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Volumn 68, Issue 9, 2003, Pages 3634-3639

Synthesis of p-tert-butylcalix[4]arene derivatives with trans-alkyl substituents on opposite methylene bridges

Author keywords

[No Author keywords available]

Indexed keywords

DOUBLE BONDS;

EID: 0037414567     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo026893q     Document Type: Article
Times cited : (25)

References (35)
  • 2
    • 0002577946 scopus 로고
    • (a) Böhmer, V. Angew. Chem., Int. Ed. Engl. 1995, 34, 713. Gutsche, C. D. Aldrichim. Acta 1995, 28, 1.
    • (1995) Aldrichim Acta , vol.28 , pp. 1
    • Gutsche, C.D.1
  • 3
    • 0004268367 scopus 로고    scopus 로고
    • Royal Society of Chemistry, Cambridge
    • (b) Gutsche, C. D. Calixarenes Revisited; Royal Society of Chemistry: Cambridge, 1998.
    • (1998) Calixarenes Revisited
    • Gutsche, C.D.1
  • 4
    • 0003773224 scopus 로고    scopus 로고
    • Asfari Z Böhmer V Harrowfield J Vicens J Eds Kluwer Academic Publishers Dordrecht
    • (c) For very recent reviews on calixarenes, see: Calixarenes 2001; Asfari, Z., Böhmer, V., Harrowfield, J., Vicens, J., Eds.; Kluwer Academic Publishers: Dordrecht, 2001.
    • (2001) Calixarenes
  • 9
    • 33748822682 scopus 로고    scopus 로고
    • For a review on the synthesis of calixarenes via the stepwise and fragment condensation methods, see: Böhmer, V. Liebigs Ann. / Recueil 1997, 2019.
    • (1997) Liebigs Ann./Recueil , pp. 2019
    • Böhmer, V.1
  • 22
    • 0000717550 scopus 로고    scopus 로고
    • For reviews on spirodienone calixarene derivatives, see: (a) Aleksiuk, O.; Grynszpan, F.; Litwak, M. A.; Biali, S. E. New J. Chem. 1996, 20, 473. (b) Biali, S. E. In ref 1c, pp 266-279. (c) Biali, S. E. Synlett 2003, 1-11.
    • (1996) New J. Chem. , vol.20 , pp. 473
    • Aleksiuk, O.1    Grynszpan, F.2    Litwak, M.A.3    Biali, S.E.4
  • 23
    • 0000717550 scopus 로고    scopus 로고
    • In ref 1c, pp 266-279
    • For reviews on spirodienone calixarene derivatives, see: (a) Aleksiuk, O.; Grynszpan, F.; Litwak, M. A.; Biali, S. E. New J. Chem. 1996, 20, 473. (b) Biali, S. E. In ref 1c, pp 266-279. (c) Biali, S. E. Synlett 2003, 1-11.
    • Biali, S.E.1
  • 24
    • 0037244554 scopus 로고    scopus 로고
    • For reviews on spirodienone calixarene derivatives, see: (a) Aleksiuk, O.; Grynszpan, F.; Litwak, M. A.; Biali, S. E. New J. Chem. 1996, 20, 473. (b) Biali, S. E. In ref 1c, pp 266-279. (c) Biali, S. E. Synlett 2003, 1-11.
    • (2003) Synlett. , pp. 1-11
    • Biali, S.E.1
  • 28
    • 0037077021 scopus 로고    scopus 로고
    • For the analysis of this pattern, see: Hoye, T. R.; Zhao, H. J. Org. Chem. 2002, 67, 4014.
    • (2002) J. Org. Chem. , vol.67 , pp. 4014
    • Hoye, T.R.1    Zhao, H.2
  • 29
    • 0242597888 scopus 로고    scopus 로고
    • note
    • 2O.
  • 31
    • 0000020584 scopus 로고
    • It seems likely that the reduction proceeds via a electron-transfer pathway. See, for example: Berz, S. H.; Dabbagh, G.; Mujsce, A. M. J. Am. Chern. Soc. 1991, 113, 631. For a review on the structure and reaction mechanisms of organocopper reagents, see: Nakamura, E.; Mori, S. Angew. Chern., Int. Ed. 2000, 39, 3751.
    • (1991) J. Am. Chern. Soc. , vol.113 , pp. 631
    • Berz, S.H.1    Dabbagh, G.2    Mujsce, A.M.3
  • 32
    • 0000283131 scopus 로고    scopus 로고
    • It seems likely that the reduction proceeds via a electron-transfer pathway. See, for example: Berz, S. H.; Dabbagh, G.; Mujsce, A. M. J. Am. Chern. Soc. 1991, 113, 631. For a review on the structure and reaction mechanisms of organocopper reagents, see: Nakamura, E.; Mori, S. Angew. Chern., Int. Ed. 2000, 39, 3751.
    • (2000) Angew Chern., Int. Ed. , vol.39 , pp. 3751
    • Nakamura, E.1    Mori, S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.