ChemInform Abstract: SYNTHESES OF AZAPOLYCYCLIC COMPOUNDS BY AMINIUM RADICAL ROUTES: TRAPPING OF THE RADICAL INTERMEDIATES

Perry, R. A.; Lockhart, Robert W.; Kitadani, Masayuki; Chow, Yuan L.

doi:10.1002/chin.197908132

Chemischer Informationsdienst

1979

DOI: 10.1002/chin.197908132

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ChemInform Abstract: SYNTHESES OF AZAPOLYCYCLIC COMPOUNDS BY AMINIUM RADICAL ROUTES: TRAPPING OF THE RADICAL INTERMEDIATES

R. A. Perry¹,

Robert W. Lockhart²,

Masayuki Kitadani³

et al.

Abstract: Photolyse des Nitrosamins (I) in MeOH/HCl liefert das end Nitrat (IIb) (15% Ausb.), den exo‐Alkohol (IIc) (20%) und das Keton (III) (31%); in geringer Menge entsteht auch der endo‐Alkohol (IIa).

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ChemInform Abstract: SYNTHESES OF AZAPOLYCYCLIC COMPOUNDS BY AMINIUM RADICAL ROUTES: TRAPPING OF THE RADICAL INTERMEDIATES

Abstract: Photolyse des Nitrosamins (I) in MeOH/HCl liefert das end Nitrat (IIb) (15% Ausb.), den exo‐Alkohol (IIc) (20%) und das Keton (III) (31%); in geringer Menge entsteht auch der endo‐Alkohol (IIa).

Cited by 0 publications

References 1 publication

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