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Chemical Structure| 70-26-8 Chemical Structure| 70-26-8
Chemical Structure| 70-26-8

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L-ornithine has an antifatigue effect in increasing the efficiency of energy consumption and promoting the excretion of ammonia.

Synonyms: (S)-2,5-Diaminopentanoic acid

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Product Citations

Product Citations

Iram Muzaffar ;

Abstract: Over the years bacteria have developed resistance against antibiotics. Overuse and misuse of antibiotics is one of the main reasons of this increased bacterial resistance. A recently discovered peptide antibiotic known as teixobactin has shown potent activity against Gram-positive bacteria including methicillin-resistant Staphylococcus. aureus (MRSA), Mycobacterium tuberculosis, and vancomycin-resistant enterococci, (VRE). The structure of teixobactin consists of several uncommon amino acids including D-amino-acids and L-allo-enduracididine. L-allo-Enduracididine is a unique amino acid residue consisting of a 5-membered guanidine ring, which offers a great challenge for its synthesis. Most of the reported syntheses of L-allo-enduracididine are lengthy and consist of a lack of stereoselectivity and overall low yields, which stresses the need to develop a more efficient synthetic route to enduracididine using readily available reagents.A synthetic strategy was proposed to construct the 5-membered cyclic guanidine structure using a C-H amination reaction catalyzed by Rh2(esp)2 as the key step. For this purpose, attempts to synthesize various arginine derivatives bearing a 2,2,2-trichloroethoxysulfonyl- (Tces-) protected guanidine were conducted by condensing isothiourea 21 with different derivatives of L-ornithine. First, 2,2,2-trichloroethylsulfamate (24) was synthesized from chlorosulfonyl isocyanate (CSI) with 57% yield. S,S-Dimethyl-N-(2,2,2-trichloroethoxysulfonyl)carbonimidodithionate (25) was made from 24 in 89% yield, which was consequently converted to S-Methyl-N-(2,2,2-trichloroethoxysulfonyl)isothiourea (21) in 94 % yield. Ester derivatives of L-ornithine were synthesized, including N-(δ-tert-butoxycarbonyl)-N-(α-([fluoren-9-yl]methoxy)carbonyl)-L-ornithine methyl ester (28) in 80% yield, and N-(δ-tert-butoxycarbonyl)-N-(α-([fluoren-9-yl]methoxy)carbonyl-L-ornithine allyl ester (34) in 93 % yield. Removal of the Boc protecting group was followed by the attempted coupling of the L-ornithine derivatives with 21, which was unsuccessful and instead gave product whose NMR data was consistent with the formation of a lactam (38) resulting from reaction of the -amino group with the ester. C-H amination was attempted on L-Ornithine, N2-[(9H-fluoren-9-ylmethoxy)carbonyl]-N5-[imino[[(4-methylphenyl)sulfonyl]amino]methyl], methyl ester (41) by using Rh2(esp)2 which gave a complex mixture of compounds. The presented strategy could be used in the future for synthesizing protected arginine derivatives by modifications in the starting molecules. These would serve as substrates for making nitrogen-based heterocyclic compounds via C-H amination by exploring different Rh based catalysts.

Purchased from AmBeed: ; ; ; ; ; 127-19-5

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Product Details of L-Ornithine

CAS No. :70-26-8
Formula : C5H12N2O2
M.W : 132.16
SMILES Code : O=C(O)[C@@H](N)CCCN
Synonyms :
(S)-2,5-Diaminopentanoic acid
MDL No. :MFCD00242584

Safety of L-Ornithine

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of L-Ornithine

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Upstream synthesis route of [ 70-26-8 ]
  • Downstream synthetic route of [ 70-26-8 ]

[ 70-26-8 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 70-26-8 ]
  • [ 143824-77-5 ]
References: [1] Bioorganic and Medicinal Chemistry Letters, 2004, vol. 14, # 4, p. 855 - 857.
 

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