Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Katie A, Rykaczewski"'
Autor:
Katie A. Rykaczewski, Marc R. Becker, Manasi J. Anantpur, Rosario C. Sausa, Eric C. Johnson, Joshua A. Orlicki, Eric J. Bukowski, Jesse J. Sabatini, Corinna S. Schindler
Publikováno v:
Journal of the American Chemical Society. 144(41)
Despite their favorable properties, azetidines are often overlooked as lead compounds across multiple industries. This is often attributed to the challenging synthesis of densely functionalized azetidines in an efficient manner. In this work, we repo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30a88b9410e7ddba0ecc00a4753594ed
https://pubmed.ncbi.nlm.nih.gov/36197722
https://pubmed.ncbi.nlm.nih.gov/36197722
Publikováno v:
Organic Letters. 22:6516-6519
One of the most efficient ways to synthesize oxetanes is the light-enabled [2 + 2] cycloaddition reaction of carbonyls and alkenes, referred to as the Paternò-Büchi reaction. The reaction conditions for this transformation typically require the use
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8959c47c193ed8727638adeb0a92a1c3
https://doi.org/10.1021/acs.orglett.0c02316
https://doi.org/10.1021/acs.orglett.0c02316
Autor:
Troy E. Zehnder, Katie A. Rykaczewski, Mario A. Gaviria, Hannah L. Vonesh, Alistair D. Richardson, Emilia J. Groso, Corinna S. Schindler
Publikováno v:
Organic Letters. 22:2844-2848
Herein we describe the application of Lewis-acid-catalyzed carbonyl–olefin metathesis toward the synthesis of substituted tetrahydropyridines from commercially available amino acids as chiral pool ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11f423b20ade2e8914361a6d4af0201e
https://doi.org/10.1021/acs.orglett.0c00918
https://doi.org/10.1021/acs.orglett.0c00918
One of the most efficient ways to synthesize oxetanes is the light-enabled [2+2] cycloaddition reaction of carbonyls and alkenes, referred to as the Paternò-Büchi reaction. The reaction conditions for this transformation typically require the use o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5cdee82f7691c3f93d10ff8a9dee327
https://doi.org/10.26434/chemrxiv.12606377.v1
https://doi.org/10.26434/chemrxiv.12606377.v1
Autor:
Katie A, Rykaczewski, Emilia J, Groso, Hannah L, Vonesh, Mario A, Gaviria, Alistair D, Richardson, Troy E, Zehnder, Corinna S, Schindler
Publikováno v:
Organic letters. 22(7)
Herein we describe the application of Lewis-acid-catalyzed carbonyl-olefin metathesis toward the synthesis of substituted tetrahydropyridines from commercially available amino acids as chiral pool reagents. This strategy relies on FeCl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::443a2aec8ed9d474d5215dbcf6f452ac
https://pubmed.ncbi.nlm.nih.gov/32202807
https://pubmed.ncbi.nlm.nih.gov/32202807
Publikováno v:
ACS Catalysis
Carbonyl-ene, Prins and carbonyl-olefin metathesis reactions represent powerful strategies for carbon-carbon bond formation relying on Lewis acid catalysts. Although common Lewis acids are able to provide efficient activation, the reactions often pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72a67e231797726b169dd1cea62a5a9c
https://zenodo.org/record/3946632
https://zenodo.org/record/3946632
Publikováno v:
Organic Syntheses
Organic Synth
Organic Synth
[Image: see text]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40d3dce83bb27be703cc1a01de54819a
https://doi.org/10.15227/orgsyn.095.0472
https://doi.org/10.15227/orgsyn.095.0472
Autor:
Hannah L. Vonesh, Corinna S. Schindler, Alistair D. Richardson, Mario A. Gaviria, Troy E. Zehnder, EmiliaJ. Groso, Katie A. Rykaczewski
Herein, we describe the application of Lewis acid-catalyzed carbonyl-olefin metathesis towards the synthesis of chiral, substituted tetrahydropyridines from commercially available amino acids as chiral pool reagents. This strategy relies on FeCl3 as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::255e8456793e9ad451e77219b347c61b
https://doi.org/10.26434/chemrxiv.10007291.v1
https://doi.org/10.26434/chemrxiv.10007291.v1
Autor:
Katie A. Rykaczewski, Lydia H. Griggs, Paxton A.M. Reed, Saumya Jain, Kate E. Sabourin, Joseph M. Langenhan, Paul J. Goo
Publikováno v:
Carbohydr Res
Herein, we report the first selective anomeric N-acylation of a glycosylhydrazide. We show that this transformation can be harnessed to generate amino acid building blocks including FmocAsn(GlcNAc)OH (1), a residue that has been previously shown to b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f25f024e17612c7f77b8d8b6a215df6
https://doi.org/10.1016/j.carres.2020.108022
https://doi.org/10.1016/j.carres.2020.108022