Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Paul R. Parry"'
Publikováno v:
Synthesis. 2003:1035-1038
New shelf-stable pyridylboronic acids have been synthesized: bromine-lithium exchange followed by reaction with triiso-propylborate (TIPB) yielded 2-fluoro-5-pyridylboronic acid (4), 3-bromo-5-pyridylboronic acid (5) and 2-ethoxy-5-pyridylboronic aci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4aa8e970b766b27dabdb56f3cac0fd9e
https://doi.org/10.1055/s-2003-39158
https://doi.org/10.1055/s-2003-39158
Publikováno v:
Organic & Biomolecular Chemistry. 1:1447-1449
5-Formyl-2-furylboronic acid reacts cleanly with a range of heteroaryl bromides under Suzuki–Miyaura cross-coupling conditions to produce 2-formyl-5-heteroarylfuran derivatives. Subsequent Wittig olefination reactions afford π-conjugated alkene–
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::607e114d3ebf1c09eff6df3c639dd3f0
https://doi.org/10.1039/b302767h
https://doi.org/10.1039/b302767h
Autor:
Nezire Saygili, Andrei S. Batsanov, Paul R. Parry, Amy E. Thompson, Brian Tarbit, Martin R. Bryce
Publikováno v:
ChemInform. 36
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0451fffc4bbfed2f2ec6dd93b42afb9b
https://doi.org/10.1002/chin.200538148
https://doi.org/10.1002/chin.200538148
Publikováno v:
ChemInform. 34
5-Formyl-2-furylboronic acid reacts cleanly with a range of heteroaryl bromides under Suzuki–Miyaura cross-coupling conditions to produce 2-formyl-5-heteroarylfuran derivatives. Subsequent Wittig olefination reactions afford π-conjugated alkene–
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9394b2be98f99f377983686e8d85433a
https://doi.org/10.1002/chin.200336088
https://doi.org/10.1002/chin.200336088
Publikováno v:
Organicbiomolecular chemistry. 1(9)
5-Formyl-2-furylboronic acid reacts cleanly with a range of heteroaryl bromides under Suzuki-Miyaura cross-coupling conditions to produce 2-formyl-5-heteroarylfuran derivatives. Subsequent Wittig olefination reactions afford pi-conjugated alkene-pyri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::df1ac2b2dae03a63a79ab074cea49184
https://pubmed.ncbi.nlm.nih.gov/12926269
https://pubmed.ncbi.nlm.nih.gov/12926269
Publikováno v:
The Journal of organic chemistry. 67(21)
2-Bromo-5-pyridylboronic acid 2a, 2-chloro-5-pyridylboronic acid 2b, 2-methoxy-5-pyridylboronic acid 2c, and 5-chloro-2-methoxy-4-pyridylboronic acid 4 have been synthesized and shown to undergo palladium-catalyzed cross-coupling reactions with heter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5c44f5815add9e03c292972882b6c46
https://pubmed.ncbi.nlm.nih.gov/12375993
https://pubmed.ncbi.nlm.nih.gov/12375993
Publikováno v:
ResearcherID
New shelf-stable pyridylboronic acids have been synthesized: bromine-lithium exchange followed by reaction with triiso-propylborate (TIPB) yielded 2-fluoro-5-pyridylboronic acid (4), 3-bromo-5-pyridylboronic acid (5) and 2-ethoxy-5-pyridylboronic aci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42af847a3cfbf7974820f29076672023
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000183084000008&KeyUID=WOS:000183084000008
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000183084000008&KeyUID=WOS:000183084000008
