Arturo Bulbarela - Academia.edu (original) (raw)

Uploads

Papers by Arturo Bulbarela

Research paper thumbnail of Carbon-13 NMR study of aniline derivatives

Magnetic Resonance in Chemistry, 1986

... ARTURO BULBARELA, HUGO TLAHUEXT, HILDA ROSA MORALES, LAURA CUELLAR, GUILLERMO URIBE and ROSAL... more ... ARTURO BULBARELA, HUGO TLAHUEXT, HILDA ROSA MORALES, LAURA CUELLAR, GUILLERMO URIBE and ROSALINDA CONTRERAS (to whom ... a R=H b R = H, hydrochloride c R=CH(CH,), d R = CH(CH3),, hydrochloride e R=C,H,, f R = CaHrl, hydrochloride ...

Research paper thumbnail of New Synthesis of Dihydro- and Tetrahydro-1,5-benzodiazepines by Reductive Condensation of o-Phenylenediamine and Ketones in the Presence of Sodium Borohydride

HETEROCYCLES, 1986

Dihydro-and t e t r ; l h y d r o-b e n i o d i a z e p i n e s have been syn thesized from o-phe... more Dihydro-and t e t r ; l h y d r o-b e n i o d i a z e p i n e s have been syn thesized from o-phenylenediamine dihydrochloride and aliphatic ketones in the presence of sodium borohydride. This article describes a new synthesis of 1,5-benzodiazepine derivatives, and represents a useful extension of known preparative routes to these compounds.

Research paper thumbnail of Carbon-13 NMR study of aniline derivatives

Magnetic Resonance in Chemistry, 1986

... ARTURO BULBARELA, HUGO TLAHUEXT, HILDA ROSA MORALES, LAURA CUELLAR, GUILLERMO URIBE and ROSAL... more ... ARTURO BULBARELA, HUGO TLAHUEXT, HILDA ROSA MORALES, LAURA CUELLAR, GUILLERMO URIBE and ROSALINDA CONTRERAS (to whom ... a R=H b R = H, hydrochloride c R=CH(CH,), d R = CH(CH3),, hydrochloride e R=C,H,, f R = CaHrl, hydrochloride ...

Research paper thumbnail of New Synthesis of Dihydro- and Tetrahydro-1,5-benzodiazepines by Reductive Condensation of o-Phenylenediamine and Ketones in the Presence of Sodium Borohydride

HETEROCYCLES, 1986

Dihydro-and t e t r ; l h y d r o-b e n i o d i a z e p i n e s have been syn thesized from o-phe... more Dihydro-and t e t r ; l h y d r o-b e n i o d i a z e p i n e s have been syn thesized from o-phenylenediamine dihydrochloride and aliphatic ketones in the presence of sodium borohydride. This article describes a new synthesis of 1,5-benzodiazepine derivatives, and represents a useful extension of known preparative routes to these compounds.