Ruthenium-catalysed one-pot regio- and diastereoselective synthesis of pyrrolo[1,2-a]indoles via cascade C-H functionalization/annulationElectronic supplementary information (ESI) available: Experimental procedures and analytical data of the products. CCDC 1567079 (3a) and 1567080 (5a). For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7cc06276a
A cascade approach has been developed towards dual C-C bond formation via consecutive C-H functionalization/cyclization giving access to pyrrolo[1,2- a ]indoles in a highly regio- and diastereoselective manner using catalytic [Ru( p -cymene)Cl 2 ] 2 . The methodology was further expanded to attain p...
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creator | Singh, Sukhdev Butani, Himanshu H Vachhani, Dipak D Shah, Anamik Van der Eycken, Erik V |
description | A cascade approach has been developed towards dual C-C bond formation
via
consecutive C-H functionalization/cyclization giving access to pyrrolo[1,2-
a
]indoles in a highly regio- and diastereoselective manner using catalytic [Ru(
p
-cymene)Cl
2
]
2
. The methodology was further expanded to attain pentacyclic structures involving manifold C-C bond creation.
Catalytic, regioselective and diastereoselective synthesis of pyrrolo[1,2-
a
]indoles through a cascade C-H activation and cyclization process. |
doi_str_mv | 10.1039/c7cc06276a |
format | Article |
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via
consecutive C-H functionalization/cyclization giving access to pyrrolo[1,2-
a
]indoles in a highly regio- and diastereoselective manner using catalytic [Ru(
p
-cymene)Cl
2
]
2
. The methodology was further expanded to attain pentacyclic structures involving manifold C-C bond creation.
Catalytic, regioselective and diastereoselective synthesis of pyrrolo[1,2-
a
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via
consecutive C-H functionalization/cyclization giving access to pyrrolo[1,2-
a
]indoles in a highly regio- and diastereoselective manner using catalytic [Ru(
p
-cymene)Cl
2
]
2
. The methodology was further expanded to attain pentacyclic structures involving manifold C-C bond creation.
Catalytic, regioselective and diastereoselective synthesis of pyrrolo[1,2-
a
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via
consecutive C-H functionalization/cyclization giving access to pyrrolo[1,2-
a
]indoles in a highly regio- and diastereoselective manner using catalytic [Ru(
p
-cymene)Cl
2
]
2
. The methodology was further expanded to attain pentacyclic structures involving manifold C-C bond creation.
Catalytic, regioselective and diastereoselective synthesis of pyrrolo[1,2-
a
]indoles through a cascade C-H activation and cyclization process.</abstract><doi>10.1039/c7cc06276a</doi><tpages>4</tpages></addata></record> |
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title | Ruthenium-catalysed one-pot regio- and diastereoselective synthesis of pyrrolo[1,2-a]indoles via cascade C-H functionalization/annulationElectronic supplementary information (ESI) available: Experimental procedures and analytical data of the products. CCDC 1567079 (3a) and 1567080 (5a). For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7cc06276a |
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