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Facial selectivity refers to selectivity of the side of a pro-chiral molecule. For example acetophenone - addition of hydride to the "re" side of acetophenone gives rise to the R isomer of phenylethanol, wheras addition to the "si" side gives rise to the S isomer. ·ÒëµÄÌ«ÀëÆ×²»¸ø½ð±Ò£¬²»Òª¸øÎÒµ·ÂÒ |
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- ½ð±Ò: 1423.7
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- ÔÚÏß: 43.9Сʱ
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- ×¢²á: 2009-12-23
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·¢Ñ¿ÍÁ¶¹(½ð±Ò+1):лл²ÎÓë 2010-06-14 11:06:26
wypward(½ð±Ò+1):лл²ÎÓë 2010-06-14 11:41:59
Äý¾²2009(½ð±Ò+2, ·ÒëEPI+1): 2010-06-14 13:10:03
·¢Ñ¿ÍÁ¶¹(½ð±Ò+1):лл²ÎÓë 2010-06-14 11:06:26
wypward(½ð±Ò+1):лл²ÎÓë 2010-06-14 11:41:59
Äý¾²2009(½ð±Ò+2, ·ÒëEPI+1): 2010-06-14 13:10:03
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