±±¾©Ê¯ÓÍ»¯¹¤Ñ§Ôº2026ÄêÑо¿ÉúÕÐÉú½ÓÊÕµ÷¼Á¹«¸æ
²é¿´: 808  |  »Ø¸´: 1
±¾Ìû²úÉú 1 ¸ö ·­ÒëEPI £¬µã»÷ÕâÀï½øÐв鿴

83908458

Òø³æ (СÓÐÃûÆø)

[½»Á÷] ÓлúÓ¢ÎÄÕªÒª£¬ÇóÖú

ÇóÖú£¡£¡ÏÂÎçÒª½»²îÁË£¬µ«ÊÇÓеãÄѰìµÄÊÂÇéûʱ¼ä·­ÒëÁË
ÄÄλÅóÓÑÄܰïæ·­ÒëÏ£¬¸Ð¼¤²»¾¡£¡£¡  ÔÚÏßµÈ £¬ лл¸÷λÁË£¡£¡

The use of NaBH4-H2SO4 for the reduction of ¦Á-amino acids to the corresponding amino alcohols offers definite advantages: i) operational simplicity, ii) ease of scaling up the reaction without risking explosion, and iii) use of the inexpensive reagents. During the course of our recent studies of bisoxazoline chemistry[1] we need to develop a convenient and reliable procedure for the mole-scale synthesis of ¦Á,¦Â-amino alcohols from the corresponding ¦Á-amino acids. Although there exist several methods[2], including those described in Organic Syntheses,(and also some amino alcohols are commercially available) these methods require the use of rather expensive reagents (e.g.,LiBH4, BH3-SMe2) and/or careful control of reaction conditions to minimize the risk of explosion that may occur after the induction period. We recommend herein the use of the two inexpensive reagents, NaBH4 and H2SO4, as exemplified by the reduction of D-phenylglycine.

» ²ÂÄãϲ»¶

ÒÑÔÄ   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

jingjing1005

ľ³æ (СÓÐÃûÆø)

¡ï ¡ï ¡ï ¡ï
bancage(½ð±Ò+3):ÐÁ¿àÐÁ¿à ºÇºÇ 2010-05-28 19:17:50
wypward(½ð±Ò+1):»¶Ó­Ð³æ 2010-05-28 19:22:17
83908458(½ð±Ò+15, ·­ÒëEPI+1):·Ç³£¸Ðл£¬ÓиöµØ·½ÎÒһֱŪ²»Ã÷°×£¬¿´ÁËÄãдµÄ£¬£¬ Ô­À´ÊÇÕâÑù¡­¡­ Ó¢ÓïÓï·¨ÕæÖØÒª 2010-05-29 00:34:32
ʹÓÃNaBH4-H2SO4ÒÔ¼õÉÙÏàÓ¦°±»ù´¼µÄ¦Á-°±»ùËáÓÃÁ¿¾ßÓÐÒ»¶¨µÄÓŵ㣺i) ²Ù×÷¼òµ¥£¬ii) ±ãÓÚ·´Ó¦µÄ·Å´ó£¬Í¬Ê±±ÜÃâÁ˱¬Õ¨µÄΣÏÕ£¬iii) ÓÃÁ®¼ÛµÄ·´Ó¦ÊÔ¼Á¡£ÔÚË«¶ñßòßø»¯Ñ§µÄ×îÐÂÑо¿¹ý³ÌÖУ¬ÎÒÃÇÐèÒª¿ª·¢Ò»ÖÖ·½±ã¡¢¿É¿¿µÄĦ¶û¼¶±ðºÏ³É·´Ó¦ÒÔ±ã´ÓÏàÓ¦µÄ¦Á-°±»ùËáµÃµ½¦Á,¦Â-amino alcohols¡£¾¡¹ÜĿǰÓм¸Öֿɹ©Ñ¡ÔñµÄ·½·¨£¬°üÀ¨ÔÚÓлúºÏ³ÉÔÓÖ¾ÖÐÌáµ½¹ýµÄ£¨ÒÔ¼°Ò»Ð©ÊÐÊÛ°±»ù´¼µÄºÏ³É·½·¨£©£¬µ«ÊÇÕâЩ·½·¨¶¼ÐèÒªÓõ½°º¹óµÄÊÔ¼Á£¨ÈçLiBH4, BH3-SMe2£©£¬¶øÇÒ±ØÐëСÐÄ¼à¿Ø·´Ó¦Ìõ¼þÒÔ¼õСÔÚÓÕµ¼ÆÚ±¬Õ¨µÄ·çÏÕ¡£Òò´ËÒÔNaBH4-H2SO4¶ÔD -±½¸Ê°±ËáµÄ»¹Ô­ÎªÀýÖ¤£¬ÎÒÃÇÍÆ¼öʹÓÃNaBH4-H2SO4ÕâÁ½ÖÖÁ®¼ÛµÄÊÔ¼Á¡£
2Â¥2010-05-28 17:18:35
ÒÑÔÄ   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
Ïà¹Ø°æ¿éÌø×ª ÎÒÒª¶©ÔÄÂ¥Ö÷ 83908458 µÄÖ÷Ìâ¸üÐÂ
×î¾ßÈËÆøÈÈÌûÍÆ¼ö [²é¿´È«²¿] ×÷Õß »Ø/¿´ ×îºó·¢±í
[¿¼ÑÐ] 349Çóµ÷¼Á +5 ½Ü˹ËþÀï˹ 2026-03-21 5/250 2026-03-27 00:31 by wxiongid
[¿¼ÑÐ] 329Çóµ÷¼Á +5 1() 2026-03-22 5/250 2026-03-26 20:40 by fmesaito
[¿¼ÑÐ] ¡¾Ë«Ò»Á÷ԺУÐÂÄÜÔ´¡¢»·¾³²ÄÁÏ£¬²ÄÁϼӹ¤ÓëÄ£ÄâÕÐÊÕ´óÁ¿µ÷¼Á¡¿ +4 Higraduate 2026-03-22 8/400 2026-03-26 20:34 by Higraduate
[¿¼ÑÐ] ѧ˶274Çóµ÷¼Á +3 LiÀîÓã 2026-03-26 3/150 2026-03-26 18:32 by Ìá³ö·½·¨µÄÌá³öº
[¿¼ÑÐ] Öйú¿ÆÑ§ÔºÉîÛÚÏȽø¼¼ÊõÑо¿Ôº-¹âÏË´«¸Ð¿ÎÌâ×éÕÐÉú-Öйú¿ÆÑ§Ôº´óѧ¡¢ÉîÛÚÀí¹¤´óѧÁªÅà +5 YangTyu1 2026-03-26 5/250 2026-03-26 18:27 by èßäèßäѽ
[¿¼ÑÐ] Ò»Ö¾Ô¸±±¾©»¯¹¤´óѧ²ÄÁÏÓ뻯¹¤ 264·Ö¸÷¿Æ¹ýAÇø¹ú¼ÒÏß +6 ¹þ¹þ157349 2026-03-21 6/300 2026-03-26 10:39 by ×íÔÚ·çÀï
[¿¼ÑÐ] ²ÄÁϵ÷¼Á +3 iwinso 2026-03-23 3/150 2026-03-25 11:29 by greychen00
[¿¼ÑÐ] 318Çóµ÷¼Á +3 plumÀî×Ó 2026-03-23 3/150 2026-03-25 09:42 by ÎíÉ¢ºóÏàÓölc
[¿¼ÑÐ] ÉúÎïѧѧ˶Çóµ÷¼Á +7 СÑò˯×ÅÁË? 2026-03-23 10/500 2026-03-25 02:24 by Çå·ç·÷Ñï¡£ m
[¿¼ÑÐ] ʳƷר˶ һ־Ը˫һÁ÷ 328 +3 xiaom99 2026-03-21 4/200 2026-03-24 21:20 by lailaisimei
[¿¼ÑÐ] ²ÄÁÏ¿¼Ñе÷¼ÁÉú +3 »ÆÁ»Ò»ÃÎǧÄê 2026-03-24 3/150 2026-03-24 17:00 by barlinike
[¿¼ÑÐ] 277·ÖÇóµ÷¼Á£¬¿çµ÷²ÄÁÏ +3 ¿¼Ñе÷¼Álxh 2026-03-24 3/150 2026-03-24 13:52 by JourneyLucky
[¿¼ÑÐ] 284Çóµ÷¼Á +3 yanzhixue111 2026-03-23 6/300 2026-03-23 22:58 by pswait
[¿¼ÑÐ] 293Çóµ÷¼Á +3 ÌÎÌÎWjt 2026-03-22 5/250 2026-03-22 22:21 by jiangpengfei
[¿¼ÑÐ] ʯºÓ×Ó´óѧ£¨211¡¢Ë«Ò»Á÷£©Ë¶²©Ñо¿Éú³¤ÆÚÕÐÉú¹«¸æ +3 Àî×ÓÄ¿ 2026-03-22 3/150 2026-03-22 21:01 by ÔõôÊÍ»³
[¿¼ÑÐ] 275Çóµ÷¼Á +6 shansx 2026-03-22 8/400 2026-03-22 15:27 by barlinike
[¿¼ÑÐ] ³õÊÔ 317 +7 °ëÀ­Ô±û 2026-03-20 7/350 2026-03-21 22:26 by peike
[¿¼ÑÐ] Çóµ÷¼Á +3 13341 2026-03-20 3/150 2026-03-21 18:28 by ѧԱ8dgXkO
[¿¼ÑÐ] 266Çóµ÷¼Á +3 ÍÛºôºßºôºß 2026-03-20 3/150 2026-03-21 16:46 by barlinike
[¿¼ÑÐ] 330Çóµ÷¼Á0854 +3 assdll 2026-03-21 3/150 2026-03-21 13:01 by ²«»÷518
ÐÅÏ¢Ìáʾ
ÇëÌî´¦ÀíÒâ¼û