Isolated from diverse cyanobacteria, the hapalindole family of indole alkaloids comprises
over 80 interrelated natural products. The family is further divided into several subclasses …

We report the total synthesis of (−)-N-methylwelwitindolinone C isonitrile, in addition to the
total syntheses of the 3-hydroxylated welwitindolinones. Our routes to these elusive natural …

We report the first total synthesis of (−)-N-methylwelwitindolinone C isothiocyanate. Our
route features a number of key transformations, including an indolyne cyclization to …

The photo-induced cleavage of C (sp2)–Cl bonds is an appealing synthetic tool in organic
synthesis, but usually requires the use of high UV light, photocatalysts and/or …

Described is a concise total synthesis of N-methylwelwitindolinone D isonitrile, the first in a
family of complex bicyclo [4.3. 1] decane-containing indole alkaloids to yield to synthesis …

An efficient and straightforward Lewis-acid-mediated stereoselective (4+ 3)-cyclization of
indole-substituted alkylidene malonates and donor–acceptor cyclopropanes has been …

Abstract The welwitindolinones with bicyclo [4.3. 1] cores are a class of natural products that
have attracted tremendous interest from the synthetic community because of their fascinating …

Total Synthesis of (−)-N-Methylwelwitindolinone B Isothiocyanate via a Chlorinative Oxabicycle
Ring-Opening Strategy | Journal of the American Chemical Society ACS ACS Publications …

As part of a comprehensive strategy to the welwitindolinone alkaloids possessing a bicyclo
[4.3. 1] decane core, we report herein concise asymmetric total syntheses of (−)-N …

The formal syntheses of N-methylwelwitindolinone C isothiocyanate, N-
methylwelwitindolinone C isonitrile, N-methylwelwitindolinone D isonitrile, 3-hydroxy-N …