enzyme-mediated desymmetrization by employing lipase from
type B (CALB) and a one-pot S
2/hydrolysis reaction.</abstract><cop>England</cop><pmid>38712549</pmid><doi>10.1080/14786419.2024.2349255</doi><tpages>11</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1478-6419 |
ispartof | Natural product research, 2024-05, p.1-11 |
issn | 1478-6419 1478-6427 |
language | eng |
recordid | cdi_proquest_miscellaneous_3051940604 |
source | Taylor and Francis Science and Technology Collection |
title | Chemoenzymatic formal synthesis of (+)-brazilin |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T15%3A55%3A04IST&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=Chemoenzymatic%20formal%20synthesis%20of%20(+)-brazilin&rft.jtitle=Natural%20product%20research&rft.au=Liu,%20Jiangtao&rft.date=2024-05-07&rft.spage=1&rft.epage=11&rft.pages=1-11&rft.issn=1478-6419&rft.eissn=1478-6427&rft_id=info:doi/10.1080/14786419.2024.2349255&rft_dat=%3Cproquest_cross%3E3051940604%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c257t-2e872badcb6873c0eebe19a436e553d0e446a11b5709a76cc9380f2330dcdea13%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=3051940604&rft_id=info:pmid/38712549&rfr_iscdi=true |