| ²é¿´: 296 | »Ø¸´: 0 | ||
Ayio--гæ (³õÈëÎÄ̳)
|
[ÇóÖú]
ÇóÖú~»¯Ñ§Ïà¹ØÎÄÏ×·Ò룬ӢÒëÖУ¬Ð»Ð»£¡
|
|
A general synthesis of indol-2(3H)-ones (oxindoles), was developed based on the addition of dimethyl malonate to comrnercially available halonitrobenzenes. The advantage of this route over many other oxindole syntheses was the regiochemical control of the substitution pattern on the aromatic ring. ¡¡¡¡¡¡¡¡ |
» ±¾Ìû¸½¼þ×ÊÔ´Áбí
-
»¶Ó¼à¶½ºÍ·´À¡£ºÐ¡Ä¾³æ½öÌṩ½»Á÷ƽ̨£¬²»¶Ô¸ÃÄÚÈݸºÔð¡£
±¾ÄÚÈÝÓÉÓû§×ÔÖ÷·¢²¼£¬Èç¹ûÆäÄÚÈÝÉæ¼°µ½ÖªÊ¶²úȨÎÊÌ⣬ÆäÔðÈÎÔÚÓÚÓû§±¾ÈË£¬Èç¶Ô°æÈ¨ÓÐÒìÒ飬ÇëÁªÏµÓÊÏ䣺xiaomuchong@tal.com - ¸½¼þ 1 : A_General_Oxindole_Synthesis.pdf
2016-04-25 12:58:23, 231.01 K
» ²ÂÄãϲ»¶
ÉúÎïѧ308·ÖÇóµ÷¼Á£¨Ò»Ö¾Ô¸»ª¶«Ê¦´ó£©
ÒѾÓÐ12È˻ظ´
µ÷¼ÁÇóÖú£¨ÉúÎïÓëÒ½Ò©£©
ÒѾÓÐ3È˻ظ´
Ò»Ö¾Ô¸¼ª´ó»¯Ñ§327Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
Ò»Ö¾Ô¸ÉúÎïÓëÒ½Ò©£¬296·Ö£¬Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
327Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
³õÊÔ301£¬´úÂë085701»·¾³¹¤³Ì£¬±¾Ë¶Ò»Ö£¬ËÄÁù¼¶Òѹý£¬ÓжþÇøÒ»×÷£¬¹²·¢±í5ƪÂÛÎÄ
ÒѾÓÐ8È˻ظ´
327¿¼Ñе÷¼ÁÍÆ¼ö
ÒѾÓÐ6È˻ظ´
328Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
304Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
»¯¹¤Çóµ÷¼Á£¡
ÒѾÓÐ16È˻ظ´














»Ø¸´´ËÂ¥