✍ Scribed by Melissa J. Heinsen; Thomas C. Pochapsky
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract Reliable methods for the selective deuteration of β‐cyclodextrin are described. Kinetic studies of the proton‐deuterium exchange catalysed by Raney nickel in deuterium oxide show dramatically different behaviours of positions 2, 6 and 3 and allow selective labelling. Deuteration of prot
## Abstract [3‐D]2‐Nitroacetophenone and [alcohol‐^18^O]‐1‐(2‐nitrophenyl)ethyl alcohol were prepared and used to synthesise labelled P^3^‐l‐(2‐nitrophenyl)ethyl esters of ATP (“caged ATP”) with isotope present either as deuterium on the 3‐position of the nitrosubstituted ring or as ^18^oxygen in t
## Abstract Four deuterium‐substituted α‐tocopherols (dideutero‐__RRR__, nonadeutero‐__ambo__, nonadeutero‐__all‐rac__ and undecadeutero‐__all‐rac__) and a dideutero‐__RRR__‐γ‐tocopherol have been synthesized for use in studies of the biokinetics, bioavailability and metabolism of vitamin E.
Deuterium labelled thiomuscimol ( 6 ) was synthesized v i a zatalytic deuteration in strongly basic CZH302H-'H 0 (9:l) of 3-methoxy-4-bromo-5-(N-meth-oxycarbonyZaminomethy1) isothiazole ( 3 ) . ment of bromine by deuterium was accompanied by partial exchange of the side chain methylene protons for d