Organocatalytic Enantioselective Synthesis of Axially Chiral Tetrasubstituted Allenes via Direct 1,8-Addition to In Situ Formed Alkynyl 8-Methylenenaphthalen-2(8 H )-ones
Abstract
Organocatalytic enantioselective construction of axially chiral tetrasubstituted allenes has been achieved from the reaction between α-(2-hydroxynaphthalen-8-yl)propargylic alcohols and 2-arylindoles for the first time. With the aid of a suitable chiral phosphoric acid, alkynyl 8-methylenenaphthalen-2(8 H )-one was formed in situ from the corresponding α-(2-hydroxynaphthalen-8-yl)propargylic alcohol, followed by enantioselective 1,8-conjugate addition of 2-arylindole to afford the target axially chiral tetrasubstituted allenes in 70–95% yields with 64–94% ee. Notably, this work establishes the 2-hydroxynaphthalen-8-yl unit as an effective auxiliary group that enables the corresponding α-functionalized propargylic alcohols for the construction of enantioenriched tetrasubstituted allenes, which enrich the chemistry of quinone methides.
Fields of Study & Subjects
Axial and Atropisomeric Chirality Synthesis
Catalytic Alkyne Reactions
Synthesis of Indole Derivatives
Publication details
- Journal / source
- Organic Letters
- Publisher
- American Chemical Society (ACS)
- Volume
- 28
- Issue
- 4
- Pages
- 1374–1379
- Publication date
- 21 January 2026
- Language
- EN