725743-41-9Relevant academic research and scientific papers
HETEROCYCLIC GLP-1 AGONISTS
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Page/Page column 177-178; 114-115, (2021/11/06)
This disclosure relates to GLP-1 agonists of Formula (I): including pharmaceutically acceptable salts and solvates thereof, and pharmaceutical compositions including the same.
Synthetic method of pibrentasvir intermediate
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Paragraph 0036-0039, (2019/04/30)
The invention relates to the technical field of organic synthesis, in particular to a synthetic method of a pibrentasvir intermediate. The synthetic method comprises the steps that S1, a compound IV and a bromination reagent are subjected to a bromination
COMPOSITIONS AND METHODS FOR CONTROL OF DISEASE
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Paragraph 0311; 0319, (2018/08/30)
Compounds, compositions and methods for controlling root-originating diseases are described herein. The compounds include oxazoles, oxadiazoles and thiadiazoles. The compounds may be administered to plants, seeds, and/or soil.
COMPOSITIONS AND METHODS FOR IMPROVING AGRONOMIC CHARACTERISTICS OF PLANTS
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Paragraph 0399, (2016/07/05)
Compounds, compositions and methods for improving one or more agronomic characteristics of desired crop plants are described herein. The compounds include oxazoles, oxadiazoles and thiadiazoles.
Compostions and Methods for Controlling Nematodes
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Page/Page column 39, (2009/03/07)
Compositions and processes for controlling nematodes are described herein, e.g., nematodes that infest plants or animals. The compounds include oxazoles, oxadiazoles and thiadiazoles.
Process for producing optically active carbinols
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, (2008/06/13)
The present invention relates to a process for producing optically active halomethyl phenyl carbinols of the formula (1), comprising reducing halomethyl phenyl ketones of the formula (2) using an asymmetric reducing agent obtained from boranes and optically active α-phenyl-substituted-β-amino alcohols of the formula (3) or optically active α-non-substituted-β-amino alcohols of the formula (4). The present invention further relates to a process for producing optically active carbinols, comprising reacting a prochiral keytone with an asymmetric reducing agent obtained from optically active β-amino alcohols of the formula (5), a metal boron hydride and Lewis acid or lower dialkyl sulfuric acid. All of the formulas (1) to (5) are the same as shown in the specification.
