Abstract:
PURPOSE: A novel catalyst for intermolecular hydroamination and a method for manufacturing cyclic imine compounds using the catalyst are provided to produce the novel catalyst by using an amino Alkynes derivative. CONSTITUTION: A novel catalyst for intermolecular hydroamination uses a catalyst composition including a titanium-amino metal compound, a 4B family metal complex, a 4B family metal compound and specified ligand. The catalyst for intermolecular hydroamination is a titanium - amino compound indicated as a chemical formula 2. The chemical formula 2 is TiClp(NR2)q. R is a straight-chain or a branched-chain alkyl group of C1~C6. P is 0 or 1 and p+q=4. The catalyst is the 4B family metal complex indicated by a chemical formula 3a, 3b or 3c. X and Q is one of the straight-chain or a branched-chain alkyl group of C1~C6, a phenyl radical or a benzyl radical. M is 4B family metal atoms.
Abstract:
A dihydrofuran derivative is provided to improve yield of the dihydrofuran derivative through intramolecular cyclization of alenyl alcohol compound and use as a precursor in synthesis of medicine or perfume. A dihydrofuran derivative is denoted by the chemical formula 1. In the chemical formula 1, R is independently (C1-C7) alkyl group, A is hydrogen, (C1-C7)alkyl, (C3-C8)cycloalkyl, (C6-C20)aryl or (C6-C20)aryl(C1-C7)alkyl. The dihydrofuran derivative is a compound of the chemical formula 2 or 3. The dihydrofuran derivative of the chemical formula 1 is produced through intramolecular cyclization of homoalenyl alcohol compound.
Abstract:
A allenyn-1,6-diol derivative, and a method for preparing the derivative are provided to obtain a source material useful as a source material for the intermolecular cyclization using a transition metal catalyst. An allenyn-1,6-diol derivative is represented by the formula 1, wherein A and B are H, a C1-C6 alkyl group, a C5-C8 cycloalkyl group, a phenyl group substituted or unsubstituted with a halogen atom, a nitro group, a C1-C6 alkyl group, a C1-C6 alkoxy group, a C2-C6 alkylcarbonyl group, a C2-C6 alkoxycarbonyl group or a C2-C6 alkanoate group, a phenyl-C1-C6 alkyl group, a phenyl-C2-C6 alkenyl group, or a 5 to 8-membered heterocyclic group containing an oxygen atom, but A and B cannot be H simultaneously.
Abstract:
A method for coupling carbon atoms in an unsaturated hydrocarbon compound molecule by using organoindium is provided to avoid an additional purification step for separating an intermediate compound produced by a transition metal catalyst and indium, to solve the problem related with toxicity of an organotin compound, and to obtain a cyclic compound at a high yield. A method for coupling carbon atoms in an unsaturated hydrocarbon compound molecule comprises a step of carrying out in-situ reaction of an allyl substituent of the following formula 3 or 4 containing an unsaturated hydrocarbon compound with indium halide and a tertiary amine represented by the formula of NR2R3R4, in the presence of a palladium catalyst to form an allyl indium compound in which Z of the allyl substituent of formula 3 or 4 is substituted with indium, thereby providing a cyclic compound having a vinyl substituent represented by the following formula 1 or formula 2 through an in-situ intramolecular cyclization reaction. In the above formulae, X is Cl, Br or I; Y is (CH2)pCR11R12, NR13 or (CH2)qONR14; Z is Cl, Br, I, OAc or OCO2CH3; each of A, B, C and D independently represents H, a C1-C5 alkyl, phenyl or benzyl, or A and B or C and D are linked to each other via a C2-C10 alkylene, C2-C5 alkenylene, fused ring-containing C2-C10 alkylene or fused ring-containing C2-C5 alkenylene to form a ring optionally further comprising at least one heteroatom selected from N, O and S; R1 represents H, fluorine-substituted or non-substituted C1-C5 alkyl, C1-C5 alkoxy, C1-C5 alkoxycarbonyl or C1-C5 alkoxycarbonyl; each of R2, R3 and R4 represents a C1-C5 alkyl, phenyl or benzyl; each of R11 and R12 represents H, a C1-C5 alkyl, C1-C5 alkoxy, C1-C5 alkylcarbonyl or C1-C5 alkoxycarbonyl; R13 is a C1-C5 alkyl or SO2R21; R14 is t-butoxycarbonyl or a C1-C5 alkyl; R21 is a C1-C5 alkyl or phenyl; n is an integer of 1-4; m is an integer of 1-3; p is an integer of 0-5; and q is an integer of 1-3.