Unraveling innate substrate-controlled arylation and bicyclization of 1,5-enynes with α,β conjugates: synthesis of substituted benzo[a]fluorenes | Zendy

Babasaheb Sopan Gore | Zendy; Junhao Lin | Zendy; JehJeng Wang | Zendy

Open Access

Unraveling innate substrate-controlled arylation and bicyclization of 1,5-enynes with α,β conjugates: synthesis of substituted benzo[a]fluorenes

Author(s) -

Babasaheb Sopan Gore,

Junhao Lin,

JehJeng Wang

Publication year - 2021

Publication title -

green chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 2.221

H-Index - 221

eISSN - 1463-9270

pISSN - 1463-9262

DOI - 10.1039/d1gc01248g

Subject(s) - conjugate , substrate (aquarium) , chemistry , catalysis , combinatorial chemistry , substrate specificity , solvent , surface modification , brønsted–lowry acid–base theory , organic chemistry , enzyme , biology , mathematical analysis , ecology , mathematics

Herein, we describe a novel strategy for the aromatic C–H functionalization of electron-rich arenes with 1,5-enynes anchored by conjugates, catalyzed by a Brønsted acid under metal- and solvent-free conditions.

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