An approach to electronic communication through transannular hydrogen bond: Synthesis of cyclic diamines bearing donor and acceptor groups

Tetrahedron Letters

Volumn 37, Issue 27, 1996, Pages 4721-4724

  Schneider, Raoul ^a   Hosseini, Mir Wais ^a   Planeix, J M ^a  

^a UNIVERSITÉ DE STRASBOURG   (France)

Author keywords

[No Author keywords available]

Indexed keywords

DIAMINE; MACROCYCLIC COMPOUND;

ARTICLE; DRUG STRUCTURE; DRUG SYNTHESIS; REACTION ANALYSIS; X RAY CRYSTALLOGRAPHY;

EID: 0030199647     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(96)00966-5     Document Type: Article

References (18)

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9. 3); 100.0, 103.2, 121.5, 128.0, 129.4, 132.9, 133.8, 143.1, 155.3, 155.9 (Ar).
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11. 2O (3×20 ml) before it was evaporated to dryness leaving the desired compound 5 (106 mg, 81 % yield) as a slightly coloured solid. Compound 5 was used in the next step without further purification.
12. 3); 100.0, 103.4, 112.5, 122.3, 125.8, 134.3, 137.0, 155.2, 155.4, 156.4 (Ar).
13. 13 Pietra, F., Del Cima, F. J. Org. Chem., 1968, 33, 1411-1416.
14. 2); 127.8, 129.8, 133.3, 143.9 (Ts); 111.0, 126.0, 136.3, 153.8 (Ar).
15. 2); 111.6, 125.9, 136.8, 142.9, 154.5 (Ar).
16. 2); 110.9, 125.7, 137.1, 152.7 (Ar).
17. 3); 111.5, 120.4, 121.8, 140.8, 154.1 (Ar).
18. 18 ten Hoeve, W., Kruse, C. G., Luteyn, J. M., Thiecke, J. R. G., Wynberg, H. J. Org. Chem., 1993, 58, 5101-5106.