(S)-Boc-4-amino-pentanoic acid
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(S)-Boc-4-amino-pentanoic acid

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Category
BOC-Amino Acids
Catalog number
BAT-008793
CAS number
207924-92-3
Molecular Formula
C10H19NO4
Molecular Weight
217.26
(S)-Boc-4-amino-pentanoic acid
IUPAC Name
(4S)-4-[(2-methylpropan-2-yl)oxycarbonylamino]pentanoic acid
Synonyms
(S)-4-((tert-Butoxycarbonyl)amino)pentanoic acid
Appearance
White powder
Purity
≥ 99% (HPLC)
Melting Point
81-102 ºC
InChI
InChI=1S/C10H19NO4/c1-7(5-6-8(12)13)11-9(14)15-10(2,3)4/h7H,5-6H2,1-4H3,(H,11,14)(H,12,13)/t7-/m0/s1
InChI Key
CVYVXURBKURNKE-ZETCQYMHSA-N
Canonical SMILES
CC(CCC(=O)O)NC(=O)OC(C)(C)C
1. Air-stable aryl derivatives of pentafluoroorthotellurate
Daniel Wegener, Kurt F Hoffmann, Alberto Pérez-Bitrián, Ilayda Bayindir, Amiera N Hadi, Anja Wiesner, Sebastian Riedel Chem Commun (Camb). 2022 Aug 25;58(69):9694-9697. doi: 10.1039/d2cc03936b.
We report on two different sets of air-stable derivatives of pentafluoroorthotellurate containing fluorinated and non-fluorinated aryl groups. The acid cis-PhTeF4OH was obtained in gram scale and further transformed to Ag[cis-PhTeF4O], which was used as a cis-PhTeF4O transfer reagent to obtain [PPh4][cis-PhTeF4O]. Furthermore, the synthesis of trans-(C6F5)2TeF3OH was achieved by a selective hydrolysis of trans-(C6F5)2TeF4 in the presence of KF and subsequent protonation by aHF. Quantum-chemical calculations show a higher acidity and robustness against fluoride abstraction for trans-(C6F5)2TeF3OH compared to cis-PhTeF4OH.
2. Natural Products Containing 'Rare' Organophosphorus Functional Groups
Janusz J Petkowski, William Bains, Sara Seager Molecules. 2019 Feb 28;24(5):866. doi: 10.3390/molecules24050866.
Phosphorous-containing molecules are essential constituents of all living cells. While the phosphate functional group is very common in small molecule natural products, nucleic acids, and as chemical modification in protein and peptides, phosphorous can form P⁻N (phosphoramidate), P⁻S (phosphorothioate), and P⁻C (e.g., phosphonate and phosphinate) linkages. While rare, these moieties play critical roles in many processes and in all forms of life. In this review we thoroughly categorize P⁻N, P⁻S, and P⁻C natural organophosphorus compounds. Information on biological source, biological activity, and biosynthesis is included, if known. This review also summarizes the role of phosphorylation on unusual amino acids in proteins (N- and S-phosphorylation) and reviews the natural phosphorothioate (P⁻S) and phosphoramidate (P⁻N) modifications of DNA and nucleotides with an emphasis on their role in the metabolism of the cell. We challenge the commonly held notion that nonphosphate organophosphorus functional groups are an oddity of biochemistry, with no central role in the metabolism of the cell. We postulate that the extent of utilization of some phosphorus groups by life, especially those containing P⁻N bonds, is likely severely underestimated and has been largely overlooked, mainly due to the technological limitations in their detection and analysis.
3. Engineering robust microorganisms for organic acid production
Vinh G Tran, Huimin Zhao J Ind Microbiol Biotechnol. 2022 Apr 14;49(2):kuab067. doi: 10.1093/jimb/kuab067.
Organic acids are an important class of compounds that can be produced by microbial conversion of renewable feedstocks and have huge demands and broad applications in food, chemical, and pharmaceutical industries. An economically viable fermentation process for production of organic acids requires robust microbial cell factories with excellent tolerance to low pH conditions, high concentrations of organic acids, and lignocellulosic inhibitors. In this review, we summarize various strategies to engineer robust microorganisms for organic acid production and highlight their applications in a few recent examples.
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