Efficient synthesis of benzocyclotrimer analogues by Negishi cross-coupling and intramolecular nucleophilic substitution
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作者:
Borges-Gonzalez, Jorge
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CSIC, Inst Prod Nat & Agrobiol, Avda Astrofis Francisco Sanchez 3, San Cristobal la Laguna 38206, Sc De Tenerife, SpainCSIC, Inst Prod Nat & Agrobiol, Avda Astrofis Francisco Sanchez 3, San Cristobal la Laguna 38206, Sc De Tenerife, Spain
Borges-Gonzalez, Jorge
[1
]
Martin, Tomas
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CSIC, Inst Prod Nat & Agrobiol, Avda Astrofis Francisco Sanchez 3, San Cristobal la Laguna 38206, Sc De Tenerife, Spain
Inst Univ Bioorgan Antonio Gonzalez, CIBICAN, Avda Astrofis Francisco Sanchez 2, San Cristobal la Laguna 38206, Sc De Tenerife, SpainCSIC, Inst Prod Nat & Agrobiol, Avda Astrofis Francisco Sanchez 3, San Cristobal la Laguna 38206, Sc De Tenerife, Spain
Martin, Tomas
[1
,2
]
机构:
[1] CSIC, Inst Prod Nat & Agrobiol, Avda Astrofis Francisco Sanchez 3, San Cristobal la Laguna 38206, Sc De Tenerife, Spain
[2] Inst Univ Bioorgan Antonio Gonzalez, CIBICAN, Avda Astrofis Francisco Sanchez 2, San Cristobal la Laguna 38206, Sc De Tenerife, Spain
We report a new and efficient synthetic strategy that allows access to flexible and functionalized benzocyclotrimers under mild conditions and in few steps. The Negishi cross-coupling reaction was used for the C-C bond formation, whereas intramolecular O-alkylations provided the oxepane rings.