Zobrazeno 1 - 10
of 63
pro vyhledávání: '"Jolene P. Reid"'
Autor:
Jolene P. Reid
Publikováno v:
Communications Chemistry, Vol 4, Iss 1, Pp 1-4 (2021)
The transfer of chiral information from optically pure reaction components to products can generate enantiomerically-enriched molecules, but the control of stereochemistry often proves challenging. Here, the author highlights how our fundamental unde
Externí odkaz:
https://doaj.org/article/990e07f553214477937bd125ddb95aa4
Autor:
Madhureeta Das Gupta, Charlotte E. Boott, Jennifer E. Goon, Brian O. Patrick, Jolene P. Reid, Mark J. MacLachlan
Publikováno v:
ACS Applied Nano Materials. 6:4672-4680
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d49aebaa05aaa88dd44eea85d961e01
https://doi.org/10.1021/acsanm.3c00159
https://doi.org/10.1021/acsanm.3c00159
Publikováno v:
Chemical Science. 14:1885-1895
Statistical models can be applied to predict and develop enantioselective reactions involving two catalysts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03c0929a4c519eb40cb3f7d3237de3ec
https://doi.org/10.1039/d2sc05974f
https://doi.org/10.1039/d2sc05974f
Autor:
Jolene P. Reid, Jianyu Zhai
Publikováno v:
Synlett. 34:1174-1184
Recent strategies for enantioinduction often focus on employing a chiral catalyst to noncovalently interact with the substrate. By restricting the number of low energy diastereomeric transition states the reacting components can adopt, stereoselectiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e4b496f5ac44b2a73734f83df8524935
https://doi.org/10.1055/a-1957-3872
https://doi.org/10.1055/a-1957-3872
Autor:
Phillip M. Danby, Andrew Jeong, Lyann Sim, Ryan P. Sweeney, Jacob F. Wardman, Ryan Karimi, Andreas Geissner, Liam J. Worrall, Jolene. P. Reid, Natalie C. J. Strynadka, Stephen G. Withers
Publikováno v:
Angewandte Chemie International Edition. 62
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bee0f83f9281e230b316601300a52dd
https://doi.org/10.1002/anie.202301258
https://doi.org/10.1002/anie.202301258
Publikováno v:
Organic Letters. 24:1429-1433
Practitioners are generally not willing to explore modern reactions where considerable synthetic effort is required to generate materials and the results are not certain. Organocatalysis exemplifies this, in which a broad set of enantioselective reac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f20273e2f74bcf106f7aa129242a1b99
https://doi.org/10.1021/acs.orglett.1c04134
https://doi.org/10.1021/acs.orglett.1c04134
Publikováno v:
ACS Catalysis. 11:11897-11905
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9489dd4b96bb61ba6a724f88a900e14
https://doi.org/10.1021/acscatal.1c03520
https://doi.org/10.1021/acscatal.1c03520
Autor:
Junshan Lai, Jolene P. Reid
Publikováno v:
Chemical science. 13(37)
CH⋯O bonds are a privileged noncovalent interaction determining the energies and geometries of a large number of structures. In catalytic settings, these are invoked as a decisive feature controlling many asymmetric transformations involving aldehy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35aa3e8a071156292cb0454db428ee77
https://pubmed.ncbi.nlm.nih.gov/36320465
https://pubmed.ncbi.nlm.nih.gov/36320465
Autor:
Jolene P. Reid, Matthew S. Sigman
Publikováno v:
Nature
Summary: When faced with unfamiliar reaction space, synthetic chemists typically apply reported conditions (reagents, catalyst, solvent, additives) from closely-related reactions to new substrate types. Unfortunately, this approach often fails due to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac4ac7a175528c3541d2a09834406f47
http://europepmc.org/articles/PMC6641578
http://europepmc.org/articles/PMC6641578