83537-82-0

Upstream product

• 83537-81-9 (3R,6S)-3-[(benzyloxy)methyl]-6-isopropyl-1,4-dimethoxy-3-methyl-3,6-dihydropyrazine 
• 3587-60-8 Benzyloxymethyl chloride 

Downstream Products

• 145040-36-4 (R)-Boc-O-benzyl-α-methylserine 
• 3398-40-1 (R)-(-)-2-methylserine 
• 134899-85-7 α-methyl serine hydrochloride 
• 176908-57-9 (R)-3-Benzyloxy-2-((2R,3R,4R)-2,4-bis-benzyloxy-3-methyl-pentanoylamino)-2-methyl-propionic acid methyl ester 
• 197567-49-0 (R)-3-Benzyloxy-2-[((2R,4R,5R,6R)-5-hydroxy-5,6-dimethyl-2-phenyl-[1,3]dioxane-4-carbonyl)-amino]-2-methyl-propionic acid methyl ester 
• 197567-55-8 (R)-3-Benzyloxy-2-({(4R,5S)-2,2-dimethyl-5-[(R)-1-(tetrahydro-pyran-2-yloxy)-ethyl]-[1,3]dioxolane-4-carbonyl}-amino)-2-methyl-propionic acid methyl ester 
• 145674-65-3 (S)-Boc-O-benzyl-α-methylserine 
• 176908-55-7 (S)-3-Benzyloxy-2-((2R,3R,4R)-2,4-bis-benzyloxy-3-methyl-pentanoylamino)-2-methyl-propionic acid methyl ester 
• 197567-47-8 (S)-3-Benzyloxy-2-[((2R,4R,5R,6R)-5-hydroxy-5,6-dimethyl-2-phenyl-[1,3]dioxane-4-carbonyl)-amino]-2-methyl-propionic acid methyl ester 
• 197567-54-7 (S)-3-Benzyloxy-2-({(4R,5S)-2,2-dimethyl-5-[(R)-1-(tetrahydro-pyran-2-yloxy)-ethyl]-[1,3]dioxolane-4-carbonyl}-amino)-2-methyl-propionic acid methyl ester 

Relevant academic research and scientific papers

Efficient enantioselective synthesis of orthogonally protected (R)-α-alkylserines compatible with the solid phase peptide synthesis

The Sch?llkopf methodology for the asymmetric synthesis of α-amino acids, which was previously not applicable to the construction of quaternary α-amino acids, has been rendered not only suitable but also practical for this purpose and applied to a highly efficient enantioselective synthesis of orthogonally protected (R)-α-alkylserines suitable for the solid phase synthesis.

ENANTIOSELECTIVE SYNTHESIS OF NON-PROTEINOGENIC AMINO ACIDS VIA METALLATED BIS-LACTIM ETHERS OF 2,5-DIKETOPIPERAZINES

Bis-lactim ethers 1 of 2,5-diketopiperazines contain a chiral inducing center, an acidic CH-bond and two sites susceptible to hydrolysis.They react with BuLi to give Li compounds of type 4, 15, 29 or 32, which possess a prochiral C atom.They readily add electrophiles (such as alkylating agents or carbonyl compounds) with unusually high diastereoface differentiation.In many cases the d.e-value (d.e. = diastereomeric excess = asymmetric induction) of the adduct exceeds 95percent.On hydrolysis the adducts are cleaved liberating the chiral auxiliary (used to build up the bis-lactim ether 1) and the target molecules, the optically active amino acid methyl esters of type 8, 19, 25 or 36.The two amino acid esters are separable either by fractional distillation or (eventually after further hydrolysis to amino acids) by chromatography.Transition state models are discussed that could explain the exceptionally high asymmetric induction and the predictability of the induced configuration.

Asymmetric Syntheses via Heterocyclic Intermediates, XI Enantioselective Synthesis of (R)-(-)-α-Methylserine

Die Titelverbindung 7 wurde in enantiomerenreiner Form durch asymmetrische Synthese dargestellt unter Verwendung des Bislyctimethers 1 von cyclo-(L-Val-DL-Ala) als Ausgangsverbindung.