Results 61 to 70 of about 913 (183)

New Horizon and Advancements in Synthetic and Biological Applications of Active Methylene Acetonitrile: Mini-Review

open access: yesJournal of Chemistry
Acetonitrile is generally used as an organic solvent and can also be used as a significant starting material via active methylene acetonitrile in organic synthesis.
Lavanya Nagamalla   +4 more
doaj   +1 more source

Preparation of 3,4,5-Trisubstituted Oxazolones by Pd-Catalyzed Coupling of N‑Alkynyl tert-Butyloxycarbamates with Aryl Halides and Related Electrophiles

open access: yes, 2016
A novel palladium-catalyzed approach for the assembly of 3,4,5-trisubstituted oxazolones has been achieved by the coupling of N-alkynyl tert-butyloxycarbamates with aryl halides and related electrophiles, which involves an oxidative addition followed by ...
Gangguo Zhu (1508137)   +5 more
core   +3 more sources

The use of 4-hetarylidene- and 4-arylidene-5(4H)-oxazolones as dienophiles. Appropriate reagents to synthesize cyclic analogues of natural amino acids

open access: yes, 1997
This report describes the behavior of 4-hetaryliden- and 4-aryliden-5(4H)-oxazolones as dienophiles in the Diels-Alder reaction with several dienes.
Peregrina, J.M. [0000-0003-3778-7065]   +4 more
core   +1 more source

Stereoselective, Ruthenium-Photocatalyzed Synthesis of 1,2-Diaminotruxinic Bis-amino Acids from 4Arylidene-5(4H)oxazolones

open access: yes, 2022
The irradiation of (Z)-2-phenyl-4-aryliden-5­(4H)-oxazolones 1 in deoxygenated CH2Cl2 at 25 °C with blue light (465 nm) in the presence of [Ru­(bpy)3]­(BF4)2 (5% mole ratio) as a triplet photocatalyst promotes the [2+2] photocycloaddition of the CC bonds
Cristian Silvestru   +19 more
core   +1 more source

Synthesis of 5(4H)-oxazolones from cysteine

open access: yes, 2018
5(4H)-Oksazolona iegūšana no cisteīna. Štrāla S., zinātniskais vadītājs Dr. ķīm., doc. Kļimenkovs I. Kursa darbs organiskajā ķīmijā, 39 lappuses, 10 attēli, 5 tabulas, 32 literatūras avoti, 4 pielikumi. Latviešu valodā.
Štrāla, Signija
core  

A Theoretical (AM1) and Experimental Dipole Moment Study of 5(4H)-Oxazolones

open access: yes, 1992
Experimental and calculated (AM1) dipole moments have been determined for a series of Z and E-isomers of 4-phenylmethylene-5(4H)-oxazolones (1) and 4(a-phenylethylidene)-5(4H)- oxazolones (2) in order to study the conformation in solution of the phenyl ...
C. Cativiela   +11 more
core   +1 more source

Merocyanines Derived from Oxazolone

open access: yes, 1970
Merocyanines, derived from different 2-aryl oxazolone as the acidic nuclei and various basic nuclei like 2-methyl 4-phenyl thiazola, 2-methyl benzothiazole, quinoline-2, quinoline-4 and alpha-picoline have been studied with a view to examining the effect of different substituents present at the position-2 of the oxazolone nucleus on the absorption and ...
E. Jena, P. B. Tripathy
openaire   +1 more source

Reactive Intermediates in Peptide Synthesis:  First Crystal Structures and ab Initio Calculations of 2-Alkoxy-5(4H)-oxazolones from Urethane-Protected Amino Acids

open access: yes, 2016
The structures of the 2-alkoxy-5(4H)-oxazolones derived from 2,2,6,6-tetramethyl-4-[(benzyloxycarbonyl)amino]-1-oxypiperidine-4-carboxylic acid and 2,2,6,6-tetramethyl-4-[(9‘-fluorenylmethoxycarbonyl)amino]-1-oxypiperidine-4-carboxylic acid have been ...
Marco Crisma (1522954)   +4 more
core   +2 more sources

Synthesis of oxazolones from aminoacids containing hydroxyl groups

open access: yes, 2018
Oksazolonu iegūšana no hidroksilgrupu saturošām aminoskābēm. Kokars D., zinātniskais vadītājs doc. Igors Kļimenkovs. Bakalaura darbs, 51 lapaspuse, 13 attēli, 1 tabulas, 17 literatūras avoti, 15 pielikumi. Latviešu valodā.
Kokars, Dāvis
core  

Synthesis of New 5-Oxazolones: Their Ring Opening Reactions to Obtain New Benzamide Derivatives

open access: yes, 2017
New 5-oxazolones have been synthesized via N-protected amino acids which were prepared from various aryl acyl halides and L-amino acids, with DCC. Then, we studied the ring opening reactions of 5-oxazolones with nucleophilic attack by primary aryl amines
Kaya, Kerem   +4 more
core   +1 more source

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