Study of cis/transand endo/exoDiastereoselectivity in the [4+3]-Cycloaddition Reaction of 2-Functionalized Furans and Dimethyloxyallyl Cation: Preparation of Versatile Cycloheptane Synthons

MLA

Montaña, Angel M., et al. “Study of Cis/Transand Endo/ExoDiastereoselectivity in the [4+3]-Cycloaddition Reaction of 2-Functionalized Furans and Dimethyloxyallyl Cation: Preparation of Versatile Cycloheptane Synthons.” Chemistry Letters, vol. 26, no. 9, Sept. 1997, pp. 847–48. EBSCOhost, https://doi.org/10.1246/cl.1997.847.

APA

Montaña, A. M., Ribes, S., Grima, P. M., & García, F. (1997). Study of cis/transand endo/exoDiastereoselectivity in the [4+3]-Cycloaddition Reaction of 2-Functionalized Furans and Dimethyloxyallyl Cation: Preparation of Versatile Cycloheptane Synthons. Chemistry Letters, 26(9), 847–848. https://doi.org/10.1246/cl.1997.847

Chicago

Montaña, Angel M, Sandra Ribes, Pedro M Grima, and Francisca García. 1997. “Study of Cis/Transand Endo/ExoDiastereoselectivity in the [4+3]-Cycloaddition Reaction of 2-Functionalized Furans and Dimethyloxyallyl Cation: Preparation of Versatile Cycloheptane Synthons.” Chemistry Letters 26 (9): 847–48. doi:10.1246/cl.1997.847.