Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Rory C. McAtee"'
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-8 (2020)
Arene dearomatization reactions allow chemists to rapidly build unique chemical architectures from largely available starting materials. Here, the authors show a photocatalytic carboamination/dearomatization cascade process leading to 1,4-cyclohexadi
Externí odkaz:
https://doaj.org/article/fab209fa1c37460da0791187c95c689d
Autor:
Daryl Staveness, Mikaela Breunig, Viviana Ortiz, Hyunkyu Sang, James L. Collins, III, Rory C. McAtee, Martin I. Chilvers, Corey R.J. Stephenson
Publikováno v:
Cell Reports Physical Science, Vol 2, Iss 9, Pp 100548- (2021)
Summary: Agrochemical fungicidal leads have been prepared from photochemically derived 1-aminonorbornane building blocks. The unique 1-aminonorbornane core is generated via direct excitation of a Schiff base precursor, leveraging the N-centered radic
Externí odkaz:
https://doaj.org/article/1e5c9cd9e2334b2caae663011cb777c9
Autor:
Christopher C. McAtee, Daniel J. Nasrallah, Ho Ryu, Michael R. Gatazka, Rory C. McAtee, Mu-Hyun Baik, Corinna S. Schindler
Publikováno v:
ACS Catalysis. 13:3036-3043
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d48883cb7a2864f56d5322de2f862949
https://doi.org/10.1021/acscatal.2c05535
https://doi.org/10.1021/acscatal.2c05535
Autor:
Anthony R. Allen, Jia-Fei Poon, Rory C. McAtee, Nicholas B. Watson, Derek A. Pratt, Corey R.J. Stephenson
Publikováno v:
ACS catalysis. 12(14)
Alkene aminoarylation with arylsulfonylacetamides via a visible-light mediated radical Smiles-Truce rearrangement represents a convenient approach to the privileged arylethylamine pharmacaphore traditionally generated by circuitous, multi-step sequen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63bca62a80c1d9c18aeeeec79508f82c
https://pubmed.ncbi.nlm.nih.gov/36312445
https://pubmed.ncbi.nlm.nih.gov/36312445
Autor:
Rory C. McAtee, Mikaela Breunig, Daryl Staveness, Martin I. Chilvers, Viviana Ortiz, Hyunkyu Sang, James L. Collins, Corey R. J. Stephenson
Publikováno v:
Cell Reports Physical Science, Vol 2, Iss 9, Pp 100548-(2021)
Cell reports. Physical science
Cell reports. Physical science
SUMMARY Agrochemical fungicidal leads have been prepared from photochemically derived 1-aminonorbornane building blocks. The unique 1-aminonorbornane core is generated via direct excitation of a Schiff base precursor, leveraging the N-centered radica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38af58a3c781a0a52b09d5073b32bc17
http://www.sciencedirect.com/science/article/pii/S2666386421002599
http://www.sciencedirect.com/science/article/pii/S2666386421002599
Publikováno v:
Angew Chem Int Ed Engl
This report details the development of a masked N-centered radical strategy that harvests the energy of light to drive the conversion of cyclopropylimines to 1-aminonorbornanes. This process employs the N-centered radical character of a photoexcited
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4680579ab89a6f40d3a2cbf7e67cf9bb
https://doi.org/10.1002/anie.201909492
https://doi.org/10.1002/anie.201909492
Publikováno v:
Trends Chem
Over the past decade, photoredox catalysis has risen to the forefront of synthetic organic chemistry as an indispensable tool for selective small-molecule activation and chemical-bond formation. This cutting-edge platform allows photosensitizers to c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b137c1e3d34dca57210d66b21e1819ca
https://doi.org/10.1016/j.trechm.2019.01.008
https://doi.org/10.1016/j.trechm.2019.01.008
Publikováno v:
Tetrahedron. 74:3306-3313
We report herein the intramolecular α-tert-alkylation of unsaturated β-ketoesters which gives rise to highly functionalized cyclopentanes. This strategy is characterized by its operational simplicity, mild reaction conditions and the use of scandiu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::050e9edc9a60d1c90b2bcf2aa33f3799
https://doi.org/10.1016/j.tet.2018.04.036
https://doi.org/10.1016/j.tet.2018.04.036
Autor:
Michael S. Wang, Andrew T. Franks, Kacey C. Hall, Rory C. McAtee, Vivian I. Lu, Katherine J. Franz
Publikováno v:
Photochemical & Photobiological Sciences. 16:1604-1612
The range of applications for photoswitching moieties is diverse, and the ability to design switches with variable photochemical and physical properties is consequently important for realizing their potential. Previously we reported on the photochrom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c9b0408aa386beafdb482de4a97e394
https://doi.org/10.1039/c7pp00173h
https://doi.org/10.1039/c7pp00173h
This report details the development of a masked N-centered radical strategy that harvests the chemical potential of violet light to drive the conversion of cyclopropylimines to 1-aminonorbornanes. This process is initiated by the nitrogen-centered ra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a5199ed71b9da220f7b841b122353e2
https://doi.org/10.26434/chemrxiv.7390421.v1
https://doi.org/10.26434/chemrxiv.7390421.v1
