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[À¯±âÈÇнÇÇè1] ½ÇÇè8 °á°ú·¹Æ÷Æ® stereospecific Preparation 2. intramolecular SN2 reaction of bromohydrin to epoxide / 1. ½ÇÇèÁ¦¸ñ 2. ½ÇÇè°á°ú 3. ÅäÀÇ 4. Âü°í¹®Çå / 1. ½ÇÇèÁ¦¸ñ ½ÇÇè Á¦¸ñÀº `Intramolecular SN2 Reaction of Bromohydrin to Epoxide`ÀÌ´Ù. ÀÌ ¹ÝÀÀÀº À¯±â ÈÇп¡¼ Áß¿äÇÑ ¹ÝÀÀ À¯Çü Áß Çϳª·Î, ºê·Î¸ðÈ÷µå¸°ÀÌ ³»Á¢ SN2 ¹ÝÀÀÀ» ÅëÇØ ¿¡Æø»çÀ̵å·Î Àü¡¦ |
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[À¯±âÈÇнÇÇè1] ½ÇÇè8 ¿¹ºñ·¹Æ÷Æ® stereospecific Preparation 2. intramolecular SN2 reaction of bromohydrin to epoxide / 1.½ÇÇèÁ¦¸ñ 2.½ÇÇ賯¥ 3.½ÇÇè¸ñÀû 4.½ÇÇèÀÌ·Ð 5.½Ã¾à ¹× ±â±¸ 6.½ÇÇè¹æ¹ý 7.Âü°í¹®Çå / 1.½ÇÇèÁ¦¸ñ ½ÇÇè Á¦¸ñÀº `Intramolecular SN2 ¹ÝÀÀÀ» ÅëÇÑ BromohydrinÀÇ Epoxide·ÎÀÇ ½ºÅ×·¹¿À½ºÆä½ÃÇÈ ÇÕ¼º`ÀÌ´Ù. ÀÌ ½ÇÇèÀº À¯±âÈÇп¡¼ Áß¿äÇÑ ¹ÝÀÀ ¸ÞÄ¿¡¦ |
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[À¯±âÈÇнÇÇè1] ½ÇÇè7 °á°ú·¹Æ÷Æ® stereospecific Preparation 1. Bromohydrin formation of cyclohexane / 1. ½ÇÇèÁ¦¸ñ 2. ½ÇÇè°á°ú 3. ÅäÀÇ 4. Âü°í¹®Çå / 1. ½ÇÇèÁ¦¸ñ ½ÇÇè Á¦¸ñÀº ¡®Bromohydrin formation of cyclohexane¡¯ÀÌ´Ù. ÀÌ ½ÇÇèÀº »çÀÌŬ·ÎÇí»êÀÇ ºê·Î¸ðÇÏÀ̵帰 ÈÇÕ¹°ÀÇ Á¤ stereospecific ÇÕ¼ºÀ» ´Ù·ç°í ÀÖ´Ù. ºê·Î¸ðÇÏÀ̵帰Àº ÇÒ·ÎÁ¨°ú ÇÏÀ̵å·Ï½Ç ±â°¡ µ¿½Ã¿¡¡¦ |
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[À¯±âÈÇнÇÇè1] ½ÇÇè7 ¿¹ºñ·¹Æ÷Æ® stereospecific Preparation 1. Bromohydrin formation of cyclohexane / 1.½ÇÇèÁ¦¸ñ 2.½ÇÇ賯¥ 3.½ÇÇè¸ñÀû 4.½ÇÇèÀÌ·Ð 5.½Ã¾à ¹× ±â±¸ 6.½ÇÇè¹æ¹ý 7.Âü°í¹®Çå / 1.½ÇÇèÁ¦¸ñ ½ÇÇè Á¦¸ñÀº `ºê·Î¸ðÇÏÀ̵帰 Çü¼º ¹ÝÀÀÀ» ÅëÇÑ »çÀÌŬ·ÎÇí¼¼ÀÎÀÇ ÀÔüƯÀÌÀû ÇÕ¼º`ÀÌ´Ù. ÀÌ ½ÇÇèÀº Ưº°È÷ »çÀÌŬ·ÎÇí¼¼Àΰú ºê·Î¹Î, ±×¸®°í ¼ö»êȹ°ÀÌ ¹ÝÀÀÇÏ¿© ºê¡¦ |
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