Multi-functionalized chiral crown ethers as enzyme models for the synthesis of peptides. Multiple chiral recognition in the enzyme model

Journal of Inclusion Phenomena and Macrocyclic Chemistry ◽

10.1007/bf01060727 ◽

1989 ◽

Vol 7 (2) ◽

pp. 267-276 ◽

Author(s):

Shigeki Sasaki ◽

Kenji Koga

Keyword(s):

Crown Ethers ◽

Chiral Recognition ◽

Enzyme Models ◽

Chiral Crown Ethers ◽

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Multi-Functionalized Chiral Crown Ethers as Enzyme Models for the Synthesis of Peptides. Multiple Chiral Recognition in the Enzyme Model

United States-Japan Seminar on Host-Guest Chemistry ◽

10.1007/978-94-009-0969-4_28 ◽

1989 ◽

pp. 267-276

Author(s):

Shigeki Sasaki ◽

Kenji Koga

Keyword(s):

Crown Ethers ◽

Chiral Recognition ◽

Enzyme Models ◽

Chiral Crown Ethers ◽

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Synthesis of Chiral Crown Ethers Derived fromtrans,trans-andcis,trans-2,2′-Spirobiindan-1,1′-diols. Their Chiral Recognition and Complexation Properties

Bulletin of the Chemical Society of Japan ◽

10.1246/bcsj.58.767 ◽

1985 ◽

Vol 58 (2) ◽

pp. 767-768 ◽

Author(s):

Koichiro Naemura ◽

Iwao Ebashi ◽

Masao Nakazaki

Keyword(s):

Crown Ethers ◽

Chiral Recognition ◽

Chiral Crown Ethers

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Synthesis of New Chiral Crown Ethers Incorporating Two Different Chiral Units and 'Matched/Mismatched' Effect of the Two Chiral Units on the Chiral Recognition

Bulletin of the Korean Chemical Society ◽

10.5012/bkcs.2007.28.12.2531 ◽

2007 ◽

Vol 28 (12) ◽

pp. 2531-2534 ◽

Keyword(s):

Crown Ethers ◽

Chiral Recognition ◽

Chiral Crown Ethers

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Synthesis of new chiral crown ethers containing a (p-methoxyphenoxy)methyl moiety and their chiral recognition ability towards amino acid esters

Tetrahedron Asymmetry ◽

10.1016/j.tetasy.2005.05.019 ◽

2005 ◽

Vol 16 (12) ◽

pp. 2119-2124 ◽

Author(s):

Mehmet Karakaplan ◽

Tarik Aral

Keyword(s):

Crown Ethers ◽

Chiral Recognition ◽

Amino Acid Esters ◽

Chiral Crown Ethers ◽

Recognition Ability ◽

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Biomimetic studies using artificial systems. II. Enantioselective thiolysis of D- or L-.ALPHA.-amino acid ester salts by thiol-bearing chiral crown ethers as an enzyme model.

Chemical and Pharmaceutical Bulletin ◽

10.1248/cpb.33.4247 ◽

1985 ◽

Vol 33 (10) ◽

pp. 4247-4266 ◽

Author(s):

SHIGEKI SASAKI ◽

MOTOJI KAWASAKI ◽

KENJI KOGA

Keyword(s):

Crown Ethers ◽

Amino Acid Ester ◽

Chiral Crown Ethers ◽

Enzyme Model ◽

Alpha Amino Acid

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ChemInform Abstract: Biomimetric Studies Using Artificial Systems. Part 2. Enantioselective Thiolysis of D- or L-a-Amino Acid Ester Salts by Thiol-Bearing Chiral Crown Ethers as an Enzyme Model.

Chemischer Informationsdienst ◽

10.1002/chin.198616328 ◽

1986 ◽

Vol 17 (16) ◽

Author(s):

S. SASAKI ◽

M. KAWASAKI ◽

K. KOGA

Keyword(s):

Crown Ethers ◽

Amino Acid Ester ◽

Chiral Crown Ethers ◽

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ChemInform Abstract: SYNTHESIS OF CHIRAL CROWN ETHERS DERIVED FROM TRANS,TRANS- AND CIS,TRANS-2,2′-SPIROBIINDAN-1,1′-DIOLS. THEIR CHIRAL RECOGNITION AND COMPLEXATION PROPERTIES

Chemischer Informationsdienst ◽

10.1002/chin.198532243 ◽

1985 ◽

Vol 16 (32) ◽

Author(s):

K. NAEMURA ◽

I. EBASHI ◽

M. NAKAZAKI

Keyword(s):

Crown Ethers ◽

Chiral Recognition ◽

Chiral Crown Ethers

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ChemInform Abstract: Synthesis of Chiral Crown Ethers Having Bromoarylene Moieties on Their Rim. Anomalous Behavior of Racemic Substrates in Cyclization to Crown Ethers.

10.1002/chin.199704187 ◽

2010 ◽

Vol 28 (4) ◽

pp. no-no

Author(s):

S. KIYOOKA ◽

M. TADA ◽

S. KAN ◽

M. FUJIO

Keyword(s):

Crown Ethers ◽

Anomalous Behavior ◽

Chiral Crown Ethers

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Measurement of Chiral Recognition Properties of Crown Ethers Using Matrix Assisted Laser Desorption Ionization Mass Spectrometry.

Journal of the Mass Spectrometry Society of Japan ◽

10.5702/massspec.48.141 ◽

2000 ◽

Vol 48 (2) ◽

pp. 141-144 ◽

Author(s):

Masami SAWADA ◽

Manabu HARADA ◽

Yoshio TAKAI ◽

Kazurou NAKANO ◽

Masao KURODA ◽

...

Keyword(s):

Mass Spectrometry ◽

Crown Ethers ◽

Chiral Recognition ◽

Laser Desorption ◽

Ionization Mass Spectrometry ◽

Ionization Mass ◽

Laser Desorption Ionization ◽

Desorption Ionization ◽

Matrix Assisted Laser ◽

Matrix Assisted Laser Desorption

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ChemInform Abstract: STUDIES ON THE OCCURRENCE OF HYDROGEN TRANSFER, 49. ON THE OPTICAL INDUCTION PRODUCED IN THE ELECTROREDUCTION OF ACETOPHENONE USING CHIRAL EPHEDRINE DERIVATIVES OR CHIRAL CROWN ETHERS AS SUPPORTING ELECTROLYTES

Chemischer Informationsdienst ◽

10.1002/chin.197815071 ◽

1978 ◽

Vol 9 (15) ◽

Author(s):

L. HORNER ◽

W. BRICH

Keyword(s):

Crown Ethers ◽

Hydrogen Transfer ◽

Chiral Crown Ethers ◽

Optical Induction ◽

Ephedrine Derivatives

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