Anaesthetic quinolines and terpenes and thiophenes

Fmoc-D-threonine.

Fmoc-D-threonine.

Application Tris(diethylamino)phosphine [(Et 2 N) 3 P] can be used as a reagent to synthesize: 1,1&#8242-Dialkylisoindigo derivatives by reacting with various 1-alkylisatins via deoxygenation reaction. 1-Aminomethylisatins by treating with isatin

Application Tris(diethylamino)phosphine [(Et 2 N) 3 P] can be used as a reagent to synthesize: 1,1&#8242-Dialkylisoindigo derivatives by reacting with various 1-alkylisatins via deoxygenation reaction. 1-Aminomethylisatins by treating with isatin

Application Catalyst in: Nickel/Lewis acid-catalyzed aryl- and alkenylcyanation of unsaturated bonds Nickel/Lewis Acid-Catalyzed Cyanoesterification and Cyanocarbamoylation of Alkynes Methoxycarbonylation reactions (palladium complex)

(R)-(-)-Carvone is a monoterpenoid. Its ozonolysis in the gaseous phase has been proposed. Aldehydes (formaldehyde) and biradicals were obtained as the major products. It participates in the diastereoselective synthesis of homochiral

(R)-(-)-Carvone is a monoterpenoid. Its ozonolysis in the gaseous phase has been proposed. Aldehydes (formaldehyde) and biradicals were obtained as the major products. It participates in the diastereoselective synthesis of homochiral

(R)-(-)-Carvone is a monoterpenoid. Its ozonolysis in the gaseous phase has been proposed. Aldehydes (formaldehyde) and biradicals were obtained as the major products. It participates in the diastereoselective synthesis of homochiral

(R)-(-)-Carvone is a monoterpenoid. Its ozonolysis in the gaseous phase has been proposed. Aldehydes (formaldehyde) and biradicals were obtained as the major products. It participates in the diastereoselective synthesis of homochiral

Methyl 3-amino-2-thiophenecarboxylate reacts with hydrazonoyl chlorides in the presence of triethylamine to yield corresponding N-arylamidrazones.Methyl 3-amino-2-thiophenecarboxylate was used in: the synthesis of 4-nitro and 4-aminothienyl

Methyl 3-amino-2-thiophenecarboxylate reacts with hydrazonoyl chlorides in the presence of triethylamine to yield corresponding N-arylamidrazones.Methyl 3-amino-2-thiophenecarboxylate was used in: the synthesis of 4-nitro and 4-aminothienyl

Methyl 3-amino-2-thiophenecarboxylate reacts with hydrazonoyl chlorides in the presence of triethylamine to yield corresponding N-arylamidrazones.Methyl 3-amino-2-thiophenecarboxylate was used in: the synthesis of 4-nitro and 4-aminothienyl