marinoquinoline-a has been researched along with 6-azaindole* in 1 studies
1 other study(ies) available for marinoquinoline-a and 6-azaindole
Article | Year |
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Formation of 6-Azaindoles by Intramolecular Diels-Alder Reaction of Oxazoles and Total Synthesis of Marinoquinoline A.
A new variant of the intramolecular Diels-Alder oxazole (IMDAO) cycloaddition that provides direct access to 6-azaindoles was developed. The IMDAO reaction was applied in a total synthesis of the aminophenylpyrrole-derived alkaloid marinoquinoline A, also featuring the use of a Curtius reaction for preparation of a 5-aminooxazole, a propargylic C,H-bond insertion, an Topics: Alkynes; Aza Compounds; Cycloaddition Reaction; Indoles; Oxazoles; Pyrroles; Quinolines | 2020 |