ChemInform Abstract: Stereoselectivity of Cyclizations via N-Acyliminium Ions to Form Pyrido[2′,3′:3,4]pyrrolo[2,1-a]isoindole, -isoquinoline and -benz[c]azepine Ring Systems.

MLA

Bahajaj, Abood A., et al. “ChemInform Abstract: Stereoselectivity of Cyclizations via N-Acyliminium Ions to Form Pyrido[2′,3′:3,4]Pyrrolo[2,1-a]Isoindole, -Isoquinoline and -Benz[c]Azepine Ring Systems.” ChemInform, vol. 32, no. 43, Oct. 2001, p. no. EBSCOhost, https://doi.org/10.1002/chin.200143027.

APA

Bahajaj, A. A., Vernon, J. M., & Wilson, G. D. (2001). ChemInform Abstract: Stereoselectivity of Cyclizations via N-Acyliminium Ions to Form Pyrido[2′,3′:3,4]pyrrolo[2,1-a]isoindole, -isoquinoline and -benz[c]azepine Ring Systems. ChemInform, 32(43), no. https://doi.org/10.1002/chin.200143027

Chicago

Bahajaj, Abood A., John M. Vernon, and Giles D. Wilson. 2001. “ChemInform Abstract: Stereoselectivity of Cyclizations via N-Acyliminium Ions to Form Pyrido[2′,3′:3,4]Pyrrolo[2,1-a]Isoindole, -Isoquinoline and -Benz[c]Azepine Ring Systems.” ChemInform 32 (43): no. doi:10.1002/chin.200143027.