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Volumn 2002, Issue 10, 2002, Pages 72-79

Atropisomerism in some N,N′-diaryl-2-iminothiazoline derivatives: Chiral separation and configurational stability

Author keywords

Atropisomerism; Chiral HPLC; Enantiomerization barrier

Indexed keywords

2 IMINOTHIAZOLINE DERIVATIVE; ALPHA CHLOROACETONE; KETONE DERIVATIVE; N (2 METHOXYPHENYL) N [4 METHYL 3 (2 METHYLPHENYL) 1,3 THIAZOL 2 (3H) YLIDENE]AMINE; N (2 METHOXYPHENYL) N' (2 METHYLPHENYL)THIOUREA; N [3 (2 METHOXYPHENYL) 4 METHYL 1,3 THIAZOL 2(3H) YLIDENE] N (2 METHYLPHENYL)AMINE; THIAZOLE DERIVATIVE; THIOUREA DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0037854865     PISSN: 14246376     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (18)

References (20)
  • 3
    • 4143127565 scopus 로고    scopus 로고
    • The first examples of atropisomerism in a few N,N′-diaryl 2-iminothiazolines have been reported by some of us, without determination of the enantiomerization barriers, by a resolution of the enantiomers on cellulose triacetate stationary phase: Djafri, A.; Bouchekara, M.; Djafri, F.; Benachenhou, F. J. Soc. Alger. Chim., 1996, 6, 123-136.
    • (1996) J. Soc. Alger. Chim. , vol.6 , pp. 123-136
    • Djafri, A.1    Bouchekara, M.2    Djafri, F.3    Benachenhou, F.4
  • 4
    • 0010709414 scopus 로고
    • Ed.: Trost, Barry M.: Blackwell, Oxford, UK
    • For biaryl atropisomers: (a) Noyori, R. in Stereocontrolled Organic Synthesis, Ed.: Trost, Barry M. 1994, 1-15: Blackwell, Oxford, UK.
    • (1994) Stereocontrolled Organic Synthesis , pp. 1-15
    • Noyori, R.1
  • 7
    • 4143137379 scopus 로고    scopus 로고
    • Non-biaryl atropisomers: New classes of chiral reagents, auxiliaries and ligands?
    • Ed.: Schmalz, H.-G. Wiley-VCH Verlag GmbH, Weinheim, Germany
    • For non-biaryl atropisomers: (a) Clayden J. Non-biaryl Atropisomers: New Classes of Chiral Reagents, Auxiliaries and Ligands? Ed.: Schmalz, H.-G. Organic Synthesis Highlights IV, 2000, 48-52. Wiley-VCH Verlag GmbH, Weinheim, Germany.
    • (2000) Organic Synthesis Highlights IV , pp. 48-52
    • Clayden, J.1
  • 12
    • 4143147265 scopus 로고
    • Reference 1 gives examples of hydrolysis under severe conditions. We were not able to reproduce the results reported for non-ortho- substituted aryl iminothiazolines in: Sahu, B.; Dash, B. C.; Tripathy, H.; Mahapatra, G. N. Indian J. Appl. Chem. 1970, 33, 256-258.
    • (1970) Indian J. Appl. Chem. , vol.33 , pp. 256-258
    • Sahu, B.1    Dash, B.C.2    Tripathy, H.3    Mahapatra, G.N.4
  • 17
    • 4143138495 scopus 로고    scopus 로고
    • Viswanathan, K. V.; Raghavan, M.; Guha, P. C. J. Indian Inst. Sci. 1953, 35A, 251-258 (Chem. Abs., 48: 64,250).
    • Chem. Abs. , vol.48


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.