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Catalytic Arylsulfonyl Radical Triggered 1,7-Enyne Bicyclizations
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文摘
A new metal-free bicyclization reaction of 1,7-enynes anchored by 伪,尾-conjugates with arylsulfonyl radicals generated in situ from sulfonyl hydrazides has been established using tert-butyl hydroperoxide and tetrabutylammonium iodide. The reactions occurred through sulfonylation/6-exo-dig/6-exo-trig bicyclization/in situ desulfonylation/5-exo-trig cyclization/alkyl or alkenyl migration cascade mechanism to give benzo[j]phenanthridines regioselectively.

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