Results 181 to 190 of about 10,824 (225)
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1,2,3‐Oxadiazoles

ChemInform, 2005
AbstractFor Abstract see ChemInform Abstract in Full Text.
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A Preferred Synthesis of 1,2,4‐Oxadiazoles

Synthetic Communications, 2004
AbstractFor Abstract see ChemInform Abstract in Full Text.
Brenda Pipik   +3 more
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Oxadiazole grafts in peptide macrocycles

Nature Chemistry, 2016
Synthetic methods that provide control over macrocycle conformation and, at the same time, mitigate the polarity of peptide bonds represent valuable tools for the discovery of new bioactive molecules. Here, we report a macrocyclization reaction between a linear peptide, an aldehyde and (N-isocyanimino)triphenylphosphorane.
John R, Frost   +2 more
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Poly‐1,3,4‐oxadiazoles. III. Alicyclic poly‐1,3,4‐oxadiazoles

Die Makromolekulare Chemie, 1966
AbstractSome alicyclic poly‐1,3,4‐oxadiazoles were prepared from cycloalkanedicarboxylic dihydrazides or from cycloalkanedicarboxylic acids and hydrazine sulfate by solution polycondensation in polyphosphoric acid. These polymers were characterized by high melting temperature.
Yoshio Iwakura   +2 more
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1,2,5-Oxadiazole

2015
[288-37-9] C2H2N2O (MW = 70.050) InChI = 1S/C2H2N2O/c1-2-4-5-3-1/h1-2H InChIKey = JKFAIQOWCVVSKC-UHFFFAOYSA-N (small-molecule heterocyclic pharmacophore) Physical Data: bp 98 °C, mp −28 °C. Alternate Name: furazan. Handling: compound known to possess potent biological activities in humans; toxic by skin contact or ...
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1,2,3-Oxadiazole

2015
[288-43-7] C2H2N2O (MW 70.06) InChI = 1S/C2H2N2O/c1-2-5-4-3-1/h1-2H InChIKey = WCPAKWJPBJAGKN-UHFFFAOYSA-N (1,5-electrocyclic ring opening3; 1,3-dipolar cycloaddition7 with alkynes and nitrous oxide)
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1,3,4‐Oxadiazoles

ChemInform, 2005
AbstractFor Abstract see ChemInform Abstract in Full Text.
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Mass spectrometric analysis of 1,2,4‐Oxadiazoles and 4,5‐Dihydro‐1,2,4‐Oxadiazoles

Mass Spectrometry Reviews, 2004
Abstract1,2,4‐Oxadiazoles and 4,5‐dihydro‐1,2,4‐oxadiazoles are an interesting class of compounds because of their pharmacological and other properties. Although short descriptions of these compounds under mass spectrometric conditions exist, we thought it worthwhile to write a comprehensive review of this class of compounds.
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Saccharide oxadiazoles

Carbohydrate Research, 1975
M A, Shaban   +3 more
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