JPH0333703B2 - - Google Patents

Info

Publication number
JPH0333703B2
JPH0333703B2 JP57043603A JP4360382A JPH0333703B2 JP H0333703 B2 JPH0333703 B2 JP H0333703B2 JP 57043603 A JP57043603 A JP 57043603A JP 4360382 A JP4360382 A JP 4360382A JP H0333703 B2 JPH0333703 B2 JP H0333703B2
Authority
JP
Japan
Prior art keywords
acid
group
naphthyl
mandelic acid
asymmetric
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP57043603A
Other languages
English (en)
Japanese (ja)
Other versions
JPS58159451A (ja
Inventor
Takafumi Ooi
Akira Doi
Hajime Kitahara
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo Chemical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP57043603A priority Critical patent/JPS58159451A/ja
Publication of JPS58159451A publication Critical patent/JPS58159451A/ja
Publication of JPH0333703B2 publication Critical patent/JPH0333703B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
JP57043603A 1982-03-17 1982-03-17 アミド誘導体およびそれを固定相とする鏡像体混合物のガスクロマトグラフイ−分析法 Granted JPS58159451A (ja)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57043603A JPS58159451A (ja) 1982-03-17 1982-03-17 アミド誘導体およびそれを固定相とする鏡像体混合物のガスクロマトグラフイ−分析法

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57043603A JPS58159451A (ja) 1982-03-17 1982-03-17 アミド誘導体およびそれを固定相とする鏡像体混合物のガスクロマトグラフイ−分析法

Publications (2)

Publication Number Publication Date
JPS58159451A JPS58159451A (ja) 1983-09-21
JPH0333703B2 true JPH0333703B2 (2) 1991-05-20

Family

ID=12668393

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57043603A Granted JPS58159451A (ja) 1982-03-17 1982-03-17 アミド誘導体およびそれを固定相とする鏡像体混合物のガスクロマトグラフイ−分析法

Country Status (1)

Country Link
JP (1) JPS58159451A (2)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103439457B (zh) * 2013-08-28 2015-07-08 南通天泽化工有限公司 一种40%dv菊酸含量测定方法

Also Published As

Publication number Publication date
JPS58159451A (ja) 1983-09-21

Similar Documents

Publication Publication Date Title
Ôi et al. Enantiomer separation by HPLC with some urea derivatives of L-valine as novel chiral stationary phases
Garner et al. A stereodivergent synthesis of D-erythro-sphingosine and D-threo-sphingosine from L-serine
Weinstein et al. N-acyl derivatives of chiral amines as novel, readily prepared phases for the separation of optical isomers by gas chromatography
US4604207A (en) Packing materials for chromatographic use and a method for analysis of an enantiomer mixture using the same
Raber et al. Esterification of carboxylic acids with trialkyloxonium salts
Tai et al. Stereochemical studies of the hydrogenation with asymmetrically modified nickel catalysts; the hydrogenation of methyl 2-alkyl-3-oxobutyrate.
US5412108A (en) Method for preparing 1,2,4-cyclohexanetricarboxylic acid and anhydride
JP2009507870A (ja) 4−置換ピロリジン−2−オン及びそれらの使用
Doolittle et al. (S)-Tetrahydro-5-oxo-2-furancarboxylic acid: a chiral derivatizing reagent for asymmetric alcohols
Takeuchi et al. Chemistry of novel compounds with multifunctional carbon structure. 9. Molecular design, synthetic studies, and NMR investigation of several efficient chiral derivatizing reagents which give very large 19F NMR. DELTA.. delta. values in enantiomeric excess determination
Bradshaw et al. Polysiloxanes containing thermally stable chiral amide side-chains for capillary gas and supercritical fluid chromatography
JPH0333703B2 (2)
EP0469739A1 (en) Stationary phase for enantiomeric resolution in liquid chromatography
Miyano et al. Use of axially chiral 2'-methoxy-1, 1'-binaphthyl-2-carboxylic acid as chiral derivatizing agent for discrimination of enantiomeric alcohols and amines by 1H NMR.
US5051176A (en) Packing material for liquid chromatography
US4487956A (en) Menthyl 2,2-dimethylcyclopropanecarboxylate and resolution of the same
Parr et al. N-trifluoroacetyl-l-norvalyl-l-norvaline cyclohexyl ester as a stationary phase and its interaction with asymmetric solutes
JPS6125698B2 (2)
JPH0153670B2 (2)
US5041573A (en) Optically active carboalkylated amino alcohols and their utilization in optical resolution
Harada et al. Asymmetric catalytic hydrogenations of chiral. ALPHA.-keto amides.
Gilbert et al. Characterization of diastereomeric and enantiomeric ephedrines by gas chromatography combined with electron impact mass spectrometry and isobutane chemical ionization mass spectrometry
JPH02223547A (ja) 環式共溶媒を使用する5‐シアノ吉草酸およびそれのエステル類の製造
Saigo et al. Optically active anti head-to-head coumarin dimer. A new agent for the determination of enantiomeric excess of amines and alcohols.
JP2912078B2 (ja) ガスクロマトグラフィー用光学活性カラム充填剤