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439篇 您的检索式：期刊名="Org Process Dev"

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	题名	作者	年代	出处	被引量
1	Reduction of ethyl benzoylacetate and selective protection of 2- (3-hydroxy-1- phenylpropyl) -4-methylphenol: A new and facile synthesis of tolterodine 显示文摘	De Castro KA Ko J Park D	2007	Org Process Res Dev2007，11，5：	1
2	Large-scale asymmetric synthesis of the 3,6,7,8-tetrahydrochromeno imidazole BYK 405879 : a promising candidate for the treatment of acid-related diseases显示文摘	PALMER A M WEBEL M SCHEUFLER C	2008	Org Process Res Dev2008，12，6：	1
3	Development of a practical,safe,and high-yielding process for the preparation of enantiomerically pure trans-cyclopropane carboxylic acid显示文摘	Singh AK Rao MN Simpson JH	2002	Org Process Res Dev2002，6，：	1
4	Development of a scaleable route for the production of cis-N-benzyl-3- methylamino-4-methylpiperidine 显示文摘	Brown Ripin DH Abele S Cai WL	2003	Org Process Res Dev2003，7，1：	1
5	Large-scale candoxatril asymmetric hydrogenation 显示文摘	BULLIARD M LABOUE B LASTENNET J	2001	Org Process Res Dev2001，5，4：	1
6	Practical large-sacle synthesis of the a-aminomethylpyrrolidin-4-yl-thio-containing side shain of the novel carbapenem antibiotic coripenem显示文摘	Nishino Y Komurasaki T Yuasa T	2003	Org Process Res Dev2003，7，5：	1
7	Fit- for-purpose development of the enabling route to crizotinib(PF-02341066) 显示文摘	Koning PD McAndrew D Moore R	2011	Org Process Res Dev2011，15，5：	1
8	A safe two-step process for manufacturing glyc- idyl nitrate from glycidol involving solid-liquid phase-transfer catalysis显示文摘	Jose R Ochoa-Gomez Juan J Blanco-Gomez	2011	Org Process Res Dev2011，15，6：	1
9	The synthesis of N-aryl-5(S)-aminomethyl-2-oxazolidinone antibacterials and derivatives in one step from aryl carbamates显示文摘	PERRAULT W R PEARLMAN B A GODREJ D B	2003	Org Process Res Dev2003，7，4：	1
10	Large-scale synthesis of ( R )-2-amino-1-( 2-furyl ) ethanol via a chemoenzymatic approach显示文摘	Purkarthofer T Pabst T van den Broek C	2006	Org Process Res Dev2006，10，3：	1
11	Development of a continuous enzymatic process for the preparation of (R)-3-(4-fluorophenyl)-2-hydroxy propionic acid 显示文摘	TAO J McGEE K	2002	Org Process Res Dev2002，6，4：	1
12	Process development for (S,S)-reboxetine succinate via a sharpless asymmetric epoxidation显示文摘	HENEGAR K E CEBULA M	2007	Org Process Res Dev2007，11，3：	1
13	Optimizing fermentation conditions of recombinant Escherichia coli expressing cyclopentanone monooxygenase显示文摘	Alphand V Furstoss R	2006	Org Process Res Dev2006，10，3：	1
14	An efficient enantiopure synthesis of a pivotal precursor to substance P antagonists 显示文摘	Nugent TC Seemayer R	2006	Org Process Res Dev2006，10，1：	1
15	A' second-generation process' for the synthesis of L-neopentylglycine: asymmetric reductive amination using a recombinant whole cell catalyst 显示文摘	Gr6ger H May O Werner H	2006	Org Process Res Dev2006，10，3：	1
16	Investigation of practical routes for the kilogram-scale production of cis-3- methylamino-4-methylpiperidines 显示文摘	Cai WL Colony JL Frost H	2005	Org Process Res Dev2005，9，1：	1
17	Diethylanilineborane : a practical, safe, and consistent-quality borane source for the large-scale enantioselective reduction of a ketone intermediate in the synthesis of( R, R) -formoterol 显示文摘	WILKINSON H S TANOURY G J WALD S A	2002	Org Process Res Dev2002，6，2：	1
18	Microwave-assisted synthesis of room-temperature ionic liquid precursor in closed vessel 显示文摘	KHADILKAR B M REBEIRO G L	2002	Org Process Res Dev2002，6，6：	1
19	A scaleable synthesis of Bay 43-9006:a potent raf kinase inhibitor for the treatment of cancer显示文摘	Bankston D Dumas J Natero R	2002	Org Process Res Dev2002，6，6：	1
20	Inhibition of the cobalt acetate/bromide-catalyzed hydrogen peroxide oxidation of 4-tert-butyltoluene 显示文摘	Amin A A Beattie J K	2003	Org Process Res Dev2003，7，6：	1

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