Chapter 10 Synthesis of aprepitant
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Elsevier
Reference22 articles.
1. Structural Optimization Affording 2-(R)-(1-(R)-3,5-Bis(trifluoromethyl)phenylethoxy)-3-(S)-(4-fluoro)phenyl-4- (3-oxo-1,2,4-triazol-5-yl)methylmorpholine, a Potent, Orally Active, Long-Acting Morpholine Acetal Human NK-1 Receptor Antagonist
2. The asymmetric synthesis of .alpha.-amino acids. Electrophilic azidation of chiral imide enolates, a practical approach to the synthesis of (R)- and (S)-.alpha.-azido carboxylic acids
3. The highly stereospecific enzyme catalysed transamination of 4-fluorophenylglyoxylic acid to 4-(S)-fluorophenylglycine
4. A Facile Synthesis of Substituted Phenylglycines
5. Crystallisation induced resolution of 4-fluorophenylglycine
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1. Zinc chloride-catalyzed cyclizative 1,2-rearrangement enables facile access to morpholinones bearing aza-quaternary carbons;Communications Chemistry;2023-10-07
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3. New Developments in Chiral Phosphoric Acid Catalysis for Amine Synthesis;Current Organic Chemistry;2022-05
4. Catalytic Enantioselective Synthesis of Morpholinones Enabled by Aza-Benzilic Ester Rearrangement;Journal of the American Chemical Society;2021-05-06
5. Stereoselective Synthesis of syn-γ-Hydroxynorvaline and Related α-Amino Acids;Synthesis;2019-10-16
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