Pd(0) Complex prepared from Pd(dba)(2) and chiral quinolinyl-oxazoline ligand can catalyze alkylation and cyclization reaction of 1, 4-dichlorobut-2-ene 1 with anion of N-(diphenylmethylene)amino acetonitrile 2 to pro...Pd(0) Complex prepared from Pd(dba)(2) and chiral quinolinyl-oxazoline ligand can catalyze alkylation and cyclization reaction of 1, 4-dichlorobut-2-ene 1 with anion of N-(diphenylmethylene)amino acetonitrile 2 to provide (E)-2-ethenyl-1-N-(diphenylmethylene) amino cyclopropane carbonitrile 3 with 100% de and 20% cc. Reduction of (E)-3 by diimide followed by acidic hydrolysis afforded (1S, 2S)-2-ethyl-1-aminocyclopropanecarboxylic acid 9, a natural product coronamic acid.展开更多
The reactions of 5-methyl-3-hydroxyisoxazole with 2, 2-dimethyl, 3-substituted cyclopropanecarboxylic chlorides give O-acyl-5-methyl-3-hydroxyisoxazole and N-acyl-5-methylisoxazolin-3-one derivatives. The ratio of O-a...The reactions of 5-methyl-3-hydroxyisoxazole with 2, 2-dimethyl, 3-substituted cyclopropanecarboxylic chlorides give O-acyl-5-methyl-3-hydroxyisoxazole and N-acyl-5-methylisoxazolin-3-one derivatives. The ratio of O-acyl to N-acyl product depends upon the acylation reagents. O-acyl derivatives can be converted to the N-acyl compounds by isomerization under acidic conditions or heating.展开更多
Cyclopropanecarboxylic acid or 2,2-dimethyl cyclopropanecarboxylic acid was used as a leading compound for its biological activity. Six new N-（substituted） cyclopropanecarboxyl-N＇-pyridin-2-yl thioureas were prepar...Cyclopropanecarboxylic acid or 2,2-dimethyl cyclopropanecarboxylic acid was used as a leading compound for its biological activity. Six new N-（substituted） cyclopropanecarboxyl-N＇-pyridin-2-yl thioureas were prepared. Compound 5 was obtained by oxidizing cyclization of compound 4 in the presence of bromine in chloroform solution. The structures of 4 and 5 were confirmed by 1H NMR and elemental analysis. The preliminary biological tests indicate that compound 4b and 4e have excellent herbicidal activity, and compound 4e and 4f have excellent fungicidal activity.展开更多
基金the National Natural Science Foundation of Chinathe Major State Basic Research Development Program(grant No.G2000077506)the Ministry of Education of China for the financial support.
文摘Pd(0) Complex prepared from Pd(dba)(2) and chiral quinolinyl-oxazoline ligand can catalyze alkylation and cyclization reaction of 1, 4-dichlorobut-2-ene 1 with anion of N-(diphenylmethylene)amino acetonitrile 2 to provide (E)-2-ethenyl-1-N-(diphenylmethylene) amino cyclopropane carbonitrile 3 with 100% de and 20% cc. Reduction of (E)-3 by diimide followed by acidic hydrolysis afforded (1S, 2S)-2-ethyl-1-aminocyclopropanecarboxylic acid 9, a natural product coronamic acid.
基金Supposed by the National Natural Science Foundation of China
文摘The reactions of 5-methyl-3-hydroxyisoxazole with 2, 2-dimethyl, 3-substituted cyclopropanecarboxylic chlorides give O-acyl-5-methyl-3-hydroxyisoxazole and N-acyl-5-methylisoxazolin-3-one derivatives. The ratio of O-acyl to N-acyl product depends upon the acylation reagents. O-acyl derivatives can be converted to the N-acyl compounds by isomerization under acidic conditions or heating.
文摘Cyclopropanecarboxylic acid or 2,2-dimethyl cyclopropanecarboxylic acid was used as a leading compound for its biological activity. Six new N-（substituted） cyclopropanecarboxyl-N＇-pyridin-2-yl thioureas were prepared. Compound 5 was obtained by oxidizing cyclization of compound 4 in the presence of bromine in chloroform solution. The structures of 4 and 5 were confirmed by 1H NMR and elemental analysis. The preliminary biological tests indicate that compound 4b and 4e have excellent herbicidal activity, and compound 4e and 4f have excellent fungicidal activity.
