Sentence examples for asymmetric step from inspiring English sources

The implementation of the algorithm led to asymmetric step sizes.

The synthesis employs a molybdenum-catalyzed asymmetric allylic alkylation of an oxindole nucleophile and a monosubstituted allylic electrophile as a key asymmetric step.

With this powerful asymmetric methodology in hand, we planned to utilize our Mo-AAA methodology as a key asymmetric step to construct one of the two quaternary stereocenters in -perophoramidine (1).

Herein we describe a catalytic asymmetric total synthesis –perophoramidine (1) based on a different strategy, which utilizes a molybdenum-catalyzed asymmetric allylic alkylation (Mo-AAA) as a key asymmetric step to create one quaternary stereocenter and an unusual regio- and diastereoselective allylation of an imino ether enolate, which constructs the other quaternary stereocenter in the target.

This diplexer consists of two bandpass filters based on the triangular open loop asymmetric stepped impedance resonator in order to have a small size as well as simple structure.

The corrected width is 14.6 (10.5–21.5) km for the sigmoid model whereas the asymmetric stepped cline width falls within the support interval 0.1 6.4 km, with the stepped hypothesis justified in comparison to the sigmoid one (ΔLL = 8.58; df = 4 ; P = 0.002).

Measuring cline widths using the software Analyse (see Methods), the width of the Y cline along this consensus orientation is estimated at 28.1 km (lower and upper bounds: 19.5 43.5) for the sigmoid model and 19.0 (14.5–25.6) km for the asymmetric stepped model, with little justification for the complicated step hypothesis compared to the simpler sigmoid change.

The sample studied here is asymmetric In0.15Ga0.85As/GaAs/Al0.3Ga0.7As step QWs grown on (001) SI-GaAs substrate by molecular beam epitaxy.

In this paper, we use CPGE spectra at inter-band excitation to study the Rashba and Dresselhaus spin splitting in an undoped asymmetric In0.15Ga0.85As/GaAs/AlGaAs step QWs.

Additionally, the presence of a wide and asymmetric enthalpic step, whose position follows Fox predictions, demonstrates miscibility between the blend components.

In the asymmetric key step, which builds up the α-methylpiperidine core 35, the keto diester substrate 36 is converted through an ω-TA-catalyzed transamination reaction into the corresponding amino diester 37 (50 57 g L 1).