Unknown

Dataset Information

0

Synthesis of Chromenoimidazoles, Annulated with an Azaindole Moiety, through a Base-Promoted Domino Reaction of Cyano­methyl Quaternary Salts.


ABSTRACT: The reactivity of -cyanomethyl quaternary salts of 4-, 5- and 7-azaindoles towards salicylic aldehydes has been studied. The interaction of azaindolium salts with salicylic aldehydes proceeds as a base-promoted domino reaction, giving the corresponding chromenoimidazopyrrolopyridines. In the case of the 7-(cyanomethyl)-7-azaindolium salt, the reaction was found to be more sensitive, but the use of the 1-methyl-substituted salt allowed the synthesis of the desired compounds, incorporating the heterocyclic core of isogranulatimide C, a marine natural product.

SUBMITTER: Voskressensky LG 

PROVIDER: S-EPMC6193216 | biostudies-other | 2017 Jun

REPOSITORIES: biostudies-other

Similar Datasets

| S-EPMC6220673 | biostudies-literature
| S-EPMC6641896 | biostudies-literature
| S-EPMC6466694 | biostudies-literature
| S-EPMC5474666 | biostudies-literature
| S-EPMC4648040 | biostudies-literature
| S-EPMC6647956 | biostudies-literature
| S-EPMC7663467 | biostudies-literature
| S-EPMC8524416 | biostudies-literature
| S-EPMC3596043 | biostudies-other
| S-EPMC6280151 | biostudies-literature