Spiroannulations\nof\nβ‑Ketothioamides\nwith Bromoenals via Selective <i>C</i>‑Michael Addition\nand <i>S</i>‑Michael Addition-Triggered Cascade Reactions

A spiroannulation\nreaction of β-ketothioamides with aromatic\nβ-bromoenals and aromatic α-bromoenals via selective <i>C</i>-Michael addition and <i>S</i>-Michael addition-triggered\ncascade reactions has been developed. This protocol provides a novel\nand rapid approach for the synthesis of substituted spirothiopyran\nand spirothiophene derivatives under mild conditions with moderate\nto good yields and a broad substrate scope.

Publication Details

Journal
Figshare
Published
2024-09-30
DOI
https://doi.org/10.1021/acs.joc.4c01668.s001
Primary Topic
Synthesis of heterocyclic compounds
Type
article
Field-Weighted Citation Impact
0.00
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article

Spiroannulations\nof\nβ‑Ketothioamides\nwith Bromoenals via Selective C‑Michael Addition\nand S‑Michael Addition-Triggered Cascade Reactions

Figshare
Synthesis of heterocyclic compounds
article

Spiroannulations\nof\nβ‑Ketothioamides\nwith Bromoenals via Selective C‑Michael Addition\nand S‑Michael Addition-Triggered Cascade Reactions

article en

Abstract

A spiroannulation\nreaction of β-ketothioamides with aromatic\nβ-bromoenals and aromatic α-bromoenals via selective <i>C</i>-Michael addition and <i>S</i>-Michael addition-triggered\ncascade reactions has been developed. This protocol provides a novel\nand rapid approach for the synthesis of substituted spirothiopyran\nand spirothiophene derivatives under mild conditions with moderate\nto good yields and a broad substrate scope.

Figshare
Openalex Percentile: Top 76%
Synthesis of heterocyclic compounds
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Spiroannulations\nof\nβ‑Ketothioamides\nwith Bromoenals via Selective <i>C</i>‑Michael Addition\nand <i>S</i>‑Michael Addition-Triggered Cascade Reactions · Figshare (2024) | TGRS Research Map | TGRS