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Chemistry (Weinheim an Der Bergstrasse, Germany)|February 3, 2015
From minutes to years: predicting organotrifluoroborate solvolysis ratesZhibo Liu, Daniel Chao, Ying Li, et al.Current Opinion in Chemical Biology|April 24, 2018
Organotrifluoroborates as prosthetic groups for Single-Step F18-Labeling of Complex MoleculesDavid M PerrinMedical Hypotheses|December 1, 2020
A hypothesis for examining dihydroxyacetone, the active component in sunless tanning products, as a topical prophylactic against SARS-COV-2 transmissionDavid M PerrinAccounts of Chemical Research|April 8, 2016
[(18)F]-Organotrifluoroborates as Radioprosthetic Groups for PET Imaging: From Design Principles to Preclinical ApplicationsDavid M PerrinThe Journal of Organic Chemistry|May 21, 2008
Substituent effects on aryltrifluoroborate solvolysis in water: implications for Suzuki-Miyaura coupling and the design of stable (18)F-labeled aryltrifluoroborates for use in PET imagingRichard Ting, Curtis W Harwig, Justin Lo, et al.Bioconjugate Chemistry|January 22, 2004
Efficient synthesis of isotopically pure isotope-coded affinity tagging reagentsAnupama Patel, David M PerrinMethods in Enzymology|June 2, 2020
FlICk (fluorescent isoindole crosslinking) for peptide staplingMihajlo Todorovic, David M PerrinChemistry (Weinheim an Der Bergstrasse, Germany)|February 20, 2008
Intraannular Savige-Fontana reaction: one-step conversion of one class of monocyclic peptides into another class of bicyclic peptidesJonathan P May, David M PerrinBioorganic & Medicinal Chemistry Letters|August 4, 2010
Introduction of guanidinium-modified deoxyuridine into the substrate binding regions of DNAzyme 10-23 to enhance target affinity: implications for DNAzyme designCurtis H Lam, David M PerrinPageof 18