2013
DOI: 10.1002/anie.201209266
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Rhodium‐ and Platinum‐Catalyzed [4+3] Cycloaddition with Concomitant Indole Annulation: Synthesis of Cyclohepta[b]indoles

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Cited by 111 publications
(27 citation statements)
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“…Due to the convenience and efficiency in organic synthesis, tandem cyclizations have been studied with great depth in recent years. In 2013, a tandem cyclization to achieve cyclohepta[ b ]indoles was disclosed by Tang and his colleagues 8. In this report, the seven‐membered‐ring‐fused indole was synthesized involving a synchronous formation of indole.…”
Section: Methodsmentioning
confidence: 97%
“…Due to the convenience and efficiency in organic synthesis, tandem cyclizations have been studied with great depth in recent years. In 2013, a tandem cyclization to achieve cyclohepta[ b ]indoles was disclosed by Tang and his colleagues 8. In this report, the seven‐membered‐ring‐fused indole was synthesized involving a synchronous formation of indole.…”
Section: Methodsmentioning
confidence: 97%
“…[17] Cyclohepta[ b ]indole is present in a number of natural products [18] and bioactive pharmaceutical agents. [19] …”
mentioning
confidence: 99%
“…Briefly, we anticipated that the intramolecular cyclization [15] of the aniline derivative 1 would generate such an organometallic intermediate (A). At the heart of this design is the new strategy to generate a MÀC(sp 2 ) species capable of SiÀC bond activation, which is distinct from the previous transmetalation or oxidative insertion pathways (Scheme 1).…”
mentioning
confidence: 99%
“…At the heart of this design is the new strategy to generate a MÀC(sp 2 ) species capable of SiÀC bond activation, which is distinct from the previous transmetalation or oxidative insertion pathways (Scheme 1). Briefly, we anticipated that the intramolecular cyclization [15] of the aniline derivative 1 would generate such an organometallic intermediate (A). Subsequent selective activation of the SiÀC(sp 3 ) bond would provide the desired indole [3,2-b] silole 2.…”
mentioning
confidence: 99%