Issue 0, 1968

Nuclear magnetic resonance study of tricrotonylidenetetramine (1,2,3,3a,4,5,6,6a,7,8,9,9a-dodecahydro-2,5,8-trimethyl-1,4,7,96-tetra-azaphenalene)

Abstract

The less soluble isomer of 1,2,3,3a,4,5,6,6a,7,8,9,9a-dodecahydro-2,5,8-trimethyl-1,4,7,96-tetra-azaphenalene has trans-fused rings in chair forms with all methyl groups in equatorial positions. The more soluble isomer has one methyl group in an axial position.

Article information

Article type
Paper

J. Chem. Soc. B, 1968, 760-762

Nuclear magnetic resonance study of tricrotonylidenetetramine (1,2,3,3a,4,5,6,6a,7,8,9,9a-dodecahydro-2,5,8-trimethyl-1,4,7,96-tetra-azaphenalene)

K. G. R. Pachler and J. R. Parrish, J. Chem. Soc. B, 1968, 760 DOI: 10.1039/J29680000760

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