Synthesis of polysubstituted 3,4-dihydro-2-thiopyrans by regioselective annulation of 3,3-disubstituted allylic alcohols with a β-oxodithioester

Polyfunctionalized 3,4-dihydro-2 H -thiopyrans were obtained in high yields via the regioselective annulation of 3,3-disubstituted allylic alcohols with a β-oxodithioester under BF 3 ·Et 2 O catalysis. Polyfunctionalized 3,4-dihydro-2 H -thiopyrans were obtained in high yields via the regioselective...

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Veröffentlicht in:New journal of chemistry 2017-11, Vol.41 (22), p.13219-13221
Hauptverfasser: Kurva, Srinivas, Sriramoju, Vinodkumar, Madabhushi, Sridhar, Nanubolu, Jagadeesh Babu
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container_issue 22
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container_title New journal of chemistry
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creator Kurva, Srinivas
Sriramoju, Vinodkumar
Madabhushi, Sridhar
Nanubolu, Jagadeesh Babu
description Polyfunctionalized 3,4-dihydro-2 H -thiopyrans were obtained in high yields via the regioselective annulation of 3,3-disubstituted allylic alcohols with a β-oxodithioester under BF 3 ·Et 2 O catalysis. Polyfunctionalized 3,4-dihydro-2 H -thiopyrans were obtained in high yields via the regioselective annulation of 3,3-disubstituted allylic alcohols with a β-oxodithioester under BF 3 ·Et 2 O catalysis.
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title Synthesis of polysubstituted 3,4-dihydro-2-thiopyrans by regioselective annulation of 3,3-disubstituted allylic alcohols with a β-oxodithioester
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