cheminform abstract: synthesis of functionalized optically active bicyclic and angularly fused...

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1997 indan derivatives indan derivatives Q 1050 37 - 130 Synthesis of Functionalized Optically Active Bicyclic and Angularly Fused Tricyclic Compounds from (l)-Menthone by Tin-Mediated Vinyl Radical Cyclization. Starting from l-menthone the derivatives (I) and (VI) can be prepared which are used to synthesize the l-menthone propargylderivative (IV) and the spiromenthone propargyl compound (X), respectively. Their tin- mediated radical cyclization leads to the functionalized optically active title compounds (V) and (XI), respectively, which can serve as precursor for the synthesis of triquinane derivatives. — (SHANMUGAM, P.; SRINIVASAN, R.; RAJAGOPALAN, K.; Tetrahedron 53 (1997) 17, 6085-6096; Dep. Org. Chem., Univ. Madras, Madras 600 025, India; EN) 1

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Page 1: ChemInform Abstract: Synthesis of Functionalized Optically Active Bicyclic and Angularly Fused Tricyclic Compounds from (l)-Menthone by Tin-Mediated Vinyl Radical Cyclization

1997 indan derivatives

indan derivativesQ 1050

37 - 130Synthesis of Functionalized Optically Active Bicyclic and AngularlyFused Tricyclic Compounds from (l)-Menthone by Tin-MediatedVinyl Radical Cyclization. — Starting from l-menthone the derivatives(I) and (VI) can be prepared which are used to synthesize the l-menthonepropargylderivative (IV) and the spiromenthone propargyl compound (X),respectively. Their tin- mediated radical cyclization leads to the functionalizedoptically active title compounds (V) and (XI), respectively, which can serve asprecursor for the synthesis of triquinane derivatives. — (SHANMUGAM, P.;SRINIVASAN, R.; RAJAGOPALAN, K.; Tetrahedron 53 (1997) 17, 6085-6096;Dep. Org. Chem., Univ. Madras, Madras 600 025, India; EN)

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