The solvent promoted addition of tetraallyltin to aldehydes: A convenient and chemoselective allylation procedure

Tetrahedron Letters

Volumn 37, Issue 11, 1996, Pages 1905-1908

  Cokley, Teresa M ^a   Marshall, Raymond L ^a   McCluskey, Adam ^a   Young, David J ^a  

^a GRIFFITH UNIVERSITY   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ALLYL COMPOUND;

ARTICLE; DRUG SYNTHESIS; NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS;

STAPHYLOCOCCUS PHAGE 3A;

EID: 0029917807     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(96)00149-9     Document Type: Article

References (11)

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2. Yanagisawa, A.; Inoue, H.; Morodome, M.; Yamamoto, H. J. Am. Chem. Soc. 1993, 115, 10356.
3. 4) and concentrated in vacuo. The crude product (3) was purified by kugel rohr distillation or filtration through a short bed of silica gel (dichloromethane).
4. For an example of the increased reactivity resulting from substitution of an electron withdrawing group on tin, see: Gambaro, A.; Ganis, P.; Marton, D.; Peruzzo, V.; Tagliavini, G. J. Organomet. Chem. 1982, 231, 307.
5. Hurd, C. D. J. Chem. Ed. 1966, 43, 527.
6. (a) Mulzer, J.; Angermann, A. Tetrahedron Lett. 1983, 24, 2843.
7. (b) Roush, W. R.; Walts, A. E.; Hoong, L. K. J. Am. Chem. Soc. 1985, 107, 8186.
8. (a) Young, D.; Kitching, W. Silicon, Germanium, Tin and Lead Compounds 1986, 9, 67.
9. (b) Lequan, M. M.; Guillerm, G. C. R. Hebd. Seances Acad. Sci. Ser. C. 1969, 268, 858.
10. (c) Verdone, J. A.; Margravite, J. A.; Scarpa, N. M.; Kuivila, H. G. J. Am. Chem. Soc. 1975, 97, 843.
11. (d) Beletskaya, I. P.; Kashin, A. N.; Reutov, O. A. J. Organomet. Chem. 1978, 155, 31.