Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Christopher Cooze"'
Autor:
Markus D Schoetz, Christopher Cooze, Rylan J. Lundgren, Bohdan Sosunovych, Wesley McNutt, Svetlana Grigoryan
Publikováno v:
Journal of the American Chemical Society. 143:10770-10777
Metal-catalyzed enantioselective conjugate additions are highly reliable methods for stereoselective synthesis; however, multicomponent reactions that are initiated by conjugate arylation of acyclic π-systems are rare. These reactions generally proc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b942b3dea638787dceec9a707d57f03f
https://doi.org/10.1021/jacs.1c05427
https://doi.org/10.1021/jacs.1c05427
Autor:
Braeden Mair, Michael G. J. Doyle, Rylan J. Lundgren, Armin Bauer, Benjamin H. Rotstein, Volker Derdau, Odey Bsharat, Christopher Cooze, Duanyang Kong, Maxime Munch
a-Amino acids are among the essential chemical building blocks of life. These structures are embedded in many small molecule pharmaceuticals and are the primary components of peptide-based therapeutics and biologics. Isotopically labeled a-amino acid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1f37e4b611dd33f43bf34c4835c8bf1
https://doi.org/10.26434/chemrxiv-2021-j4prf
https://doi.org/10.26434/chemrxiv-2021-j4prf
Publikováno v:
Angewandte Chemie International Edition. 58:12246-12251
Methods for the addition of unsaturated nucleophiles to carbonyls to generate Z-olefin products remain rare and often require either alkyl borane or zinc reductants, limiting their utility. Demonstrated here is that formic acid mediates the Rh-cataly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2283bdc8472d11e4daf4be1614b17c94
https://doi.org/10.1002/anie.201905540
https://doi.org/10.1002/anie.201905540
Autor:
Rylan Lundgren, Svetlana Grigoryan, Bohdan Sosunovych, Markus Schoetz, Wesley McNutt, Christopher Cooze
Metal-catalyzed enantioselective conjugate additions are highly reliable methods for stereoselective synthesis, however multi-component reactions that are initiated by conjugate arylation of acyclic p-systems are rare. These processes generally proce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99e7c81c0d5a871b0a66f05c70946991
https://doi.org/10.26434/chemrxiv.14676528
https://doi.org/10.26434/chemrxiv.14676528
Metal-catalyzed enantioselective conjugate additions are highly reliable methods for stereoselective synthesis, however multi-component reactions that are initiated by conjugate arylation of acyclic p-systems are rare. These processes generally proce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c45bbc0c3de2d8847cf7a7e67c09a55d
https://doi.org/10.26434/chemrxiv.14676528.v1
https://doi.org/10.26434/chemrxiv.14676528.v1
Autor:
Maxime Munch, Odey Bsharat, Michael Doyle, Braeden Mair, Christopher Cooze, Duanyang Kong, Rylan Lundgren, Benjamin Rotstein
Publikováno v:
Nuclear Medicine and Biology. :S29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e693d641815c41d0ed63e8d3a38d04a
https://doi.org/10.1016/s0969-8051(22)00100-7
https://doi.org/10.1016/s0969-8051(22)00100-7
Autor:
Rylan J. Lundgren, Qiqige Qiqige, Maxime Munch, Benjamin H. Rotstein, Christopher Cooze, Duanyang Kong
Carbazole/cyanobenzene photocatalysts promote the direct isotopic carboxylate exchange of C(sp3 )-acids with labelled CO2. Substrates that are not compatible with transition metal catalyzed degradation-reconstruction approaches or prone to thermally
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1838982b0290ffb1d73f6fe9afa9681c
https://doi.org/10.26434/chemrxiv.13111505.v1
https://doi.org/10.26434/chemrxiv.13111505.v1
Publikováno v:
Synlett. 28:2928-2932
Concise syntheses of the polyketide natural product (–)-muricatacin and (–)-(R,R)-L-factor (natural product enantiomer) were achieved in four steps by employing an organocatalytic asymmetric direct vinylogous aldol reaction of γ-crotonolactone a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a960b81f58c68fa120bdd4428d771a7
https://doi.org/10.1055/s-0036-1590858
https://doi.org/10.1055/s-0036-1590858
We demonstrate that formic acid mediates the Rh-catalyzed, Z-selective coupling of dienes and aldehydes. The process is distinguished by broad tolerance towards reducible or electrophilic groups. Kinetic analysis suggests that generation of the catal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c86073f3d01315c8d6f9e22ed6216efd
https://doi.org/10.26434/chemrxiv.8081174
https://doi.org/10.26434/chemrxiv.8081174
We demonstrate that formic acid mediates the Rh-catalyzed, Z-selective coupling of dienes and aldehydes. The process is distinguished by broad tolerance towards reducible or electrophilic groups. Kinetic analysis suggests that generation of the catal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36cf9831937453687c1da424bd7a468d
https://doi.org/10.26434/chemrxiv.8081174.v1
https://doi.org/10.26434/chemrxiv.8081174.v1