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2018-12-08 14:51發(fā)布了問(wèn)答
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藥物過(guò)敏怎么辦 黃胺類藥物過(guò)敏怎么辦
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2018-11-28 15:45發(fā)布了問(wèn)答
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消膽胺的消膽胺
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2017-09-09 08:00發(fā)布了問(wèn)答
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降壓藥苯磺酸氨氯地平片一天吃四分之一顆還有用嗎?
- 去年4月份得了心肌炎,后來(lái)一直服藥到12月底時(shí)復(fù)查說(shuō)心肌炎癥狀沒(méi)有了,但是血壓高,做過(guò)動(dòng)態(tài)血壓,醫(yī)生說(shuō)患了高血壓,一直服用苯磺酸氨氯地平片,現(xiàn)在已經(jīng)一天只服用四分之一片,血壓基本維持在100-110/60-75,請(qǐng)問(wèn)可以停藥嗎?
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2017-04-26 00:33發(fā)布了問(wèn)答
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洋河封藏大典上提到的“三老、兩多、數(shù)量少”是什么意思?
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2017-03-26 12:18發(fā)布了問(wèn)答
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醚類,酮類有哪些物理和化學(xué)性質(zhì)
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2017-02-23 17:55發(fā)布了問(wèn)答
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褪黑素能與歸脾顆粒一起吃嗎
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2016-10-22 11:09發(fā)布了問(wèn)答
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洗衣液,aes,磺酸,體系可以用椰油酸鉀皂嗎
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2016-09-25 22:26發(fā)布了問(wèn)答
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灌封膠的區(qū)別
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2015-12-23 21:17發(fā)布了問(wèn)答
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一周三根煙危害大嗎
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2012-11-22 12:57發(fā)布了問(wèn)答
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腈基和羥基生成的化合物是什么
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2012-08-31 01:19發(fā)布了問(wèn)答
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文獻(xiàn)求翻譯
- Since the formation of a titanacyclopropane en route to cyclopropylamines can only occur with alkylmagnesium halides that contain a b-hydrogen atom, Grignard reagents without b-hydrogens appeared to be the most promising reagents for th... Since the formation of a titanacyclopropane en route to
cyclopropylamines can only occur with alkylmagnesium
halides that contain a b-hydrogen atom, Grignard reagents
without b-hydrogens appeared to be the most promising
reagents for the synthesis of primary tert-alkylamines
from nitriles (Scheme 1). Thus propionitrile (1a), phenylmagnesium
bromide (2) and Ti(Oi-Pr)4 were chosen to
optimize the reaction conditions. In the protocol for the
synthesis of cyclopropylamines,10 Ti(Oi-Pr)4 is already
present in the diethyl ether solution of a nitrile, before two
equivalents of the Grignard reagent are added. As this did
not appear to be optimal for the synthesis of primary tertalkylamines,
the Grignard reagent was added before
Ti(Oi-Pr)4. With 2 equivalents of PhMgBr, 0.1 equivalent
of Ti(Oi-Pr)4, and 1 equivalent of propionitrile (1a), the
primary tert-alkylamine 8a was not formed at all. With an
equimolar quantity of Ti(Oi-Pr)4, the amine 8a was produced
in a low yield (11%) but with 1 equivalent of Ti(Oi-
Pr)4 and 3 equivalents of the Grignard reagent 2, a 60%
yield of 8a was obtained. Monitoring of the reaction by
workup of aliquots of the reaction mixture showed that the
first addition of 2 to form the N-magnesio derivative of the
corresponding imine was rapid, whereas the subsequent
second addition of the Grignard reagent 2 required heating
under reflux for up to 24 hours. In tetrahydrofuran instead
of diethyl ether, the amine 8a was formed in a very low
yield, if at all. 展開
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2007-07-23 01:05發(fā)布了問(wèn)答
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何謂----美拉德反應(yīng)?
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2007-03-31 05:28發(fā)布了問(wèn)答
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α-脫羧是什么意思
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