ChemInform Abstract: Preparation of Optically Active Succinic Acid Derivatives. Part 1. Optical Resolution of 2-Benzyl-3-(cis-hexahydroisoindolin-2-ylcarbonyl)propionic Acid.

T. YAMAGUCHI; T. YANAGI; H. HOKARI; Y. MUKAIYAMA; T. KAMIJO; I. YAMAMOTO

doi:10.1002/chin.199812095

ChemInform Abstract: Preparation of Optically Active Succinic Acid Derivatives. Part 1. Optical Resolution of 2-Benzyl-3-(cis-hexahydroisoindolin-2-ylcarbonyl)propionic Acid.

ChemInform ◽

10.1002/chin.199812095 ◽

2010 ◽

Vol 29 (12) ◽

pp. no-no

Author(s):

T. YAMAGUCHI ◽

T. YANAGI ◽

H. HOKARI ◽

Y. MUKAIYAMA ◽

T. KAMIJO ◽

...

Keyword(s):

Succinic Acid ◽

Propionic Acid ◽

Optical Resolution ◽

Optically Active

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Preparation of Optically Active Succinic Acid Derivatives. I. Optical Resolution of 2-Benzyl-3-(cis-hexahydroisoindolin-2-ylcarbonyl)propionic Acid.

Chemical and Pharmaceutical Bulletin ◽

10.1248/cpb.45.1518 ◽

1997 ◽

Vol 45 (9) ◽

pp. 1518-1520 ◽

Cited By ~ 11

Author(s):

Toshiaki YAMAGUCHI ◽

Takashi YANAGI ◽

Hiroshi HOKARI ◽

Yuko MUKAIYAMA ◽

Tetsuhide KAMIJO ◽

...

Keyword(s):

Succinic Acid ◽

Propionic Acid ◽

Optical Resolution ◽

Optically Active

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Efficient co‐production of propionic acid and succinic acid by Propionibacterium acidipropionici using membrane separation coupled technology

Engineering in Life Sciences ◽

10.1002/elsc.202000103 ◽

2021 ◽

Vol 21 (6) ◽

pp. 429-437

Author(s):

Xiaolian Li ◽

Liquan Wei ◽

Ziqiang Wang ◽

Yunshan Wang ◽

Zhiguo Su

Keyword(s):

Succinic Acid ◽

Propionic Acid ◽

Membrane Separation ◽

Propionibacterium Acidipropionici

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Optically Active Triptycenes. VII. Synthesis, Optical Resolution and Absolute Configuration of 3-Chloro and 4-Chloro-7-substituted Triptycenes.

Bulletin of the Chemical Society of Japan ◽

10.1246/bcsj.47.1761 ◽

1974 ◽

Vol 47 (7) ◽

pp. 1761-1766 ◽

Cited By ~ 5

Author(s):

Michiaki Hashimoto ◽

Yasumi Shimizu ◽

Fumio Ogura ◽

Masazumi Nakagawa

Keyword(s):

Absolute Configuration ◽

Optical Resolution ◽

Optically Active

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ChemInform Abstract: Optically Active Aromatics Possessing Helical Chirality: One-Pot Synthesis, Optical Resolution and Crystal Structure of 13,14-Dimethyldibenzo[b,j][4,7]phenanthroline and Its Dihydro Form as a Novel Chiral Building Block.

ChemInform ◽

10.1002/chin.199850173 ◽

2010 ◽

Vol 29 (50) ◽

pp. no-no

Author(s):

Y. TANAKA ◽

A. SEKITA ◽

H. SUZUKI ◽

M. YAMASHITA ◽

T. OSHIKAWA ◽

...

Keyword(s):

Crystal Structure ◽

Building Block ◽

Optical Resolution ◽

Optically Active ◽

One Pot ◽

One Pot Synthesis ◽

Chiral Building Block ◽

Helical Chirality

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Preparation of optically active proline. Optical resolution of N-acyl-DL-proline by preferential crystallization procedure

Journal of Agricultural and Food Chemistry ◽

10.1021/jf60207a049 ◽

1976 ◽

Vol 24 (5) ◽

pp. 903-906 ◽

Cited By ~ 13

Author(s):

Chikara Hongo ◽

Masataka Shibazaki ◽

Shigeki Yamada ◽

Ichiro Chibata

Keyword(s):

Optical Resolution ◽

Optically Active ◽

Crystallization Procedure

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ChemInform Abstract: A New Chiral Host Compound 10,10′-Dihydroxy-9,9′-biphenanthryl. Optical Resolution of Propionic Acid Derivatives, Butyric Acid Derivatives, and 4-Hydroxycyclopent-2-en-1-one Derivatives by Complexation.

ChemInform ◽

10.1002/chin.198836350 ◽

1988 ◽

Vol 19 (36) ◽

Author(s):

F. TODA ◽

K. TANAKA

Keyword(s):

Propionic Acid ◽

Butyric Acid ◽

Optical Resolution ◽

Host Compound

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Efficient optical resolution of cis-4-methylcyclohex-4-ene-1,2-dicarboxylic anhydride, cis-4- methylcyclohex-4-ene-1,2-dicarboximide, and their derivatives by complexation with optically active host compounds derived from tartaric acid

Journal of the Chemical Society Perkin Transactions 1 ◽

10.1039/p19940001601 ◽

1994 ◽

pp. 1601 ◽

Cited By ~ 7

Author(s):

Fumio Toda ◽

Hisakazu Miyamoto ◽

Hiroyuki Ohta

Keyword(s):

Tartaric Acid ◽

Optical Resolution ◽

Optically Active

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CNS Agents: Optical Resolution with Baker's Yeast as Key Step in the Synthesis of Optically Active Tricyclic Amines

Heterocycles ◽

10.3987/com-93-6588 ◽

1994 ◽

Vol 38 (4) ◽

pp. 709 ◽

Cited By ~ 2

Author(s):

Bernhard W殤sch ◽

Heike Diekmann

Keyword(s):

Optical Resolution ◽

Optically Active ◽

Baker’S Yeast ◽

Baker's Yeast

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ChemInform Abstract: OPTICALLY ACTIVE TRIPTYCENES PART 7, SYNTHESIS, OPTICAL RESOLUTION AND ABSOLUTE CONFIGURATION OF 3-CHLORO AND 4-CHLORO-7-SUBSTITUTED TRIPTYCENES

Chemischer Informationsdienst ◽

10.1002/chin.197439250 ◽

1974 ◽

Vol 5 (39) ◽

pp. no-no

Author(s):

MICHIAKI HASHIMOTO ◽

YASUMI SHIMIZU ◽

FUMIO OGURA ◽

MASAZUMI NAKAGAWA

Keyword(s):

Absolute Configuration ◽

Optical Resolution ◽

Optically Active

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Synthesis and Characterization of Chiral Conducting Polymers Based on Polypyrrole

Australian Journal of Chemistry ◽

10.1071/c96189 ◽

1997 ◽

Vol 50 (9) ◽

pp. 939 ◽

Cited By ~ 7

Author(s):

Fang Chen ◽

Parveen Akhtar ◽

Leon A. P. Kane-Maguire ◽

Gordon G. Wallace

Keyword(s):

Conducting Polymers ◽

Propionic Acid ◽

Spectroscopic Properties ◽

Optically Active ◽

Synthesis And Characterization ◽

Chiroptical Properties ◽

Covalently Bonded ◽

Circular Dichroïsm ◽

Ring Position

A range of optically active pyrrole monomers have been synthesized in which a chiral sub- stituent is covalently bonded either to the pyrrole N or C3 ring position, namely (–)-(1R)-4-methyl-N-(1-phenylethyl)pyrrole-3-carboxamide, (+)-(1S)-4-methyl-N-(1-phenylethyl)pyrrole-3-carboxamide, (–)-(1R)-4-methyl-N-(1-naphthylethyl)pyrrole-3-carboxamide, (+)-(1S)-4-methyl-N-(1-naphthylethyl)pyrrole-3-carboxamide, (+)-(2S)-2-(1H-pyrrol-1-yl)propionic acid, (+)-(1S)-N-(1-phenyl-ethyl)pyrrole, and (–)-(1R)-N-(1-phenylethyl)pyrrole. Their chiroptical properties have been established by circular dichroism spectroscopy. Electropolymerization of the three N-substituted pyrrole monomers provided films of chiral conducting polymers, whose electrical and spectroscopic properties are described. Although oxidation of the C3 substituted pyrrole monomers was also facile, electrodeposition was poor and films of the associated polymers could not be obtained.

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