Aldol condensation reactions of (Dienone) tricarbonyliron complexes. 4. Enantioselective total synthesis of 3-deoxypentoses from (-)-myrtenal

Tetrahedron Letters

Volumn 38, Issue 25, 1997, Pages 4477-4478

  Franck Neumann, Michel ^a   Bissinger, Paul ^a   Geoffroy, Philippe ^a  

^a CNRS   (France)

Author keywords

[No Author keywords available]

Indexed keywords

MONOSACCHARIDE;

ARTICLE; DRUG SYNTHESIS; ENANTIOMER; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; POLYMERIZATION; REACTION ANALYSIS; STEREOCHEMISTRY;

EID: 0030994473     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(97)00906-4     Document Type: Article

References (8)

1. Franck-Neumann, M.; Bissinger, P.; Geoffroy, P. Tetrahedron Lett. 1997, communication before and ref. therein.
2. Salzer, A.; Schmalle, H.; Stauber, R.; Streiff, S. J. Organomet. Chem. 1991, 408, 403.
3. 8.
4. Reetz, M.T.; Raguse, B.; Marth, C.F.; Hügel, H.M.; Bach, T.; Fox, D.N.A. Tetrahedron 1992, 48, 5731.
5. Marshall, J.A.; Trometer, J.D.; Blough, B.E.; Crute, T.D. J. Org. Chem. 1988, 53, 4274.
6. Rychnovsky, S.D.; Rogers, B.; Yang, G. J. Org. Chem. 1993, 58, 3511.
7. 6, 200 MHz, PPm/TMS, Hz) : δ = 1.67 (s, 3H), 1.72 (s, 3H), 1.56-2.08 (m, 2H), 3.22 (dd, 2H, J = 5.2 and 0.9), 4.18 (d, 1H, J = 12.1), 4.25 (d, 1H, J = 12.1), 5.05 (dd, 1H, J = 10.7 and 3.5), 5.26 (m, 1H), 7.04-7.21 (m, 5H, arom), 9.06 (s, 1H).
8. Cupas, C; Roush, W.S. J. Org. Chem. 1969, 34, 742.