Gold(I)-Catalyzed\n6-<i>exo</i>-<i>dig</i> Hydroamination/7-<i>endo</i>-<i>dig</i> Cycloisomerization\nDomino Approach to 3,7<i>a</i>‑Diazacyclohepta[<i>jk</i>]fluorene Derivativ

A series\nof 3,7<i>a</i>-diazacyclohepta[<i>jk</i>]fluorene\nderivatives were synthesized via a gold(I)-catalyzed 6-<i>exo</i>-<i>dig</i> hydroamination/7-<i>endo</i>-<i>dig</i> cycloisomerization domino method. The method\nexhibits a broad substrate scope, and a plausible mechanism has been\nproposed. The efficacy of this\nstrategy is further validated by the successful derivatization of\n3,7<i>a</i>-diazacyclohepta[<i>jk</i>]fluorene.

Publication Details

Journal
Figshare
Published
2024-11-14
DOI
https://doi.org/10.1021/acs.orglett.4c03926.s001
Primary Topic
Catalytic Alkyne Reactions
Type
article
Field-Weighted Citation Impact
0.00
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article

Gold(I)-Catalyzed\n6-exo-dig Hydroamination/7-endo-dig Cycloisomerization\nDomino Approach to 3,7a‑Diazacyclohepta[jk]fluorene Derivativ

Figshare
Catalytic Alkyne Reactions
article

Gold(I)-Catalyzed\n6-exo-dig Hydroamination/7-endo-dig Cycloisomerization\nDomino Approach to 3,7a‑Diazacyclohepta[jk]fluorene Derivativ

article en

Abstract

A series\nof 3,7<i>a</i>-diazacyclohepta[<i>jk</i>]fluorene\nderivatives were synthesized via a gold(I)-catalyzed 6-<i>exo</i>-<i>dig</i> hydroamination/7-<i>endo</i>-<i>dig</i> cycloisomerization domino method. The method\nexhibits a broad substrate scope, and a plausible mechanism has been\nproposed. The efficacy of this\nstrategy is further validated by the successful derivatization of\n3,7<i>a</i>-diazacyclohepta[<i>jk</i>]fluorene.

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Openalex Percentile: Top 79%
Catalytic Alkyne Reactions
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Gold(I)-Catalyzed\n6-<i>exo</i>-<i>dig</i> Hydroamination/7-<i>endo</i>-<i>dig</i> Cycloisomerization\nDomino Approach to 3,7<i>a</i>‑Diazacyclohepta[<i>jk</i>]fluorene Derivativ · Figshare (2024) | TGRS Research Map | TGRS