Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Spencer Langevin"'
Publikováno v:
BMC Ophthalmology, Vol 20, Iss 1, Pp 1-3 (2020)
Abstract Background Bilateral Acute Depigmentation of the Iris (BADI) is a condition which was first described in a case series from Turkey by Tugal-Tutkin and Urgancioglu in (Graefes Arch Clin Exp Ophthalmol 244:742-6, 2006). The condition is charac
Externí odkaz:
https://doaj.org/article/b4547bbbb5d84d86aa854929b2aae400
Autor:
Helen Chioma Okoh, Sandeep Singh Lubana, Spencer Langevin, Susan Sanelli-Russo, Adriana Abrudescu
Publikováno v:
Case Reports in Rheumatology, Vol 2015 (2015)
Systemic lupus erythematosus (SLE) is an autoimmune systemic disease with multiple organ involvement with high morbidity and mortality rate. Among the severe potential fatal complications are those of the central and peripheral nervous system which u
Externí odkaz:
https://doaj.org/article/daa898af04384c48bc32eb0eca673bb0
Autor:
Nicholas Kantack, Spencer Langevin, Tessa VanVolkenburg, Jennifer Skerritt Benzing, Zhiyong Xia, Raymond Hoheisel, James MacMahan, Sean Brown
Publikováno v:
OCEANS 2021: San Diego – Porto.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c1631d8c371280da3dbfc94b2c3de8b
https://doi.org/10.23919/oceans44145.2021.9705686
https://doi.org/10.23919/oceans44145.2021.9705686
Publikováno v:
New Journal of Chemistry. 43:5282-5286
Functionalized izidinones and isoquinolones are commonplace motifs in bioactive molecules. Here, we describe a direct and modular approach to [6,n] and [7,n]-1-azabicyclic unsaturated lactams, most of which bear at least one endocyclic heteroatom. A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ac851a402b6a5d9303496862b5acae8
https://doi.org/10.1039/c8nj06539j
https://doi.org/10.1039/c8nj06539j
Autor:
Adam Rozman, Avra Kundu, Leslie Hamilton, Spencer Langevin, Swaminathan Rajaraman, Julia B. Patrone
Publikováno v:
Journal of Micromechanics and Microengineering. 31:075007
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e19d6fdcd8333206ff3304b1b2dd29a3
https://doi.org/10.1088/1361-6439/ac0322
https://doi.org/10.1088/1361-6439/ac0322
Publikováno v:
Organic & Biomolecular Chemistry. 15:1217-1221
A high-yielding, cost-effective, modular and environmentally benign approach to [5,5]- or [6,5]-2-azabicyclic architectures bearing vicinal stereocenters, by Fe-catalyzed intramolecular dehydrative coupling of readily affordable alcohol-bearing allyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64af7fdc3beb2e31ecaf62a7bb749fcf
https://doi.org/10.1039/c6ob02652d
https://doi.org/10.1039/c6ob02652d
Publikováno v:
Retinal casesbrief reports. 13(3)
To describe a case of serous retinopathy and associated photoreceptor atrophy after intravenous cisplatin therapy.Evaluation was performed using electroretinogram, optical coherence tomography, fundus autofluorescence, and funduscopic examinations to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40e31753276873d1bcc908b10b1e30fc
https://pubmed.ncbi.nlm.nih.gov/28333855
https://pubmed.ncbi.nlm.nih.gov/28333855
Publikováno v:
ChemInform. 47
The synthesis of α-aryl and alkenyl pyrrolidine-, piperidine-, and azepane derivatives, through the intermediacy of cyclic enamides is described. The desired outcome is achieved through ruthenium-catalyzed, site-selective sp2 C–H activation/cross-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84eb7f368506cc82c2c6899df9b26c81
https://doi.org/10.1002/chin.201620046
https://doi.org/10.1002/chin.201620046
Publikováno v:
Organicbiomolecular chemistry. 14(3)
The synthesis of α-aryl and alkenyl pyrrolidine-, piperidine-, and azepane derivatives, through the intermediacy of cyclic enamides is described. The desired outcome is achieved through ruthenium-catalyzed, site-selective sp(2) C-H activation/cross-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a08488ebdb26910824a1a965ed275cd0
https://pubmed.ncbi.nlm.nih.gov/26612230
https://pubmed.ncbi.nlm.nih.gov/26612230