Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Silvina C, Pellegrinet"'
Publikováno v:
The Journal of Organic Chemistry. 87:16776-16784
A DFT study of the Diels-Alder reactions of vinylboronic acid pinacol ester, allenylboronic acid pinacol ester, methyl acrylate, and methyl 2,3-butadienoate with cyclopentadiene has been performed. Competitive mechanisms for the reactions of the carb
Publikováno v:
European Journal of Organic Chemistry. 26
Publikováno v:
ARKIVOC, Vol 2011, Iss 7, Pp 343-357 (2011)
Externí odkaz:
https://doaj.org/article/cee4e87e1778467db513dcd4ab817527
Publikováno v:
Organic Letters. 24:8458-8458
Publikováno v:
ARKIVOC, Vol 2005, Iss 12, Pp 205-213 (2005)
Externí odkaz:
https://doaj.org/article/cf424884996f4a9ebdd4438d226caba8
Publikováno v:
ARKIVOC, Vol 2003, Iss 10, Pp 556-565 (2003)
Externí odkaz:
https://doaj.org/article/54e0350f253e458b811436089dda7392
Publikováno v:
European Journal of Organic Chemistry. 2019:2956-2970
Fil: Simonetti, Sebastian Osvaldo. Consejo Nacional de Investigaciones Cientificas y Tecnicas. Centro Cientifico Tecnologico Conicet - Rosario. Instituto de Quimica Rosario. Universidad Nacional de Rosario. Facultad de Ciencias Bioquimicas y Farmaceu
Publikováno v:
Organic letters. 23(13)
We have studied the reaction of allenylboronic acid pinacol ester with cyclopentadiene with experimental and computational methods. The reaction occurred efficiently with complete Diels-Alder periselectivity and regioselectivity at the proximal doubl
Publikováno v:
The Journal of organic chemistry. 85(11)
A DFT study of the mechanism of the Borono-Mannich reaction using benzylamine and piperidine as representative examples of primary and secondary amines with pinacol allenylboronate is presented. The study shows that both reactions progress through co
Theoretical Study of the BF3-Promoted Rearrangement of Oxiranyl N-Methyliminodiacetic Acid Boronates
Publikováno v:
The Journal of Organic Chemistry. 82:5917-5925
The mechanism of the rearrangement of oxiranyl N-methyliminodiacetyl (MIDA) boronates in dicholoromethane has been extensively investigated with density functional theory. Several reaction pathways were examined. Our results revealed that the most-fa