Volume 19, Issue 2
Heterocyclic Compounds
Full Access

ChemInform Abstract: Control by Pyridine Nitrogen of the Dual-Channeled Triplet-State Di-π- methane Photorearrangement of 5,8-Dihydro-5,8-methanoquinoline Systems.

L. A. PAQUETTE

L. A. PAQUETTE

Evans Chem. Lab., Ohio State Univ., Columbus, OH 43210, USA

Search for more papers by this author
L. D. BURKE

L. D. BURKE

Evans Chem. Lab., Ohio State Univ., Columbus, OH 43210, USA

Search for more papers by this author
T. IRIE

T. IRIE

Evans Chem. Lab., Ohio State Univ., Columbus, OH 43210, USA

Search for more papers by this author
H. TANIDA

H. TANIDA

Evans Chem. Lab., Ohio State Univ., Columbus, OH 43210, USA

Search for more papers by this author
First published: January 12, 1988

Abstract

The methanoquinolines (I) undergo di-π-methane photorearrangement, producing mixtures of the regioisomers (II) and (III).

ChemInform Abstract

The methanoquinolines (I) undergo di-π-methane photorearrangement, producing mixtures of the regioisomers (II) and (III). The influence of the substituents on the regioselectivity is discussed by means of frontier molecular orbital theory.

    The full text of this article hosted at iucr.org is unavailable due to technical difficulties.