Protecting communication systems from EMP effects of nuclear explosions
Antituberculosis Agents--VI. Streptidine-oxyethyl β-D-glucopyranoside
Antituberculosis Agents--V. Streptidine-β-Hexosides and Related Compounds
Dynamics of β-Lactoglobulin Penetration into Langmuir Monolayers of 2D Condensating Phospholipid
On the Occurrence of Caustics in the Drawdown Zone of Silica Fibers
The transient response of tapered transmission lines
A tapered strip line for pulse transformer service
Notes on the use of alternating current in unloading coal
13 C Nuclear Magnetic Resonance Studies. XVI. 13 C Spectra of some Substituted Acrylic Acids and their Methyl Esters. A Correlation of Olefinic Shieldings in α,β-unsaturated Carbonyl
13 C Nuclear magnetic resonance studies. XIII. 13 C Carbonyl carbon shieldings of some β,γ-unsaturated ketones
PREFERRED RESIDENCE CONFORMATIONS OF DIASTEREOISOMERIC α–β AMINO ALCOHOLS: AN N.M.R. STUDY OF THE EPHEDRINES
Nuclear magnetic resonance studies. XXXII. Rearrangement, isomerization, and deuterium exchange via β-enolization in bicyclooctenones. A 2 H nuclear magnetic resonance study
The use of electric power in the mining of anthracite coal
A synthesis of hirsutene: a simple route via β-enolization
Evidence for cyclopropoxide intermediates in α-methyl H/D exchange of cyclic ketones under homoenolization conditions
Biosynthesis of antifungal stress metabolites from potato: observation of hydride shifts via the "β-hop" from incorporation of [2- 2 H 3 ,2- 13 C]acetate and 13 Cmr
Concerning stereochemical assignments from 13 C spectra of systems experiencing γ substituent effects. Deshielding antiperiplanar interactions can mislead the unwary
13 C magnetic resonance studies 133. An examination of the effect of conformation on β-enolization in some bicyclo[3.2.1]octan-2-ones
Proton Magnetic Resonance Studies of Rotational Isomerism in Halotoluene Derivatives. IX. Rotational Barriers and Conformational Energy Differences in α,α,α′,α′,α″,α″,
The synthesis of 3,3-dimethyltricyclo[6.3.0.0 1,5 ]undecan-4-one via β-enolate rearrangement. A new approach to the pentalenene ring system