Highly stereoselective additions of cuprates to a polyfunctional enone

Tetrahedron Asymmetry

Volumn 8, Issue 10, 1997, Pages 1515-1518

  Amigoni, S ^a   Schulz, J ^a   Martin, L ^a   Le Floc'h, Y ^a  

^a CNRS ESA 6052   (France)

Author keywords

[No Author keywords available]

Indexed keywords

HETEROCYCLIC COMPOUND; LACTONE DERIVATIVE;

CHEMICAL MODIFICATION; DRUG SYNTHESIS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PRIORITY JOURNAL; REACTION ANALYSIS; SHORT SURVEY; STEREOCHEMISTRY;

EID: 0030914114     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(97)00148-1     Document Type: Article

References (11)

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3. Acker, R. D. Tetrahedron Lett. 1977, 3407-10; 1978, 2399-402.
4. Acker, R. D. Tetrahedron Lett. 1977, 3407-10; 1978, 2399-402.
5. Four, P.; Le Tri, P.; Riviere, H. J. Organomet. Chem. 1977, 136, 103-10.
6. Yamamoto, Y.; Nishii, S.; Ibuka, T. J. Chem. Soc., Chem. Commun. 1987, 464-6.
7. Yamamoto, Y.; Chouan, Y.; Nishii, S.; Ibuka, T.; Kitahara, H. J. Am. Chem. Soc. 1992, 114, 7652-60.
8. Dorigo, A. E.; Morokuma, K. J. Am. Chem. Soc. 1989, 111, 6524-36.
9. 3) δ: 19.2, 23.1, 26.9, 68.7, 127.7, 129.9, 133.2, 133.7, 135.7, 135.8, 160.5, 193.8.
10. Trahanovsky, W. S.; Macaulay, D. B. J. Org. Chem. 1973, 38, 1497-99.
11. 3) δ: 15.0, 15.1, 19.4, 21.5, 27.0, 39.4, 48.3, 62.9, 73.1, 102.6, 126.4-141.9, 205.2.