CAS: 72150-35-7; (S)-N-(1-Amino-1-Oxo-3-Phenylpropan-2-yl)Benzamide

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CAS号2566-22-5 N-苯甲酰-L-苯丙氨酸

📜Bz-Phe-Ser-Ome置于ruthenium Trichloride,Sodium Periodate体系中,用 四氯化碳,乙腈 作为反应溶剂,化学反应 1.5H,以79%的收率获得产物n-Alpha-苯甲酰基-L-苯丙氨酸酰胺
参考文献:Protein Backbone Modification By Novel C.Alpha.-C Side-Chain Scission
标题:Protein Backbone Modification By Novel C.Alpha.-C Side-Chain Scission
摘要:Alpha-Ketoamide (-Nh-Co-Co-) Units In Intact Peptides Are Generated From Ser/thr Residues Via Ru(Viii)Catalyzed C-Alpha-C Side-Chain Scission. Facets Associated With This Novel Cu-Carbon Modification Have Been Probed With 75 Peptides Chosen To Represent Every Possible Peptide Environment. The Reactions Were Carried Out At Room Temperature With In Situ Generated Ru(Viii) In Biphasic (Ch3Cn/ccl4/ph 3 Phosphate Buffer,1:1:2 V/v) Medium. Whereas Ser/thr Residues Placed At The C-Terminal End In Peptides Undergo N-C Bond Scission Leading To Des-Ser/thr Peptide Amides-Thus Acting As Gly Equivalents In Simulating The Alpha-Amidating Action Of Pituitary Enzymes-Those Located At The N-Terminal Or Nonterminal Or Even At The C-Terminal Position (Protected As Amide) Were Found To Undergo Oxidative C-C Bond Scission (Involving C-Alpha And C Side-Chain Bond),Resulting In The Generation Of Alpha-Ketoamide (-Nh-Co-Co-) Units In The Intact Peptide Backbone. The Difference In The Products Arising From C-Alpha-C Side-Chain Scission Of Ser/thr Esters And Amides Is Rationalized On The Basis Of A Common Mechanism Involving Either Oxaloesters [pep-Nh-Co-Cox; X = Ome] Or Oxalamides [x = Nh2 Or Nh-Pep] Arising From The Oxidation Of Initially Formed Carbinolamide Intermediates [pep-Nh-Ch(Oh)-Cox],Wherein,While The Former Are Shown To Undergo Hydrolysis To Terminal Amides [pep-Nh2],The Oxalamides Are Found To Be Stable To Hydrolysis. Ancillary Noteworthy Findings Are Those Of Peptide Bond Scission When Contiguous Ser-Ser/thr-Thr Residues Are Present And The Oxidative Cleavage At C-Terminal Tyr/trp Sites Generating Des Amides. The Oxidative Methodology Presented Here Is Mild,Simple,And Practical And Proceeds With Chiral Retention. The Insensitivity Of A Large Number Of Amino Acid Residues,Such As Gly,Ala,Leu,Asn,Gln,Asp,Glu,Pro,Arg,Phe,Lys,Val,And Aib,And N-Protecting Groups,Such As B°C,Z,And Bz,Toward Ru(Viii) Under The Experimental Conditions Should Make This Methodology Practical And Useful. Sulfur-Containing Amino Acids Cys And Met Get Oxidized To Sulfones In The Products.
DOI:10.1021/ja00094A008