Abstract
The efficient syntheses of 6,6,8,6,6-pentacyclic naphtho-fused
oxazocinoquinolinones and 6,6,8,6,6,6-hexacyclic benzo[g ]quinoxalino-fused oxazocinoquinolinones
were achieved in one-pot sequences. The generation of libraries
of their diaryl- and alkynyl-substituted analogues via Suzuki-Miyaura
and Sonogashira cross-coupling reactions, respectively, were also
achieved.
Key words
fused-ring systems - oxazocinoquinolinones - diarylations - alkynylations - cross-coupling
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20 For the single-crystal X-ray crystallographic
analysis of compound 3a (C21 H15 NO2 ),
yellowish needle-shaped crystals were grown from CHCl3 -MeCN
(7:3); monoclinic, space group P 2(1)/n ; unit cell parameters: a = 14.102(5), b = 15.073(5), c = 15.994(6).
Diffraction data were measured with MoKα (0.71073 Å)
radiation at 296 K using a Kappa Apex 2 instrument. The structure
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² were carried out
against all reflections using SHELX-97.
21 For the single-crystal X-ray crystallographic
analysis of compound 11a (C25 H16 ClNO2 ),
yellowish block-shaped crystals were grown from CHCl3 -MeCN
(9:1); triclinic, space group P 1; unit
cell parameters: a = 9.1980(7), b = 10.0460(8), c = 10.9903(9), α = 70.913(3), β = 87.778(3), γ = 79.707(2).
Diffraction data were measured with MoKα (0.71073 Å)
radiation at 296 K using a Kappa Apex 2 instrument. The structure
was solved by direct methods using the SHELX-97 program. Refinements of F
² were carried out
against all reflections using SHELX-97.