Over 160 chiral vicinal bromochlorinated natural products have been identified; however, a lack of synthetic methods for the selective incorporation of halogens into organic molecules has hindered their synthesis. Here we disclose the first total synthesis and structural confirmation of isoplocamenone and plocamenone, as well as the first selective and scalable synthesis of the preclinical anticancer natural product halomon. The synthesis of these inter-halogenated compounds has been enabled by our recently developed chemo-, regio-, and enantioselective dihalogenation reaction
International audienceA short enantioselective catalytic synthesis of the key C15−C27 fragment of ba...
International audienceA short enantioselective catalytic synthesis of the key C15−C27 fragment of ba...
Herein we describe a highly chemo-, regio-, and enantioselective bromochlorination reaction of allyl...
Over 160 chiral vicinal bromochlorinated natural products have been identified; however, a lack of ...
Over 160 chiral vicinal bromochlorinated natural products have been identified; however, a lack of ...
Here we describe the realization of a one-pot protocol for the β-C–H halogenation of cyclic enones v...
Here we describe the realization of a one-pot protocol for the β-C–H halogenation of cyclic enones v...
Herein, a regioselective bromination or chlorination reaction of 1‐naphthaldehydes is described. Wit...
Herein, a regioselective bromination or chlorination reaction of 1‐naphthaldehydes is described. Wit...
Herein, a regioselective bromination or chlorination reaction of 1‐naphthaldehydes is described. Wit...
Herein, a regioselective bromination or chlorination reaction of 1‐naphthaldehydes is described. Wit...
A short enantioselective catalytic synthesis of the key C15–C27 fragment of bastimolide A, a natural...
Herein we describe a highly chemo-, regio-, and enantioselective bromochlorination reaction of allyl...
Herein we describe a highly chemo-, regio-, and enantioselective bromochlorination reaction of allyl...
International audienceA short enantioselective catalytic synthesis of the key C15−C27 fragment of ba...
International audienceA short enantioselective catalytic synthesis of the key C15−C27 fragment of ba...
International audienceA short enantioselective catalytic synthesis of the key C15−C27 fragment of ba...
Herein we describe a highly chemo-, regio-, and enantioselective bromochlorination reaction of allyl...
Over 160 chiral vicinal bromochlorinated natural products have been identified; however, a lack of ...
Over 160 chiral vicinal bromochlorinated natural products have been identified; however, a lack of ...
Here we describe the realization of a one-pot protocol for the β-C–H halogenation of cyclic enones v...
Here we describe the realization of a one-pot protocol for the β-C–H halogenation of cyclic enones v...
Herein, a regioselective bromination or chlorination reaction of 1‐naphthaldehydes is described. Wit...
Herein, a regioselective bromination or chlorination reaction of 1‐naphthaldehydes is described. Wit...
Herein, a regioselective bromination or chlorination reaction of 1‐naphthaldehydes is described. Wit...
Herein, a regioselective bromination or chlorination reaction of 1‐naphthaldehydes is described. Wit...
A short enantioselective catalytic synthesis of the key C15–C27 fragment of bastimolide A, a natural...
Herein we describe a highly chemo-, regio-, and enantioselective bromochlorination reaction of allyl...
Herein we describe a highly chemo-, regio-, and enantioselective bromochlorination reaction of allyl...
International audienceA short enantioselective catalytic synthesis of the key C15−C27 fragment of ba...
International audienceA short enantioselective catalytic synthesis of the key C15−C27 fragment of ba...
International audienceA short enantioselective catalytic synthesis of the key C15−C27 fragment of ba...
Herein we describe a highly chemo-, regio-, and enantioselective bromochlorination reaction of allyl...