Global ETD Search

1	A New Approach to Benzo[h]quinoline Skeleton Huang, Chiao-wei 25 July 2007 (has links) We use stepwise [3+3] annulation to prepare the asymmetric glutarimides, and then we can build substituent group in C6 position after choosing regioselective addition reaction. And we establish a new approach to benzo[h]quinoline skeleton starting from glutarimides via ring-closing reaction. Finally, we applied this method to the synthetic studies toward benzo[h]quinoline derivatives. benzo[h]quinoline derivatives regioselective addition reaction [3+3] annulation
2	Synthetic Studies Toward Polysubstituted Pyridin-2-ones and Vitamin B6 Derivatives Chung, Wen-hsuan 19 August 2005 (has links) We can construct asymmetric glutarimide while using [3+3] annulation.Then we can build substituent group in C6 position after choosing regioselective addition reaction, and then apply it to synthetic studies toward polysubstituted pyridin-2-ones and Vitamin B6 derivatives. Vitamin B6 derivatives [3+3] annulation pyridine-2-one regioselective addition reaction
3	1. Synthetic Studies Toward Vitamin B6 Derivatives (dmaPM) and Actinidine 2. Synthetic Studies Toward Piperazine-2,5-diones Skeleton Chung, Wen-Hsuan 04 February 2010 (has links) none pyridin-2-one regioselective addition reaction [3+3] annulation piperazine-2,5-dione Vitamin B6 derivatives dmaPM