Results 251 to 260 of about 159,996 (294)

Protease‐Mediated Synthesis of Zein Nanofibrils: From Structural Elucidation to Functional Application

Advanced Science, EarlyView.
The globular shape and hydrophobicity of zein made it unsuitable to be processed in pure aqueous environment. Pepsin‐mediated hydrolysis converts zein into water‐soluble and fibril‐forming peptides with a bioconversion rate exceeding 70%, enabling the self‐assembly of amyloid‐like nanofibrils.
Mingqin Li, Tonghui Jin, Simone Wüthrich, Jiangtao Zhou, Qiyao Sun, Ting Li, Zhou Dong, Eva Maria Zunzuneigui Bru, Raffaele Mezzenga   +8 more
wiley   +1 more source

gem-Difluorovinyl and trifluorovinyl Michael acceptors in the synthesis of α,β-unsaturated fluorinated and nonfluorinated amides. [PDF]

Beilstein J Org Chem
Bilska-Markowska M, Kaźmierczak M, Jankowski W, Hoffmann M.   +3 more
europepmc   +1 more source

Quantification of the effects of n-π* interactions on the H-bonding properties of amide groups. [PDF]

Chem Sci
Hanna FE, Bond AD, Hunter CA.
europepmc   +1 more source

Regioselective formal hydrocyanation of allenes: synthesis of β,γ-unsaturated nitriles with α-all-carbon quaternary centers. [PDF]

Beilstein J Org Chem
Lim S, Kim T, Lee Y.
europepmc   +1 more source

2D Interfacial Crystallization Stabilized by Short-Chain Aliphatic Interfaces. [PDF]

Langmuir
Swanson HWA, Barriales K, Sherman EA, Li TD, Kennedy AR, Tuttle T, Ulijn RV, Lau KHA.   +7 more
europepmc   +1 more source

Novel 3-Aminothieno[2,3-b]pyridine-2-carboxamides with Activity against Mycobacterium tuberculosis. [PDF]

ACS Med Chem Lett
Lynde BE, Chemaly DM, Baldin VP, Greve E, Harding CL, Graner JM, Hardy M, Chowdhury S, Parish T.   +8 more
europepmc   +1 more source

Identification of novel amides and alkaloids as putative inhibitors of dopamine transporter for schizophrenia using computer-aided virtual screening. [PDF]

Front Pharmacol
Ahmad I, Tassawer A, Khan MU, Shehroz M, Nishan U, Sheheryar S, Dib H, Abdelfattah MAO, Shah M.   +8 more
europepmc   +1 more source

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Amide–Amide Hydrogen Bonding. Semirubin Amides

Monatshefte für Chemie - Chemical Monthly, 2006
Semirubins are analogs for one-half of the bilirubin structure and capable of intramolecular hydrogen bonding. Semirubin amides of ammonia and primary amines are also capable of intramolecular hydrogen bonding. From a combination of spectroscopic methods (1H NMR, NOE, and VPO), the primary amide is found to engage very effectively in intramolecular ...
Nicholas T. Salzameda, David A. Lightner
openaire   +2 more sources

Amides

ChemInform, 2005
AbstractFor Abstract see ChemInform Abstract in Full Text.
Patrick D. Bailey, Richard A. Price, Rachel Pettecrew, Timothy J. Mills   +3 more
openaire   +2 more sources

Flexible and Chemoselective Oxidation of Amides to α-Keto Amides and α-Hydroxy Amides [PDF]

Journal of the American Chemical Society, 2017
A suite of flexible and chemoselective methods for the transition-metal-free oxidation of amides to α-keto amides and α-hydroxy amides is presented. These highly valuable motifs are accessed in good to excellent yields and stereoselectivities with high functional group tolerance.
Aurélien de la Torre, Daniel Kaiser, Nuno Maulide   +2 more
openaire   +3 more sources