Zobrazeno 1 - 10
of 112
pro vyhledávání: '"Eoghan M. McGarrigle"'
Publikováno v:
Organicbiomolecular chemistry.
Thiourea catalysts activated α,β-unsaturated phosphonates and phosphinates toward conjugate addition by amines to give β-aminophosphonates and β-aminophosphinates. The organocatalytic methodology was used to synthesise 15 β-aminophosphonates and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a365cce67a0c3831cb640c98df4554c3
https://pubmed.ncbi.nlm.nih.gov/36607271
https://pubmed.ncbi.nlm.nih.gov/36607271
Publikováno v:
Chemical Communications.
An efficient transition-metal free iodine-mediated tuneable disulfonylation and sulfinylsulfonylation of alkynes with sodium arylsulfinates under visible light irradiation has been developed. This photochemical protocol offers broad substrate scope o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f49569eb941a5139c95b85b4fb85e21
https://doi.org/10.1039/d3cc02011h
https://doi.org/10.1039/d3cc02011h
Publikováno v:
Chemical Science
Stereoselective β-mannosylation is one of the most challenging problems in the synthesis of oligosaccharides. Herein, a highly selective synthesis of β-mannosides and β-rhamnosides from glycosyl hemi-acetals is reported, following a one-pot chlori
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6de67e13d51f7b0fc73d60fd0a6fd860
http://europepmc.org/articles/PMC8317664
http://europepmc.org/articles/PMC8317664
Publikováno v:
ARKIVOC, Vol 2007, Iss 5, Pp 139-151 (2006)
Externí odkaz:
https://doaj.org/article/a67c5048f96d411ab9593ffbd9ec4b43
Publikováno v:
ARKIVOC, Vol 2005, Iss 1, Pp 30-38 (2004)
Externí odkaz:
https://doaj.org/article/973584b2264d4427b4f38850c6bc0cab
Publikováno v:
Organic & Biomolecular Chemistry. 17:7531-7535
The stereoselective synthesis of glycosyl chlorides using catalytic Appel conditions is described. Good yields of α-glycosyl chlorides were obtained using a range of glycosyl hemiacetals, oxalyl chloride and 5 mol% Ph3PO. For 2-deoxysugars treatment
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f30745d2247f99d6abfe486e9eb95534
https://doi.org/10.1039/c9ob01544b
https://doi.org/10.1039/c9ob01544b
Autor:
Avene C. Colgan, Raffael C. Wende, Peter R. Schreiner, Dominik Niedek, Alexander Seitz, Emily Roesner, Eoghan M. McGarrigle, Christopher Topp
Publikováno v:
The Journal of organic chemistry. 86(5)
Herein, we report the oligopeptide-catalyzed site-selective acylation of partially protected monosaccharides. We identified catalysts that invert site-selectivity compared to N-methylimidazole, whi...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b60bb3ffc53e610e40fc97a1c87cd28
https://pubmed.ncbi.nlm.nih.gov/33617252
https://pubmed.ncbi.nlm.nih.gov/33617252
Publikováno v:
Organic letters. 22(21)
An S-selective arylation of pyridylsulfides with good functional group tolerance was developed. To demonstrate synthetic utility, the resulting pyridylsulfonium salts were used in a scalable transition-metal-free coupling protocol, yielding functiona
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22e03a2f52c901d6ec704c6312d98c4c
https://pubmed.ncbi.nlm.nih.gov/33090810
https://pubmed.ncbi.nlm.nih.gov/33090810
An S-selective arylation of pyridylsulfides with good functional group tolerance has been developed. The resulting pyridylsulfonium salts have been used in a scalable transition metal-free coupling protocol yielding functionalized bipyridine scaffold
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::579e33fd346f3cae5492b2f0efd283a4
https://doi.org/10.26434/chemrxiv.12252041.v1
https://doi.org/10.26434/chemrxiv.12252041.v1
Autor:
Susan E. Brockerhoff, Gabriel H. Travis, Joanna J. Kaylor, Eoghan M. McGarrigle, Diego Cobice, Dionissia A. Pepe, Breandán N. Kennedy, James B. Hurley, Rebecca Ward
Cone photoreceptors in the retina enable vision over a wide range of light intensities. However, the processes enabling cone vision in bright light (i.e. photopic vision) are not adequately understood. Chromophore regeneration of cone photopigments m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4790b98fc8ab067a4411bd208d97a57e
https://doi.org/10.1101/2020.02.15.950915
https://doi.org/10.1101/2020.02.15.950915