Source: Journal of the Royal Society of Chemistry. Perkin Tansactions 2. Unidade: FFCLRP
Assunto: QUÍMICA
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LAALI, Kenneth K. et al. Superacid protonation of dihydrocyclobuta[e]pyrene and its 'C IND. 60'-o-quinodimethane adduct. An NMR, ab initio/GIAO and AMI/PM3 study. Journal of the Royal Society of Chemistry. Perkin Tansactions 2, n. 10, p. 2129-2132, 1999Tradução . . Acesso em: 04 maio 2024.APA
Laali, K. K., Hollenstein, S., Galembeck, S. E., Nakamura, Y., & Nishimura, J. (1999). Superacid protonation of dihydrocyclobuta[e]pyrene and its 'C IND. 60'-o-quinodimethane adduct. An NMR, ab initio/GIAO and AMI/PM3 study. Journal of the Royal Society of Chemistry. Perkin Tansactions 2, ( 10), 2129-2132.NLM
Laali KK, Hollenstein S, Galembeck SE, Nakamura Y, Nishimura J. Superacid protonation of dihydrocyclobuta[e]pyrene and its 'C IND. 60'-o-quinodimethane adduct. An NMR, ab initio/GIAO and AMI/PM3 study. Journal of the Royal Society of Chemistry. Perkin Tansactions 2. 1999 ;( 10): 2129-2132.[citado 2024 maio 04 ]Vancouver
Laali KK, Hollenstein S, Galembeck SE, Nakamura Y, Nishimura J. Superacid protonation of dihydrocyclobuta[e]pyrene and its 'C IND. 60'-o-quinodimethane adduct. An NMR, ab initio/GIAO and AMI/PM3 study. Journal of the Royal Society of Chemistry. Perkin Tansactions 2. 1999 ;( 10): 2129-2132.[citado 2024 maio 04 ]
