SYNTHESIS OF α-AMINO-β-HYDROXY-n-BUTYRIC ACIDS
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چکیده
منابع مشابه
SYNTHESIS OF a-AMINO-p-HYDROXY-n-BUTYRIC ACIDS VII. AN IMPROVED SYNTHESIS OF DL-ALLOTHREONINE
Several methods are available for the synthesis of DL-threonine (l-3). However, each of these involves the separation of threonine from a mixture containing varying proportions of the isomeric allothreonine. Recently it has been reported that derivatives of rm-allothreonine may be converted to DL-threonine in excellent yields (3-5). These developments make the preparation of nn-allothreonine of...
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A straightforward metal-free synthesis of anti-β-hydroxy-r-amino acids is described. The organic base-mediated decarboxylative aldol reaction of cheap, readily available r-amidohemimalonates with various aldehydes afforded under very mild conditions anti-β-hydroxy-r-amido esters in high yields and complete diastereoselectivity. Simple one-pot subsequent transformations enabled the corresponding...
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The stereoselective synthesis of β -amino acids and their derivatives has been an active area of research, due to the importance of β -amino acids in various fields [1]. In particular, non-proteinogenic β -amino α-hydroxy acids are found in many natural products and drugs, for example N-benzoyl-3-phenylisoserine as a side-chain of taxol which has been approved for treatment of ovarian and breas...
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Synthesis of Nand O-acyl derivatives of dl-serine and threo-dl-phenylserine was accomplished by a regioselective acylation of the corresponding amino acid. The residues introduced into amino acid structure contain hydrophobic long chain or aromatic, namely lauroyl, myristoyl and phenylacetyl moieties. The fungicidal activity against six strains of fungi was studied. Several compounds were found...
متن کاملDevelopment of ProPhenol Ligands for the Diastereo- and Enantioselective Synthesis of β-Hydroxy-α-amino Esters
A zinc-ProPhenol-catalyzed direct asymmetric aldol reaction between glycine Schiff bases and aldehydes is reported. The design and synthesis of new ProPhenol ligands bearing 2,5-trans-disubstituted pyrrolidines was essential for the success of this process. The transformation operates at room temperature and affords syn β-hydroxy-α-amino esters in high yields with good to excellent levels of di...
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ژورنال
عنوان ژورنال: Journal of Biological Chemistry
سال: 1937
ISSN: 0021-9258
DOI: 10.1016/s0021-9258(18)74436-0