K was first synthesized via the Condensation of 2-hydroxy-3-prenyl-4, 6-dimethoxymethoxyacetophenone 3- methoxy-4methoxymethoxybenzaldehyde followed by cyclixation
Methoxy-5′-prenylnaringenin was first synthesized via the condensation of 2-hydroxy- 4, 6-dimethoxymethoxyacetophenone with 3 - methoxy - 4 - methoxymethoxy- 5- prenylbenzaldehyde followed by cyclization and demet...Methoxy-5′-prenylnaringenin was first synthesized via the condensation of 2-hydroxy- 4, 6-dimethoxymethoxyacetophenone with 3 - methoxy - 4 - methoxymethoxy- 5- prenylbenzaldehyde followed by cyclization and demethoxymethylation .展开更多
Methylenedloxyisodericine-A and pongapinone-B were first synthesized via thecondensation of plperonal with 2-hydroxy-4-methoxy-3-prenylactophenone and 4, 6-dimethoxy-2-hydroxy 3-prenylacetophonone respectively follow...Methylenedloxyisodericine-A and pongapinone-B were first synthesized via thecondensation of plperonal with 2-hydroxy-4-methoxy-3-prenylactophenone and 4, 6-dimethoxy-2-hydroxy 3-prenylacetophonone respectively followed by cyclization.展开更多
Three 3, 3'-biflavones were synthesized by using iodination of flavones through I-2-CAN system as the key step followed by the coupling of 3-iodoflavones under the Ullmann reaction conditions.
文摘K was first synthesized via the Condensation of 2-hydroxy-3-prenyl-4, 6-dimethoxymethoxyacetophenone 3- methoxy-4methoxymethoxybenzaldehyde followed by cyclixation
文摘Methoxy-5′-prenylnaringenin was first synthesized via the condensation of 2-hydroxy- 4, 6-dimethoxymethoxyacetophenone with 3 - methoxy - 4 - methoxymethoxy- 5- prenylbenzaldehyde followed by cyclization and demethoxymethylation .
文摘Methylenedloxyisodericine-A and pongapinone-B were first synthesized via thecondensation of plperonal with 2-hydroxy-4-methoxy-3-prenylactophenone and 4, 6-dimethoxy-2-hydroxy 3-prenylacetophonone respectively followed by cyclization.
文摘Three 3, 3'-biflavones were synthesized by using iodination of flavones through I-2-CAN system as the key step followed by the coupling of 3-iodoflavones under the Ullmann reaction conditions.
