Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Elisa G. Gutierrez"'
Publikováno v:
Organic Letters. 13:5754-5757
The indium(III)-catalyzed enantioselective and regioselective addition of pyrroles to isatins is described. The effects of metal and solvent on the reactivity and selectivity are compared and discussed, demonstrating that the indium(III)-indapybox co
Autor:
Anna G. Wenzel, Eric J. Moorhead, Eva H. Smith, Vivian S. Lin, Victoria L. Sun, Laura K. G. Ackerman, Sharday Grant, Claire E. Knezevic, Elisa G. Gutierrez
Publikováno v:
European Journal of Organic Chemistry. 2010:3027-3031
Facile synthetic routes to a chiral chloro-substituted biphenyl-2,2′-diyl hydrogen phosphate and a chiral O,O-biphenyl-2,2′-diyl phosphoramidothioate are described. The performance of these compounds as catalysts for the hydrophosphonylation of i
Autor:
Joshua A. Buss, Eric J. Moorhead, Anna G. Wenzel, Elisa G. Gutierrez, Sharday Grant-Overton, Eva H. Smith, Vivian S. Lin
Publikováno v:
ChemInform. 46
An efficient protocol for the oxidative coupling of phenols and naphthols is developed and compared with other oxidative coupling methodologies.
Autor:
Vivian S. Lin, Elisa G. Gutierrez, Joshua A. Buss, Eva H. Smith, Eric J. Moorhead, Anna G. Wenzel, Sharday Grant-Overton
The tert-butyl peroxide-initiated, oxidative coupling of phenols can frequently promote reactions that otherwise perform poorly under alternative conditions. Despite this utility, peroxide coupling reactions employing conventional heat often require
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4629ad38eb58484e48e4a0a077a884bb
Autor:
Annaliese K. Franz, Elisa G. Gutierrez
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[91-56-5] C8H5NO2 (MW 147.13) InChI = 1S/C8H5NO2/c10-7-5-3-1-2-4-6(5)9-8(7)11/h1-4H,(H,9,10,11) InChIKey = JXDYKVIHCLTXOP-UHFFFAOYSA-N (reagent used primarily as an electrophilic component in a wide array of reactions) Physical Data: mp 193–195 °C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::38366a010935277de515c383e4ae907b
https://doi.org/10.1002/047084289x.rn01611
https://doi.org/10.1002/047084289x.rn01611
Autor:
Jerry L. Dallas, Dirk M. Holstege, Prokopios Magiatis, James R. Millam, Jennifer C. Brennan, Anatoly A. Soshilov, Elisa G Gutierrez, Michael S. Denison
Publikováno v:
BMC Complementary and Alternative Medicine
Brennan, Jennifer C; Denison, Michael S; Holstege, Dirk M; Magiatis, Prokopios; Dallas, Jerry L; Gutierrez, Elisa G; et al.(2013). 2,3-cis-2R,3R-(¿)-epiafzelechin-3-O-p-coumarate, a novel flavan-3-ol isolated from Fallopia convolvulus seed, is an estrogen receptor agonist in human cell lines. BMC Complementary and Alternative Medicine, 13(1), 133. doi: http://dx.doi.org/10.1186/1472-6882-13-133. Retrieved from: http://www.escholarship.org/uc/item/4w07503w
Brennan, Jennifer C; Denison, Michael S; Holstege, Dirk M; Magiatis, Prokopios; Dallas, Jerry L; Gutierrez, Elisa G; et al.(2013). 2,3-cis-2R,3R-(¿)-epiafzelechin-3-O-p-coumarate, a novel flavan-3-ol isolated from Fallopia convolvulus seed, is an estrogen receptor agonist in human cell lines. BMC Complementary and Alternative Medicine, 13(1), 133. doi: http://dx.doi.org/10.1186/1472-6882-13-133. Retrieved from: http://www.escholarship.org/uc/item/4w07503w
Background The plant genus Fallopia is well-known in Chinese traditional medicine and includes many species that contain bioactive compounds, namely phytoestrogens. Consumption of phytoestrogens may be linked to decreased incidence of breast and pros
Publikováno v:
ChemInform. 43
The reaction requires an excess of pyrrole to provide the addition products with high yields and enantioselectivities.
Autor:
Eric J. Moorhead, Eva H. Smith, Claire E. Knezevic, Elisa G. Gutierrez, Vivian S. Lin, Anna G. Wenzel, Victoria L. Sun, Laura K. G. Ackerman, Sharday Grant
Publikováno v:
ChemInform. 41
Facile synthetic routes to a chiral chloro-substituted biphenyl-2,2′-diyl hydrogen phosphate and a chiral O,O-biphenyl-2,2′-diyl phosphoramidothioate are described. The performance of these compounds as catalysts for the hydrophosphonylation of i