Reduction of Sterically Hindered α,α-disubstituted Amino Esters
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00397919908086041
Reference12 articles.
1. Synthesis of Peptides Containing ?,?-Disubstituted ?-Amino Acids by the Azirine/Oxazolone Method: The (12-20)-Nonapeptide of the Ionophore Alamethicin
2. A New, Stereoselective Reducing Agent
3. A total synthesis of aphidicolin
4. 1-(Arylthio)cyclopropanecarboxaldehydes. Conjunctive reagents for secoalkylation
5. Ate complex from diisobutylaluminum hydride and n-butyllithium as a powerful and selective reducing agent for the reduction of selected organic compounds containing various functional groups
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1. Reevaluating the Substrate Specificity of the L-Type Amino Acid Transporter (LAT1);Journal of Medicinal Chemistry;2018-07-26
2. ChemInform Abstract: Reduction of Sterically Hindered α,α-Disubstituted Amino Esters.;ChemInform;2010-06-15
3. Synthesis and modification of dibenzylglycine derivatives via the Suzuki-Miyaura cross-coupling reaction;Journal of Peptide Research;2004-08
4. Synthesis of highly functionalised dibenzylglycine derivatives via the Suzuki–Miyaura coupling reaction;Bioorganic & Medicinal Chemistry Letters;2002-01
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