反应条件
1.1: 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione / dimethyl sulfoxide; dichloromethane / 3 h / 20 °C
2.1: R-(+)-proline / chloroform / 2 h / 0 °C
2.2: 2 h / 0 °C
3.1: acetic acid; zinc / ethanol / 12 h / 20 °C
4.1: di(n-butyl)tin oxide; triethylamine / dichloromethane / 0 - 20 °C
5.1: lithium aluminium tetrahydride / tetrahydrofuran / |Reflux; |Inert atmosphere
6.1: 1H-imidazole / dichloromethane / 0.17 h / 0 °C
6.2: 6 h / 0 - 20 °C
7.1: 2,3-dicyano-5,6-dichloro-p-benzoquinone / dichloromethane; water / 2 h / 0 - 20 °C
8.1: 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione / dimethyl sulfoxide; dichloromethane / 3 h / 20 °C
9.1: (S)-(minus;)-1,1'-bi-2-naphthol; titanium (IV) isopropoxide / dichloromethane / 0.5 h / 20 °C / |Inert atmosphere; |Molecular sieve
9.2: 24 h / -78 - -20 °C / |Inert atmosphere; |Molecular sieve
10.1: 4-(N,N-dimethlyamino)pyridine / 1 h / 0 - 20 °C / |Inert atmosphere
11.1: Grubb's 2nd generation catalyst / dichloromethane
12.1: 0.5 h / 0 - 20 °C
View Scheme
参考文献
Sabitha, Gowravaram; Reddy, K. Purushotham; Reddy, S. Purushotham; Yadav
Tetrahedron Letters, 2014 , vol. 55, # 21 p. 3227 - 3228