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Role of oxygen-containing functional groups in forest fire-generated and pyrolytic chars for immobilization of copper and nickel.The characterisation of two halogenated cathinone analogues: 3,5-difluoromethcathinone and 3,5-dichloromethcathinone.Identification of the novel synthetic cannabimimetic 8-quinolinyl 4-methyl-3-(1-piperidinylsulfonyl)benzoate (QMPSB) and other designer drugs in herbal incense.Detection and metabolic investigations of a novel designer steroid: 3-chloro-17α-methyl-5α-androstan-17β-ol.3α-Azido-5-cholestene.Crystallographic characterization of the first reported crystalline form of the potent hallucinogen (R)-2-amino-1-(8-bromobenzo[1,2-b;5,4-b']difuran-4-yl)propane or 'bromodragonfly': the 1:1 anhydrous proton-transfer compound with 3,5-dinitrosalicylMolecular composition of recycled organic wastes, as determined by solid-state 13C NMR and elemental analyses.Structural and solid state 31P NMR studies of the four-coordinate copper(I) complexes [Cu(PPh3)3X] and [Cu(PPh3)3(CH3CN)]X.Mitsunobu dehydration of N-Boc neomycin B.Yellow-Emitting Carbon Nanodots and Their Flexible and Transparent Films for White LEDs.Direct Mitsunobu monoesterification of N-protected tobramycin competes with intramolecular pyrrolidine formation in ester prodrug synthesis.A 13C NMR study of decomposing logging residues in an Australian hoop pine plantationMultisite Modification of Neomycin B: Combined Mitsunobu and Click Chemistry ApproachTranslational Isomerism in Some Two- and Three-Station [2]Rotaxanes†Probing Molecular Shape. 1. Conformational Studies of 5-Hydroxyhexahydropyrimidine and Related CompoundsRecognition of Bipyridinium-Based Derivatives by Hydroquinone- and/or Dioxynaphthalene-Based Macrocyclic Polyethers: From Inclusion Complexes to the Self-Assembly of [2]Catenanes†
P50
Q31141984-C2482E1D-3A30-4D3D-97E8-9F542D190556Q34233140-C3CF106B-FAFE-49FA-8D77-756873151D3DQ34510281-93E53E0B-197F-4B13-BB83-9286A070A1B7Q38756621-B97ED9F6-89BC-4919-8680-881A273FF37BQ42404780-1667A853-18A0-4824-BFE1-1412E714259FQ43074121-C7B9AE70-CF6D-4431-8601-0906EC0A6F76Q43361842-E1FC30A5-4608-40D1-972E-3EA3AAE4C38EQ46605036-59E8F964-694B-4C03-8DF3-861E54AB4863Q46853816-058A2755-39B0-4276-9D6E-805DCCDA7B13Q50193278-BB02DAD0-C50F-4474-A860-16AC0D52939EQ53091503-6CD2E490-E678-4A8F-B027-0DCD4850D56AQ58382080-3E483B85-105D-4EC2-86FC-306EDC6F0E54Q59710827-3468DF9F-DAA5-4D47-8866-19A9EC9D3FAAQ60338796-56E518BF-05B9-4B04-A123-A5C668C16CFDQ62806552-C46C5D93-0C2F-49E2-B517-33074DD03CA6Q62806774-36A60C9B-B7A9-4A4C-B200-A38C9C29D755
P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Sue E Boyd
@ast
Sue E Boyd
@en
Sue E Boyd
@es
Sue E Boyd
@nl
Sue E Boyd
@sl
type
label
Sue E Boyd
@ast
Sue E Boyd
@en
Sue E Boyd
@es
Sue E Boyd
@nl
Sue E Boyd
@sl
prefLabel
Sue E Boyd
@ast
Sue E Boyd
@en
Sue E Boyd
@es
Sue E Boyd
@nl
Sue E Boyd
@sl
P1053
J-4528-2015
P106
P21
P31
P3829
P496
0000-0003-1086-8973