Results 131 to 140 of about 667,303 (272)

General phase diagram for antiferroelectric liquid crystals in dependence on enantiomeric excess [PDF]

, 2002
Ewa Górecka, Damian Pociecha, Mojca Čepič, B. Žekš, R. Dąbrowski   +4 more
openalex   +1 more source

Amplification of Enantiomeric Excess in a Proline‐Mediated Reaction [PDF]

Angewandte Chemie International Edition, 2004
Suju P, Mathew, Hiroshi, Iwamura, Donna G, Blackmond   +2 more
openaire   +2 more sources

A Plant‐Based Platform for the Production of Bark Beetle Pheromones

Plant Biotechnology Journal, EarlyView.
ABSTRACT Bark beetle species of the genera Ips and Dendroctonus represent a threat to forests in both North America and Europe. Under normal circumstances, these beetles recycle dying trees into nutrients, but under certain conditions, growing populations can overcome healthy tree defenses and cause severe economic loss in forestry.
Abraham Ontiveros‐Cisneros, Jule Salfeld, Sofia Paulsson, Bao‐Jian Ding, Hong‐Lei Wang, Magne Friberg, Christer Löfstedt, Olivier Van Aken   +7 more
wiley   +1 more source

At-line determination of the enantiomeric excess in multi-component chiral samples using Raman Optical Activity (ROA) [PDF]

Karolina Kwiecień, Piotr Putyra, Agnieszka Kaczor   +2 more
openalex   +1 more source

Magnetic Circular Dichroism in Archean Stratospheric Oxygen: Enantiomeric Excess of Amino Acids Produced in Volcanic Plumes [PDF]

, 2023
Anuj K. Sharma
openalex   +1 more source

Molecular basis and biological relevance of bacterial and plant pinoresinol/lariciresinol reductase specificities

Protein Science, Volume 35, Issue 2, February 2026.
Abstract A bacterial pinoresinol/lariciresinol reductase (PLR) homolog named NrPinZ was obtained from a Novosphingobium rhizosphaerae sp. LY bacterial strain, with NrPinZ being part of its 5‐step biochemical system catabolizing pinoresinol into coniferyl aldehyde and vanillin.
Clyde A. Smith, Diana L. Bedgar, Michael A. Costa, Syed G. A. Moinuddin, Marco N. Allemann, Joshua K. Michener, Laurence B. Davin, Norman G. Lewis   +7 more
wiley   +1 more source

A non-chiral lithium aluminate reagent for the determination of enantiomeric excess of chiral alcohols

, 2016
Raúl García‐Rodríguez, Schirin Hanf, Andrew D. Bond, Dominic S. Wright   +3 more
openalex   +2 more sources

Determining the Enantiomeric Excess and Absolute Configuration\nof <i>In Situ</i> Fluorine-Labeled Amines and Alcohols by ¹⁹F NMR Spectroscopy

, 2021
Sumin Jang (5932508), Hahyoun Park (11874559), Quynh Huong Duong (11874562), Eun-Jeong Kwahk (11478909), Hyunwoo Kim (690467)   +4 more
openalex   +2 more sources

Asymmetric Catalytic Hydrogenation toward a Value‐Added Chiral Building Block: Optically Active γ‐Butyrolactone Scaffold from Renewable and Synthetic Derived Feedstocks

European Journal of Organic Chemistry, Volume 29, Issue 3, January 22, 2026.
This brief compendium summarizes the most successful asymmetric hydrogenation strategies for the preparation of chiral monocyclic γ‐lactone derivatives from keto acids and keto esters, with emphasis on their relevance for large‐scale production and high enatioselectivities. This article provides a brief compendium on the production of chiral monocyclic
Marta Feliz, Maria J. Sabater
wiley   +1 more source

The asymmetric synthesis of (+)-sitophilure, the natural form of the aggregation pheromone of Sitophilus oryzae L. and Sitophilus zeamais M.

Journal of the Brazilian Chemical Society, 1999
The asymmetric synthesis of (+)-sitophilure, the aggregation pheromone of Sitophilus oryzae L. and Sitophilus zeamais M., was carried out in 12 steps, 18% overall yield and 82% enantiomeric excess from the enzymatic reduction of methyl 3-oxopentanoate ...
Pilli Ronaldo A., Riatto Valéria B.
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