The first chemo- and regiospecific palladium-catalyzed enyne-diyne [4+2] intermolecular cross-benzannulation: An effective route to polysubstituted benzenes

Tetrahedron Letters

Volumn 38, Issue 49, 1997, Pages 8603-8604

  Gevorgyan, Vladimir ^a   Sadayori, Naoki ^a   Yamamoto, Yoshinori ^a  

^a TOHOKU UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

BENZENE DERIVATIVE;

ARTICLE; CATALYST; CHEMICAL MODIFICATION; CHEMICAL REACTION; REACTION ANALYSIS;

EID: 0030721031     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(97)10295-7     Document Type: Article

References (6)

1. Saito, S.; Salter, M. M.; Gevorgyan, V.; Tsuboya, N.; Tando, K.; Yamamoto, Y. J. Am. Chem. Soc. 1996, 118, 3970.
2. Gevorgyan, V.; Takeda, A.; Yamamoto, Y. J. Am. Chem. Soc. 1997, in press.
3. 5 intramolecular enyne-yne [4+2] cycloaddition reaction were recently reported.
4. Danheiser, R. L.; Gould, A. E.; Fernandez, de la Predilla, R.; Helgason, A. L. J. Org. Chem. 1994, 59, 5514.
5. Burrell, R. C.; Daoust, K. J.; Bradley, A. Z.; DiRico, K. J.; Johnson, R. P. J. Am. Chem. Soc. 1996, 118, 4218.
6. Gevorgyan, V.; Tando, K.; Uchiyama, N.; Yamamoto, Y. Unpublished results.