Structure dependent yield of the cyclization of outside-templated bisacetylenes: Catenation or oligomerization?

Tetrahedron Letters

Volumn 39, Issue 13, 1998, Pages 1735-1736

  Höger, Sigurd ^a   Meckenstock, Anne Désirée ^a  

^a MAX PLANCK INSTITUTE FOR POLYMER RESEARCH   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ACETYLENE DERIVATIVE; BISACETYLENE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL MODIFICATION; CHEMICAL STRUCTURE; CYCLIZATION; MOLECULAR DYNAMICS; OLIGOMERIZATION;

EID: 0032568351     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)00056-2     Document Type: Article

References (8)

1. 1) For recent articles dealing with template reactions see: a) S. Anderson, H.L. Anderson, J.K.M. Sanders, Acc. Chem. Res., 26, 469, (1993).
2. b) R. Hoss, F. Vögtle, Angew. Chem. Int. Ed. Engl., 33, 375 (1994);
3. c) B. Dietrich, P. Viout, J.-M. Lehn, Macrocyclic Chemistry, VCH, Weinheim, 1993. Chap. 3.3.
4. 2) D.W.J. McCallien, J.K.M. Sanders, J. Am. Chem. Soc., 117, 6611 (1995).
5. 3) S. Höger, A.-D. Meckenstock, H. Pellen, J. Org. Chem., 62, 4556 (1997).
6. 4) D. O'Krongly, S. R. Denmade, M. Y. Chiang, R. Breslow, J. Am. Chem. Soc., 107, 5544 (1985).
7. 8): 7.63-7.61 (m, 4 H), 7.60-7.58 (m, 4 H), 7.57-7-55 (m, 4 H), 7.29-7.27 (m, 2 H), 7.14 (s, 4 H), 7, 13 (s, 4 H), 7.07-7.05 (m, 4 H), 4.04 (t, J = 6.49 Hz, 4 H), 3.89 (s, 24 H), 3.51 (t, J = 6.11 Hz, 4 H), 3,37 (s, 2 H, OH), 1.90-1-75 (m, 4 H), 1.60-1.40 (m, 12 H), 1.36 (s, 36 H).
8. 6) G. Illuminati, L. Mandolini, Acc. Chem. Res., 14, 95, (1981).