113575-53-4Relevant academic research and scientific papers
PHOTOCYCLIZATION OF ENAMIDES. 37. SYNTHESIS OF DESPYRROLO ANALOGUES OF RESERPINE DEMONSTRATING A VERSATILE ADDITION-ELIMINATION REACTION STRATEGY FOR THE PREPARATION OF FUNCTIONALIZED RESERPINE RING SYSTEM
Naito, Takeaki,Kuroda, Etsuko,Miyata, Okiko,Ninomiya, Ichiya
, p. 1783 - 1801 (2007/10/02)
Despyrrolo analogues (25) and (26) of reserpine and were prepared via the routes involving reductive photocyclization of the enamide (4) and addition-elimination reaction of the resulting β-methoxy enones (7) and (8).
SYNTHESIS OF DEPYRROLO ANALOGUE OF RESERPINE
Miyata, Okiko,Doi, Etsuko,Naito, Takeaki,Ninomiya, Ichiya
, p. 1779 - 1782 (2007/10/02)
Depyrrolo analogue (19) of reserpine was synthesized via the route involving hydrocyanation reaction of the β-methoxyenone (7) followed by the Michael reaction of the α,β-unsaturated nitrile (11) with sodium methoxide.
