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Chemical Communications (Cambridge, England)|November 11, 2014
A new method for peptide synthesis in the N→C direction: amide assembly through silver-promoted reaction of thioamidesAysa Pourvali, James R Cochrane, Craig A HuttonOrganic Letters|September 22, 2020
Total Synthesis of the Putative Structure of Asperipin-2a and Stereochemical ReassignmentSadegh Shabani, Jonathan M White, Craig A HuttonMolecular Biosystems|June 21, 2007
Inhibition of lysine biosynthesis: an evolving antibiotic strategyCraig A Hutton, Matthew A Perugini, Juliet A GerrardChemistry (Weinheim an Der Bergstrasse, Germany)|July 29, 2025
Tetrahydropyranyl Backbone Protection for Enhanced Fmoc Solid-Phase Peptide SynthesisSamuel J Paravizzini, Craig A Hutton, John A KarasOrganic Letters|May 13, 2011
Synthesis of β,γ-dihydroxyhomotyrosines by a tandem Petasis-asymmetric dihydroxylation approachQuentin I Churches, Jonathan M White, Craig A HuttonThe Journal of Organic Chemistry|May 21, 2015
A general method for interconversion of boronic acid protecting groups: trifluoroborates as common intermediatesQuentin I Churches, Joel F Hooper, Craig A HuttonOrganic & Biomolecular Chemistry|January 21, 2025
Ag(I)-promoted fragment coupling of peptide thioamidesVarsha J Thombare, Carlie L Charron, Craig A HuttonThe Journal of Organic Chemistry|September 23, 2015
Total Synthesis of Ustiloxin D Utilizing an Ammonia-Ugi ReactionAaron L Brown, Quentin I Churches, Craig A HuttonMini Reviews in Medicinal Chemistry|February 7, 2003
Inhibitors of lysine biosynthesis as antibacterial agentsCraig A Hutton, Timothy J Southwood, Jennifer J TurnerBioorganic & Medicinal Chemistry|February 25, 2005
Heterocyclic inhibitors of dihydrodipicolinate synthase are not competitiveJennifer J Turner, Juliet A Gerrard, Craig A HuttonPageof 8