A full account of the concise total syntheses of dictyodendrins B and E, and the formal synthesis of dictyodendrin C are described. A palladium-catalysed Larock indole synthesis was used to form the highly substituted indole core, and a palladium-mediated one-pot consecutive Buchwald-Hartwig amination/C-H activation reaction was used to construct the key pyrrolo[2,3-c]carbazole core. Unsuccessful synthetic strategies are also discussed.http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000341769700015&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=8e1609b174ce4e31116a60747a720701Chemistry, OrganicSCI(E)6ARTICLEyxjia@bjmu.edu.cn265735-574
Department of ChemistryC-C and C-N bond formation in organic synthesis is a very important process. ...
Dictyoxetane, a structurally novel diterpene, is related to the dollabellane class of natural produc...
The 2,4-dihydropyrrolo[3,4-b] indole ( 5) was prepared by the intramolecular 1,3-dipolar cycloaddit...
Syntheses of dictyodendrins A and F have been achieved using a sequential C–H functionalization stra...
The concise synthesis of the novel telomerase inhibitors dictyodendrins B and E was completed in onl...
A concise total synthesis of dictyodendrin B (1) is reported, a scarce marine alkaloid endowed with ...
A formal synthesis of the telomerase inhibitory marine pyrrolocarbazole alkaloid dictyodendrin B is ...
Concise and flexible total syntheses of the pyrrolo[2,3-c]carbazole alkaloids dictyodendrin B (2), C...
The dictyodendrin alkaloids have been described as the first telomerase inhibitors of marine origin....
The synthesis of biologically active core structures such as indoles, imidazoles and pyrrolo-[2,1-j]...
A new indole synthesis is described. The key step involves a novel tin-mediated free radical reactio...
A straightforward assembly of polysubstituted 1,2-dihydro-3H-pyrrolo[1,2-a]indol-3-ones through a do...
A straightforward assembly of polysubstituted 1,2-dihydro-3H-pyrrolo[1,2-a]indol-3-ones through a do...
Thesis (S.M.)--Massachusetts Institute of Technology, Dept. of Chemistry, 2005.Includes bibliographi...
AbstractA Unified Approach Toward the Total Syntheses ofPrenylated Indole Alkaloid Natural Productsb...
Department of ChemistryC-C and C-N bond formation in organic synthesis is a very important process. ...
Dictyoxetane, a structurally novel diterpene, is related to the dollabellane class of natural produc...
The 2,4-dihydropyrrolo[3,4-b] indole ( 5) was prepared by the intramolecular 1,3-dipolar cycloaddit...
Syntheses of dictyodendrins A and F have been achieved using a sequential C–H functionalization stra...
The concise synthesis of the novel telomerase inhibitors dictyodendrins B and E was completed in onl...
A concise total synthesis of dictyodendrin B (1) is reported, a scarce marine alkaloid endowed with ...
A formal synthesis of the telomerase inhibitory marine pyrrolocarbazole alkaloid dictyodendrin B is ...
Concise and flexible total syntheses of the pyrrolo[2,3-c]carbazole alkaloids dictyodendrin B (2), C...
The dictyodendrin alkaloids have been described as the first telomerase inhibitors of marine origin....
The synthesis of biologically active core structures such as indoles, imidazoles and pyrrolo-[2,1-j]...
A new indole synthesis is described. The key step involves a novel tin-mediated free radical reactio...
A straightforward assembly of polysubstituted 1,2-dihydro-3H-pyrrolo[1,2-a]indol-3-ones through a do...
A straightforward assembly of polysubstituted 1,2-dihydro-3H-pyrrolo[1,2-a]indol-3-ones through a do...
Thesis (S.M.)--Massachusetts Institute of Technology, Dept. of Chemistry, 2005.Includes bibliographi...
AbstractA Unified Approach Toward the Total Syntheses ofPrenylated Indole Alkaloid Natural Productsb...
Department of ChemistryC-C and C-N bond formation in organic synthesis is a very important process. ...
Dictyoxetane, a structurally novel diterpene, is related to the dollabellane class of natural produc...
The 2,4-dihydropyrrolo[3,4-b] indole ( 5) was prepared by the intramolecular 1,3-dipolar cycloaddit...