about
Boron-substituted 1,3-dienes and heterodienes as key elements in multicomponent processes.Synthesis of 1-Amino-1H-Indenes via a Sequential Suzuki-Miyaura Coupling/Petasis Condensation Sequence.Synthesis of Polysubstituted Isoquinolines and Related Fused Pyridines from Alkenyl Boronic Esters via a Copper-Catalyzed Azidation/Aza-Wittig Condensation Sequence.Synthesis of Carbo[6]helicene Derivatives Grafted with Amino or Aminoester Substituents from Enantiopure [6]Helicenyl Boronates.Cross-metathesis/isomerization/allylboration sequence for a diastereoselective synthesis of anti-homoallylic alcohols from allylbenzene derivatives and aldehydes.Synthesis of alkenyl boronates from allyl-substituted aromatics using an olefin cross-metathesis protocol.Stereodivergent approach in the protected glycal synthesis of L-vancosamine, L-saccharosamine, L-daunosamine and L-ristosamine involving a ring-closing metathesis stepA DMAP-catalyzed mild and efficient synthesis of 1,2-dihydroquinazolines via a one-pot three-component protocolAccess to Fused Pyrroles from Cyclic 1,3-Dienyl Boronic Esters and Arylnitroso CompoundsFunction-Oriented Synthesis toward Peloruside A AnaloguesEne reactions of 2-borylated α-methylstyrenes: a practical route to 4-methylenechromanes and derivatives1,3-Dioxa-[3,3]-sigmatropic Oxo-Rearrangement of Substituted Allylic Carbamates: Scope and Mechanistic Studies
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Q38194136-6E11EE68-2613-4ECF-AF69-6E03699B76FDQ48091320-A3EA9923-23EA-47FA-AA98-9A6256328F6FQ48101100-F9C669F4-95FC-44D4-9071-A04B40B0C99AQ48147784-8B9A39C7-DC2E-4DA2-8346-1CEAEC397041Q51054703-6B0BD930-5987-4B77-BC36-637EDAB09BA4Q51804085-19163606-BD56-4D32-B1C8-AE89306A65D2Q59799740-A043D1FA-FA67-42F5-A368-355914373E29Q62870811-4B823788-DED7-4CD7-991C-23AE395AF00AQ90463326-4DFBF5D2-09B2-434F-A1E3-A1C84D8812EFQ92291767-414F5BE2-2E8F-4183-A574-C26C143634DCQ92334025-5D36E113-3261-4B88-85D4-857B246E7DC9Q93236024-A60BC10C-3DC9-454B-A91F-B9F0B51631F2
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description
researcher ORCID ID = 0000-0003-0529-715X
@en
wetenschapper
@nl
name
Bertrand Carboni
@ast
Bertrand Carboni
@en
Bertrand Carboni
@es
Bertrand Carboni
@nl
type
label
Bertrand Carboni
@ast
Bertrand Carboni
@en
Bertrand Carboni
@es
Bertrand Carboni
@nl
prefLabel
Bertrand Carboni
@ast
Bertrand Carboni
@en
Bertrand Carboni
@es
Bertrand Carboni
@nl
P31
P496
0000-0003-0529-715X