toluene, 100 deg C, 17 h; Yield given. Multistep reaction. Further byproducts given. Yields of byproduct given;
参考文献
Benati, Luisa; Montevecchi, P. Carlo; Spagnolo, Piero
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1991 , # 1 p. 71 - 77
acetonitrile, 60 deg C, 48 h; Yield given. Multistep reaction. Further byproducts given. Yields of byproduct given;
参考文献
Benati, Luisa; Montevecchi, P. Carlo; Spagnolo, Piero
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1991 , # 1 p. 71 - 77
Aldersley, Michael F.; Dean, Francis M.; Nayyir-Mazhir, Rassoul
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1983 , # 8 p. 1753 - 1757
Aldersley, Michael F.; Dean, Francis M.; Nayyir-Mazhir, Rassoul
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1983 , # 8 p. 1753 - 1757
in acetonitrile
24 h; other pyridinium ylides, other substituted naphthoquinones; Mechanism;
参考文献
Aldersley, Michael F.; Chishti, Shuhid H.; Dean, Francis M.; Douglas, Mark E.; Ennis, David S.
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1990 , # 8 p. 2163 - 2174
18-crown-6 ether; potassium carbonate in dichloromethane
10 h;
参考文献
Aldersley, Michael F.; Dean, Francis M.; Nayyir-Mazhir, Rassoul
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1983 , # 8 p. 1753 - 1757
1: 5.25 g / conc.nitric acid, conc.sulphuric acid / 0.75 h / 60 - 80 °C
2: 66 percent / diethyl ether
View Scheme
参考文献
Boyle, Peter H.; O'Mahony, Mary J.; Cardin, Christine J.
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1984 , # 4 p. 593 - 601
