Use of α-phenylglycinol as chiral auxiliary in Strecker synthesis ensures high diastereoselectivity and its easy removal by oxidative cleavage allows large scale preparation of optically active α-amino acids
We report a new methodology for the synthesis of chiral nonproteinaceous alpha-amino acids, which in...
The synthesis of two new diastereomeric 6-amino-3-azabicyclo[3.2.1]octane-6-carboxylic acids exo- an...
Glycosylamines contain the easily cleavable semi-aminal-type N-glycosidic bond. O-Protected glycosyl...
Diastereoselective Strecker reactions based on (R)-phenylglycine amide as chiral auxiliary are repor...
Efficient and stereoselective synthetic routes to enantiomerically pure (2R,3S)- and (2R,3S)-2-amino...
The Strecker amino acid synthesis is a flexible, general strategy for the synthesis of $\alpha$-amin...
α-Amino acids are essential building blocks for protein synthesis, and are also widely useful as com...
A diastereoselective Strecker reaction using (R)-(-)-phenylglycinol forms the basis of a concise sca...
The vicinal amino alcohol is a common motif in natural products and pharmaceuticals. Amino acids con...
none4noThe synthesis of a series of new chiral alpha-aminonitriles was achieved in a diastereoselect...
alpha-Amino acids are doubly benzylated at nitrogen to give N,N-dibenzyl amino adds, which can readi...
threo-\u3b1-Dibenzylamino-beta-hydroxyesters (2) have been synthesised with high diastereoselectivit...
Various optically pure benzocyclobutene and biphenylene-based α-amino acid derivatives are prepared ...
A series of α-quaternary arylglycines were prepared in high optical purity (up to 98% ee) by α-alkyl...
Optically active benzocyclobutene and biphenylene based unusual cc-amino acid derivatives have been ...
We report a new methodology for the synthesis of chiral nonproteinaceous alpha-amino acids, which in...
The synthesis of two new diastereomeric 6-amino-3-azabicyclo[3.2.1]octane-6-carboxylic acids exo- an...
Glycosylamines contain the easily cleavable semi-aminal-type N-glycosidic bond. O-Protected glycosyl...
Diastereoselective Strecker reactions based on (R)-phenylglycine amide as chiral auxiliary are repor...
Efficient and stereoselective synthetic routes to enantiomerically pure (2R,3S)- and (2R,3S)-2-amino...
The Strecker amino acid synthesis is a flexible, general strategy for the synthesis of $\alpha$-amin...
α-Amino acids are essential building blocks for protein synthesis, and are also widely useful as com...
A diastereoselective Strecker reaction using (R)-(-)-phenylglycinol forms the basis of a concise sca...
The vicinal amino alcohol is a common motif in natural products and pharmaceuticals. Amino acids con...
none4noThe synthesis of a series of new chiral alpha-aminonitriles was achieved in a diastereoselect...
alpha-Amino acids are doubly benzylated at nitrogen to give N,N-dibenzyl amino adds, which can readi...
threo-\u3b1-Dibenzylamino-beta-hydroxyesters (2) have been synthesised with high diastereoselectivit...
Various optically pure benzocyclobutene and biphenylene-based α-amino acid derivatives are prepared ...
A series of α-quaternary arylglycines were prepared in high optical purity (up to 98% ee) by α-alkyl...
Optically active benzocyclobutene and biphenylene based unusual cc-amino acid derivatives have been ...
We report a new methodology for the synthesis of chiral nonproteinaceous alpha-amino acids, which in...
The synthesis of two new diastereomeric 6-amino-3-azabicyclo[3.2.1]octane-6-carboxylic acids exo- an...
Glycosylamines contain the easily cleavable semi-aminal-type N-glycosidic bond. O-Protected glycosyl...
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