One-Pot Substitution Approach for the Syntheses of Nonfunctional and Functional Poly[(amino acid ester)phosphazene] Biomaterials

2016 ◽  
Vol 302 (2) ◽  
pp. 1600318 ◽  
Author(s):  
Amanda L. Baillargeon ◽  
Kalin I. Penev ◽  
Kibret Mequanint
2019 ◽  
Vol 43 (3-4) ◽  
pp. 90-96
Author(s):  
Yongjian Zhang ◽  
Junyi Su ◽  
Tengfei Lin ◽  
Zhangqi Lin ◽  
Zichun Zhou ◽  
...  

A series of more than 20 multisubstituted pyrrolidine-2-carboxylates were synthesized via a one-pot cycloaddition of an araldehyde, an amino acid ester, and a chalcone catalyzed by I2/K2CO3 in tetrahydrofuran at 80 °C. The advantages of this method are readily available starting materials, mild conditions, and simple operation, and it is metal free and yields are good to excellent.


ChemInform ◽  
2010 ◽  
Vol 28 (44) ◽  
pp. no-no
Author(s):  
M. L. BOYS ◽  
K. J. CAIN-JANICKI ◽  
W. W. DOUBLEDAY ◽  
P. N. FARID ◽  
M. KAR ◽  
...  

1997 ◽  
Vol 1 (3) ◽  
pp. 233-239 ◽  
Author(s):  
Mark L. Boys ◽  
Kimberly J. Cain-Janicki ◽  
Wendel W. Doubleday ◽  
Payman N. Farid ◽  
Mangalya Kar ◽  
...  

2015 ◽  
Vol 51 (39) ◽  
pp. 8373-8376 ◽  
Author(s):  
Zhangjun Huang ◽  
Shuangshuang Chen ◽  
Xuemin Lu ◽  
Qinghua Lu

Water-triggered self-assembly polycondensation was proposed for preparation of cyclomatrix polyphosphazene nanoparticles from amino acid ester, and a critical solubility parameter was found to determine whether the nanoparticles were formed.


Synlett ◽  
2018 ◽  
Vol 29 (14) ◽  
pp. 1921-1925 ◽  
Author(s):  
Song Bai ◽  
Shan Liu ◽  
Yunying Zhu ◽  
Kunhong Zhao ◽  
Qin Wu

A series of both enantiomers of chiral β-amino acid ester derivatives containing a 4-(piperidin-1-yl)pyrimidine moiety was prepared in high yield and excellent enantioselectivity excess (up to >99% enantiomeric excess) using a chiral cinchona alkaloid thiourea catalyst under one-pot solvent-free conditions. Antiviral bioassay experimental results showed that some of the chiral products exhibited higher antiviral activities against tobacco mosaic virus (TMV) in vivo than the commercial antiviral agent ningnanmycin.


2020 ◽  
Vol 27 ◽  
Author(s):  
Santosh Y. Khatavi ◽  
K. Kantharaju

Background: Agro-waste derived solvent media act as a greener process for the peptide bond formation using Nα - Fmoc-amino acid chloride and amino acid ester salt with in situ neutralization and coupling under biphasic condition. The Fmoc-amino acid chlorides are prepared by the reported procedure of freshly distilled SOCl2 with dry CH2Cl2. The protocol found many added advantages such as neutralization of amino acid ester salt and not required additional base for the neutralization, and directly coupling take place with Fmoc-amino acid chloride gave final product dipeptide ester in good to excellent yields. The protocol occurs with complete stereo chemical integrity of the configuration of substrates. Here, we revisited Schotten-Baumann condition, instead of using inorganic base. Objective: To develop green protocol for the synthesis of peptide bond using Fmoc-amino acid chloride with amino acid esters salt. Methods: The final product isolated is analyzed in several spectroscopic and analytical techniques such as FT-IR, 1H-, 13CNMR, Mass spectrometry and RP-HPLC to check stereo integrity and purity of the product. Conclusion: The present method developed greener using natural agro-waste (lemon fruit shell ash) derived solvent medium for the reaction and not required chemical entity.


2020 ◽  
Vol 85 (2) ◽  
pp. 464-466
Author(s):  
Kenzo Yokozeki ◽  
Isao Abe

ABSTRACT Here, we report a novel industrial aspartame production route, involving the enzymatic production of α-l-aspartyl-l-phenylalanine β-methylester from l-aspartic acid dimethylester and l-phenylalanine by α-amino acid ester acyl transferase. The route also involves the chemical transformation of α-l-aspartyl-l-phenylalanine β-methylester to α-l-aspartyl-l-phenylalanine methylester hydrochloride (aspartame hydrochloride) in an aqueous solution with methanol and HCl, followed by HCl removal to form aspartame.


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