| ²é¿´: 534 | »Ø¸´: 1 | ||
| ±¾Ìû²úÉú 1 ¸ö ·ÒëEPI £¬µã»÷ÕâÀï½øÐв鿴 | ||
lgq101ľ³æ (СÓÐÃûÆø)
|
[ÇóÖú]
Çó·ÒëʵÑé¹ý³Ì~~~лл
|
|
| General Procedure for Evans Butadiene [4 + 2 + 2] Cycloaddition (7). Vacuum-dried resin 3 (800 mg, 0.86 meq, 1.0 eq) was swollen with CH2Cl2 (20 mL) for 10 min, then cooled to 0 ¡ãC. Solid m-CPBA (580 mg, 2.58 mmol, 3.0 eq) was added and the reaction was stirred at 0 ¡ãC for 1 h, then allowed to warm to RT and stirred for 6 h. The resin was washed and dried, then swollen with toluene (20mL) for 10min. A stock solution of Rh(IMes)(COD)Cl4, where IMes is 1,3-bis(2,4,6-trimethylphenyl)imidazoly-2-ylidene, and AgOTf (1¡Ã2 molar ratio, 0.1 M Rh in degassed toluene, 3.44 mL, 0.34 mmol Rh, 0.4 eq) was added to the resin, and the reaction atmosphere was flushed with 1,3-butadiene gas, then the mixture was stirred under a balloon of 1,3-butadiene at RT for 2 h, refilling the balloon when empty. The balloon was removed and the mixture was heated to 108 ¡ãC for 24 h. The resin was cooled, washed, and dried to afford cyclooctapyrrolidines 7. |
» ²ÂÄãϲ»¶
»úе¹¤³Ì264ѧ˶Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
264Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
22408 266Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
273Çóµ÷¼Á
ÒѾÓÐ43È˻ظ´
307Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
327Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
338Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
326·Ö£¬Ò»Ö¾Ô¸»¦9£¬ÇóÉúÎïѧµ÷¼Á
ÒѾÓÐ3È˻ظ´

1986
Ìú¸Ëľ³æ (ÖªÃû×÷¼Ò)
ҩͯ
- ·ÒëEPI: 26
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 8305.5
- É¢½ð: 43
- ºì»¨: 7
- ɳ·¢: 302
- Ìû×Ó: 5662
- ÔÚÏß: 312.8Сʱ
- ³æºÅ: 1195378
- ×¢²á: 2011-01-24
- ÐÔ±ð: GG
- רҵ: ÓлúºÏ³É
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï
ringzhu(½ð±Ò+1): ¶àл½»Á÷~~ 2011-06-05 12:10:57
lgq101(½ð±Ò+10, ·ÒëEPI+1): лл~~~ 2011-06-05 21:44:12
ringzhu(½ð±Ò+1): ¶àл½»Á÷~~ 2011-06-05 12:10:57
lgq101(½ð±Ò+10, ·ÒëEPI+1): лл~~~ 2011-06-05 21:44:12
|
General Procedure for Evans Butadiene [4 + 2 + 2] Cycloaddition (7). ºÏ³ÉEvans Butadiene [4 + 2 + 2] Cycloaddition (7)µÄÒ»°ãʵÑé²½Öè¡£ Vacuum-dried resin 3 (800 mg, 0.86 meq, 1.0 eq) was swollen with CH2Cl2 (20 mL) for 10 min, then cooled to 0 ¡ãC. Õæ¿Õ¸ÉÔï¹ýµÄÊ÷Ö¬3(800 mg, 0.86 meq, 1.0 eq)ÔÚ20ºÁÉýµÄ¶þÂȼ×ÍéÖÐÈܽâ10·ÖÖÓÖ®ºó½µÎµ½0¶È£¬ Solid m-CPBA (580 mg, 2.58 mmol, 3.0 eq) was added and the reaction was stirred at 0 ¡ãC for 1 h, then allowed to warm to RT and stirred for 6 h. ¹ÌÌåm-CPBA (580 mg, 2.58 mmol, 3.0 eq)ÔÚ0¶È¼ÓÈëµ½ÉÏÊö·´Ó¦ÒºÖУ¬¼ÌÐø½Á°è1¸öСʱ£¬ÔÙÉýµ½ÊÒνÁ°è6¸öСʱ£¬ The resin was washed and dried, then swollen with toluene (20mL) for 10min¡£ ·´Ó¦ÒºÏ´µÓ£¬¸ÉÔÔÙ´ÎÈܽâÔÚ20ºÁÉýµÄ¼×±½ÖУ¬10·ÖÖÓÖ®ºó£¬ A stock solution of Rh(IMes)(COD)Cl4, where IMes is 1,3-bis(2,4,6-trimethylphenyl)imidazoly-2-ylidene, and AgOTf (1¡Ã2 molar ratio, 0.1 M Rh in degassed toluene, 3.44 mL, 0.34 mmol Rh, 0.4 eq) was added to the resin, ½«×¼±¸ºÃµÄRh(IMes)(COD)Cl4ºÍAgOTf (1¡Ã2 molar ratio, 0.1 M Rh in degassed toluene, 3.44 mL, 0.34 mmol Rh, 0.4 eq)¼Óµ½·´Ó¦ÖУ¬ÆäÖÐIMesÊÇÖ¸1,3-bis(2,4,6-trimethylphenyl)imidazoly-2-ylidene and the reaction atmosphere was flushed with 1,3-butadiene gas, then the mixture was stirred under a balloon of 1,3-butadiene at RT for 2 h, refilling the balloon when empty. ÏòÆøÇòÖгäÂú1,3-butadiene£¬²¢Öû»·´Ó¦ÌåϵÖÐµÄÆøÌ壬µ±ÆøÇò¿ÕÁË£¬ÖØÐ³äÂú£¬ÔÚÊÒÎÂÏ·´Ó¦2Сʱ֮ºó£¬ The balloon was removed and the mixture was heated to 108 ¡ãC for 24 h. The resin was cooled, washed, and dried to afford cyclooctapyrrolidines 7. ½«ÆøÇòÈ¡×ߣ¬·´Ó¦¼ÓÈȵ½108¶È·´Ó¦24Сʱ£¬½µÎ£¬Ï´µÓ£¬¸ÉÔµÃµ½ÁËcyclooctapyrrolidines 7¡£ |
2Â¥2011-06-05 11:48:07














»Ø¸´´ËÂ¥