Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Edward J. McCLAIN"'
Autor:
Boyle C. Cheng, Isaac R. Swink, Cooper T. Cheng, Owen G. Corcoran, Vicki Z. Wang, Edward J. McClain, Praveer S. Vyas, Izzy Owen, Chen Xu, Daniel T. Altman, Alexander K. Yu
Publikováno v:
Bioengineering, Vol 11, Iss 9, p 898 (2024)
P-15 is a 15-amino-acid-long biomimetic peptide widely demonstrated to enhance osteogenesis in vivo. Despite the prevalence of polyether-ether-ketone (PEEK) in interbody device manufacturing, a growing body of evidence suggests it may produce an unfa
Externí odkaz:
https://doaj.org/article/bf5cc3db2b224d8bb4bd052a137ca545
Autor:
Amol H. Trivedi, Vicki Z. Wang, Edward J. McClain, Praveer S. Vyas, Isaac R. Swink, Edward D. Snell, Boyle C. Cheng, Patrick J. DeMeo
Publikováno v:
Biomedicines, Vol 12, Iss 7, p 1544 (2024)
Musculoskeletal (MSK) pathology encompasses an array of conditions that can cause anything from mild discomfort to permanent injury. Their prevalence and impact on disability have sparked interest in more effective treatments, particularly within ort
Externí odkaz:
https://doaj.org/article/6323bb34bfab4bec875ce78b8f0ef1ae
Autor:
Longbo Li, Bianca Matsuo, Guillaume Levitre, Edward J. McClain, Eric A. Voight, Erika A. Crane, Gary A. Molander
Publikováno v:
Chemical Science. 14:2713-2720
Diverse DNA-encoded libraries of complex and novel sp3-rich spirocycles were achieved using a versatile and operationally simple visible light-mediated intermolecular [2 + 2] cycloaddition.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ca9f354518d32b785d8ddc6a587a4d4b
https://doi.org/10.1039/d3sc00144j
https://doi.org/10.1039/d3sc00144j
Autor:
Expédite Yen-Pon, Longbo Li, Guillaume Levitre, Jadab Majhi, Edward J. McClain, Eric A. Voight, Erika A. Crane, Gary A. Molander
Publikováno v:
Journal of the American Chemical Society. 144:12184-12191
DNA-encoded libraries have proven their tremendous value in the identification of new lead compounds for drug discovery. To access libraries in new chemical space, many methods have emerged to transpose traditional mol-scale reactivity to nmol-scale,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bb4dda02c8cc1d32a7f8a6798a63669
https://doi.org/10.1021/jacs.2c03025
https://doi.org/10.1021/jacs.2c03025
Autor:
Boyle C. Cheng, Isaac Swink, Edward J. McClain, Praveer S. Vyas, Thomas Muzzonigro, Jake Carbone, Ali Zaidi, Jason Long, Daniel T. Altman, Alexander K. Yu
Publikováno v:
Spine.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2cf8bfd25e0530749c204f5dc65e97c5
https://doi.org/10.1097/brs.0000000000004594
https://doi.org/10.1097/brs.0000000000004594
Publikováno v:
Chemical science. 13(41)
Recent advances in synthetic chemistry have seen a resurgence in the development of methods for visible light-mediated radical generation. Herein, we report the development of a photoactive ester based on a quinoline
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50944fa11839267e0ed3204cbcb38dea
https://pubmed.ncbi.nlm.nih.gov/36349097
https://pubmed.ncbi.nlm.nih.gov/36349097
Publikováno v:
ACS Catalysis. 10:12636-12641
Electron donor–acceptor (EDA) complexes can controllably generate radicals under mild conditions through selective photoexcitation events. However, unproductive reactivity from fast deactivation of...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9bc65f5dfdae6f5d35de73475fb32595
https://doi.org/10.1021/acscatal.0c03837
https://doi.org/10.1021/acscatal.0c03837
Publikováno v:
Journal of the American Chemical Society. 141:8914-8920
This paper describes the one-electron interconversions of isolable NiIII and NiIV complexes through their reactions with carbon-centered radicals (R•). First, model NiIII complexes are shown to react with alkyl and aryl radicals to afford NiIV prod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d1ddccf8dd8c609cb015a1a0fb527c9
https://doi.org/10.1021/jacs.9b02411
https://doi.org/10.1021/jacs.9b02411
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
Electron donor-acceptor (EDA) complexes can controllably generate radicals under mild conditions through selective photoexcitation events. However, unproductive reactivity from fast deactivation of the photoexcited complexes through back electron tra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::969896c58bcc569b6265961fe22c3ab5
https://doi.org/10.26434/chemrxiv.12130011.v1
https://doi.org/10.26434/chemrxiv.12130011.v1
