scholarly journals Biosynthetic reconstitution of deoxysugar phosphoramidate metalloprotease inhibitors using an N–P-bond-forming kinase

2019 ◽  
Vol 10 (16) ◽  
pp. 4486-4490 ◽  
Author(s):  
Alexandra Baulig ◽  
Irina Helmle ◽  
Marius Bader ◽  
Felix Wolf ◽  
Andreas Kulik ◽  
...  
Keyword(s):  
Amino Acids ◽  
Bond Forming ◽  
Metalloprotease Inhibitors

In the biosynthesis of phosphoramidon-like metalloprotease inhibitors three enzymes cooperate in the condensation of two amino acids and the subsequent attachment of a 6-deoxyhexose via a phosporamidate bridge.

scholarly journals Organometallic AlaM Reagents for Umpolung Peptide Diversification

2021 ◽  
Author(s):  
Feng Zhu ◽  
Wyatt Powell ◽  
Ruiheng Jing ◽  
Maciej Walczak
Keyword(s):  
Amino Acids ◽  
Open Access ◽  
Cyclic Peptides ◽  
Room Temperature ◽  
Medium Size ◽  
Bond Forming ◽  
Promising Strategy ◽  
Structure Activity ◽  
New Type ◽  
Absolute Control

Selective modification of peptides and proteins is emerging as a promising strategy to develop novel mechanistic probes and prepare compounds with translational potential. While many methods to perform direct bioconjugation rely on reactions with dehydroalanine, an alternative strategy capitalizing on polarity reversal at the β carbon in amino acids can open access to a new type of diversification reactions characterized by absolute control of regio- and stereoselectivity. Here, we report that alanine carbastannatranes Ala<sup>Sn</sup> can serve as a universal synthon in various C-C and C-heteroatom bond-forming reactions demonstrated in over 50 diverse examples. These reagents are compatible with peptide and protein manipulation techniques and undergo chemoselective conjugation in minutes when promoted by Pd(0). Despite their increased nucleophilicity and propensity to transfer the alkyl group, Ala<sup>Sn</sup> operate at room temperature under buffered conditions (pH 6.5-8.5). We also show that Ala<sup>Sn</sup> can be easily transformed into several canonical L- and D-amino acids in arylation, acylation, and etherification reactions. Furthermore, Ala<sup>Sn</sup> can partake in macrocyclizations exemplified by the synthesis of medium size cyclic peptides with various topologies (7-13 membered macrocycles). Taken together, metalated alanine Ala<sup>Sn</sup> demonstrate unparalleled scope and represent a new type of umpolung reagents suitable for structure-activity relationship studies and peptide diversification.

Synthesis of Unnatural Amino Acids via Reductive C-C Bond Forming Hydrogenation

Synfacts ◽  
2005 ◽  
Vol 2006 (01) ◽  
pp. 0049-0049
Author(s):  
M. Krische ◽  
J.-R. Kong ◽  
C.-W. Cho
Keyword(s):  
Amino Acids ◽  
Unnatural Amino Acids ◽  
Bond Forming

Organometallic AlaM Reagents for Umpolung Peptide Diversification

2021 ◽  
Author(s):  
Feng Zhu ◽  
Wyatt Powell ◽  
Ruiheng Jing ◽  
Maciej Walczak
Keyword(s):  
Amino Acids ◽  
Open Access ◽  
Cyclic Peptides ◽  
Room Temperature ◽  
Medium Size ◽  
Bond Forming ◽  
Promising Strategy ◽  
Structure Activity ◽  
New Type ◽  
Absolute Control

Selective modification of peptides and proteins is emerging as a promising strategy to develop novel mechanistic probes and prepare compounds with translational potential. While many methods to perform direct bioconjugation rely on reactions with dehydroalanine, an alternative strategy capitalizing on polarity reversal at the β carbon in amino acids can open access to a new type of diversification reactions characterized by absolute control of regio- and stereoselectivity. Here, we report that alanine carbastannatranes Ala<sup>Sn</sup> can serve as a universal synthon in various C-C and C-heteroatom bond-forming reactions demonstrated in over 50 diverse examples. These reagents are compatible with peptide and protein manipulation techniques and undergo chemoselective conjugation in minutes when promoted by Pd(0). Despite their increased nucleophilicity and propensity to transfer the alkyl group, Ala<sup>Sn</sup> operate at room temperature under buffered conditions (pH 6.5-8.5). We also show that Ala<sup>Sn</sup> can be easily transformed into several canonical L- and D-amino acids in arylation, acylation, and etherification reactions. Furthermore, Ala<sup>Sn</sup> can partake in macrocyclizations exemplified by the synthesis of medium size cyclic peptides with various topologies (7-13 membered macrocycles). Taken together, metalated alanine Ala<sup>Sn</sup> demonstrate unparalleled scope and represent a new type of umpolung reagents suitable for structure-activity relationship studies and peptide diversification.

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