Hypnotic pyrrolidines

Benzyl 3-pyrroline-1-carboxylate, also known as N-benzyloxycarbonyl 3-pyrroline, is an N-substituted 3-pyrroline. Its enthalpy of vaporization at boiling point has been evaluated.[5] Its epoxidation using m-chloroperbenzoic acid (m-CPBA) has been

Benzyl 3-pyrroline-1-carboxylate, also known as N-benzyloxycarbonyl 3-pyrroline, is an N-substituted 3-pyrroline. Its enthalpy of vaporization at boiling point has been evaluated.[5] Its epoxidation using m-chloroperbenzoic acid (m-CPBA) has been

Benzyl 3-pyrroline-1-carboxylate, also known as N-benzyloxycarbonyl 3-pyrroline, is an N-substituted 3-pyrroline. Its enthalpy of vaporization at boiling point has been evaluated.[5] Its epoxidation using m-chloroperbenzoic acid (m-CPBA) has been

Benzyl 3-pyrroline-1-carboxylate, also known as N-benzyloxycarbonyl 3-pyrroline, is an N-substituted 3-pyrroline. Its enthalpy of vaporization at boiling point has been evaluated.[5] Its epoxidation using m-chloroperbenzoic acid (m-CPBA) has been

Product description：Diethyl 3,4-pyrroledicarboxylate (Diethyl 1H-pyrrole-3,4-dicarboxylate) is a 3,4-pyrrole dicarboxylic diester. It has been prepared by the hydrolysis of diethyl 1-benzoyl-3,4-pyrroledicarboxylate and confirmed by IR, NMR and mass

Product description：Diethyl 3,4-pyrroledicarboxylate (Diethyl 1H-pyrrole-3,4-dicarboxylate) is a 3,4-pyrrole dicarboxylic diester. It has been prepared by the hydrolysis of diethyl 1-benzoyl-3,4-pyrroledicarboxylate and confirmed by IR, NMR and mass

Product description：Diethyl 3,4-pyrroledicarboxylate (Diethyl 1H-pyrrole-3,4-dicarboxylate) is a 3,4-pyrrole dicarboxylic diester. It has been prepared by the hydrolysis of diethyl 1-benzoyl-3,4-pyrroledicarboxylate and confirmed by IR, NMR and mass

Product description：Diethyl 3,4-pyrroledicarboxylate (Diethyl 1H-pyrrole-3,4-dicarboxylate) is a 3,4-pyrrole dicarboxylic diester. It has been prepared by the hydrolysis of diethyl 1-benzoyl-3,4-pyrroledicarboxylate and confirmed by IR, NMR and mass

DJS

Application：Reactant for:Synthesis of trisubstituted pyrroles via rearrangement reactions catalyzed by Ir catalystPreparation of biologically active molecules.

Application Pyridyne precursor can be activated under mild fluoride conditions which are highly reactive with dienes and other dipolariphiles (e.g.

This is a Buchwald third generation precatalyst that can be used in:1.Direct ortho-arylation of pyridinecarboxylic acids.2.Catalyzing Suzuki–Miyaura cross-coupling in the synthesis of 1-heteroaryl-3-azabicyclo[3.1.0]hexanes.3.Palladium-catalyzed