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A boryl-migratory semipinacol rearrangement
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作者 Dong-Hang Tan Zhi-Hao Chen +4 位作者 Ling Yang Chang-Ting Li Fang-Hai Tu Qingjiang Li Honggen Wang 《Science China Chemistry》 SCIE EI CSCD 2022年第4期746-752,共7页
The semipinacol rearrangement is one of the classic yet useful synthetic tools in organic synthesis.However,semipinacol rearrangements involving heteroatom-migration are rare.Reported herein is a boryl-migratory semip... The semipinacol rearrangement is one of the classic yet useful synthetic tools in organic synthesis.However,semipinacol rearrangements involving heteroatom-migration are rare.Reported herein is a boryl-migratory semipinacol rearrangement of α-hydroxyallylboronates and α-hydroxypropargylboronates triggered by diverse halogen-,oxygen-,sulfur-and seleniumcontaining electrophiles.The protocol leads to a mild and facile access to organoborons bearing valuable functionalities.The σ(C-B)hyperconjugation is believed to be the key factor that leads to the observed exclusive chemoselectivity and enhanced reactivity.Synthetic utilities of the formed products were demonstrated. 展开更多
关键词 1 2-boryl migration HYPERCONJUGATION iterative cross-coupling organoborons semipinacol rearrangement sp3-B tetrasubstituted alkene
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