Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3122
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
Cleavage of lignin ether bonds transfer hydrogenolysis is a promising route to valorize lignin, thus processes that use mild reaction conditions and exploit renewable hydrogen donor solvents (rather than molecular hydrogen) are economically advantageous. Herein we demonstrate the efficient catalytic transfer hydrogenolysis and tandem decarbonylation of lignin model compounds possessing aromatic ether bonds (α-O-4, β-O-4 and 4-O-5 linkages), over transition metal-modified Pd hydrotalcite catalysts with ethanol as the hydrogen donor and solvent. Quantitative conversions and yields were attained for all model compounds, except for 4-O-5 models, which possess inherently strong sp C-O bonds. The latter demonstrates the utility of Pd hydrotalcite catalysts for transfer hydrogenolysis of model compounds. This process was employed to achieve whole pine biomass delignification with 97% yield and a 22% phenolic monomer yield, with 64% selectivity for 4-(3-hydroxypropyl)-2-methoxyphenol.
Download full-text PDF |
Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11587535 | PMC |
http://dx.doi.org/10.1039/d4sc03942d | DOI Listing |
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