메뉴 건너뛰기




Volumn 20, Issue 3-4, 2008, Pages 282-287

Partial resolution of racemic trans-4-[5-(4-alkoxyphenyl)-2,5- dimethylpyrrolidine-1-oxyl-2-yl]benzoic acids by the diastereomer method with (R)- or (S)-1-phenylethylamine

Author keywords

1 phenylethylamine; Chiral amine; Chiral nitroxide; Crystal structure; Diastereomer method; Diastereomeric salt; Optical resolution; Racemic compound; Resolving agent

Indexed keywords

ALPHA METHYLBENZYLAMINE; BENZOIC ACID DERIVATIVE;

EID: 39749134848     PISSN: 08990042     EISSN: 1520636X     Source Type: Journal    
DOI: 10.1002/chir.20429     Document Type: Article
Times cited : (8)

References (16)
  • 1
    • 0002914584 scopus 로고    scopus 로고
    • Liquid crystalline radicals: An emerging class of organic magnetic materials
    • Lahti PM, editor, New York: Marcel Dekker;
    • Kaszynski P. Liquid crystalline radicals: an emerging class of organic magnetic materials. In: Lahti PM, editor. Magnetic properties of organic materials. New York: Marcel Dekker; 1999. p 305-324.
    • (1999) Magnetic properties of organic materials , pp. 305-324
    • Kaszynski, P.1
  • 2
    • 0003013115 scopus 로고    scopus 로고
    • Magnetic properties of transition-metal-containing liquid crystals
    • Lahti PM, editor, New York: Marcel Dekker;
    • Griesar K, Haase W. Magnetic properties of transition-metal-containing liquid crystals. In: Lahti PM, editor. Magnetic properties of organic materials. New York: Marcel Dekker; 1999. p 325-344.
    • (1999) Magnetic properties of organic materials , pp. 325-344
    • Griesar, K.1    Haase, W.2
  • 3
    • 4644292760 scopus 로고    scopus 로고
    • Magnetic properties of all-organic liquid crystals containing a chiral five-membered cyclic nitroxide unit within the rigid core
    • Ikuma N, Tamura R, Shimono S, Kawame N, Tamada O, Sakai N, Yamauchi J, Yamamoto Y. Magnetic properties of all-organic liquid crystals containing a chiral five-membered cyclic nitroxide unit within the rigid core. Angew Chem Int Ed 2004;43:3677-3682.
    • (2004) Angew Chem Int Ed , vol.43 , pp. 3677-3682
    • Ikuma, N.1    Tamura, R.2    Shimono, S.3    Kawame, N.4    Tamada, O.5    Sakai, N.6    Yamauchi, J.7    Yamamoto, Y.8
  • 6
    • 0001873427 scopus 로고
    • Cycloaddition of unsymmetrical olefins to the 1-pyrroline 1-oxides
    • Delpierre GR, Lamchen M, Nitrone. Part I. Cycloaddition of unsymmetrical olefins to the 1-pyrroline 1-oxides. J Chem Soc 1963;4693-4701.
    • (1963) J Chem Soc , pp. 4693-4701
    • Delpierre, G.R.1    Lamchen, M.2    Nitrone3    Part, I.4
  • 7
    • 0141618312 scopus 로고    scopus 로고
    • Synthesis of 2,2- and 2,5-disubstituted 1-oxy pyrrolidine radicals as new homobifunctional cross-linking spin labels
    • Kálai T, Jeko J, Hubbell WL, Hideg K. Synthesis of 2,2- and 2,5-disubstituted 1-oxy pyrrolidine radicals as new homobifunctional cross-linking spin labels. Synthesis 2003;2084-2088.
    • (2003) Synthesis , pp. 2084-2088
    • Kálai, T.1    Jeko, J.2    Hubbell, W.L.3    Hideg, K.4
  • 8
    • 0024590410 scopus 로고    scopus 로고
    • Short RP, Kennedy RM, Masamune S. An improved synthesis of (-)-(2R,5R)-dimethylpyrrolidine. J Org Chem 1989;54:1755-1756.
    • Short RP, Kennedy RM, Masamune S. An improved synthesis of (-)-(2R,5R)-dimethylpyrrolidine. J Org Chem 1989;54:1755-1756.
  • 9
    • 0000920450 scopus 로고
    • Complex induced proximity effects: Enantioselective syntheses based on asymmetric deprotonations of N-boc-pyrrolidines
    • Beak P, Kerrick ST, Wu S, Chu J. Complex induced proximity effects: enantioselective syntheses based on asymmetric deprotonations of N-boc-pyrrolidines. J Am Chem Soc 1994;116:3231-3239.
    • (1994) J Am Chem Soc , vol.116 , pp. 3231-3239
    • Beak, P.1    Kerrick, S.T.2    Wu, S.3    Chu, J.4
  • 10
    • 1642489270 scopus 로고    scopus 로고
    • Chiral discrimination during crystallization
    • Kinbara K, Saigo K. Chiral discrimination during crystallization. Top Stereochem 2003;23:207-265.
    • (2003) Top Stereochem , vol.23 , pp. 207-265
    • Kinbara, K.1    Saigo, K.2
  • 12
    • 33846650679 scopus 로고    scopus 로고
    • Dutch resolution of racemates and the roles of solid solution fromation and nucleation inhibition
    • Kellogg RM, Kaptein B, Vries TR. Dutch resolution of racemates and the roles of solid solution fromation and nucleation inhibition. Top Curr Chem 2007;269:159-157.
    • (2007) Top Curr Chem , vol.269 , pp. 159-157
    • Kellogg, R.M.1    Kaptein, B.2    Vries, T.R.3
  • 13
    • 33846652873 scopus 로고    scopus 로고
    • New resolution technologies controlled by chiral discrimination mechanisms
    • Sakai K, Sakurai R, Nohira H. New resolution technologies controlled by chiral discrimination mechanisms. Top Curr Chem 2007;269:199-231.
    • (2007) Top Curr Chem , vol.269 , pp. 199-231
    • Sakai, K.1    Sakurai, R.2    Nohira, H.3
  • 14
    • 33846676455 scopus 로고    scopus 로고
    • molecular mechanism of dielectrically controlled resolution (DCR)
    • Sakia K, Sakurai R, Hirayama N. molecular mechanism of dielectrically controlled resolution (DCR). Top Curr Chem 2007;269:233-271.
    • (2007) Top Curr Chem , vol.269 , pp. 233-271
    • Sakia, K.1    Sakurai, R.2    Hirayama, N.3
  • 15
    • 39749123031 scopus 로고    scopus 로고
    • Optical resolution by inclusion complexation with a chiral host compound
    • Toda F, editor, Dortrecht: Kluwer Academic Publishers;
    • Toda F. Optical resolution by inclusion complexation with a chiral host compound. In: Toda F, editor. Enantiomer separation: fundamentals and practical methods. Dortrecht: Kluwer Academic Publishers; 2004. p 1-47.
    • (2004) Enantiomer separation: Fundamentals and practical methods , pp. 1-47
    • Toda, F.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.