Condensation of all-E-retinal

Tetrahedron Letters

Volumn 38, Issue 30, 1997, Pages 5355-5358

  Verdegem, Peter J E ^a   Monnee, Menno C F ^a   Mulder, Patrick P J ^a   Lugtenburg, Johan ^a  

^a LEIDEN UNIVERSITY   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; BASE; RETINAL;

ARTICLE; MASS SPECTROMETRY; NUCLEAR MAGNETIC RESONANCE; POLYMERIZATION; REACTION ANALYSIS;

EID: 0030797301     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(97)01171-4     Document Type: Article

References (18)

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12. 20-nitrile is a common intermediate in vitamine-A synthesis; see e.g. ref. 10. IUPAC name: 9-(2,6,6-trimethyl-1-cyclohexenyl-1-yl)-3,7-dimethyl-2E,4E,6E,8E-nonatetraene nitrile.
13. max (n-hexane) 420 (C5-C15' chain) + 289 (C5'-C12' chain) nm.
14. March, J. Advanced Organic Chemistry : reactions, mechanisms, and structure; John Wiley & Sons: New York, 1992, pp. 937-944.
15. Duhamel, L.; Guillemont, J.; Poirier J. -M. Tet. Lett. 1991, 35, 4495-4498.
16. Thomas, A. F.; Guntz-Dubini, R. Helv. Chim. Acta 1976, 59, 2261-2267.
17. 15-aldehyde was prepared from β-ionone according to literature procedures, see e.g. Lugtenburg, J. Pure & Applied Chem. 1985, 57, 753-762.
18. max (n-hexane) 346 nm.