Gold-Catalyzed Regio- and Diastereoselective [3 + 2] Cycloaddition/Unactivated C(sp<sup>3</sup>)–H Bond Insertion of <i>o</i>-1,6-Enynyl Benzaldehydes to <i>Oxa</i>-Bridged Polycycles

An efficient and expeditious method to assemble <i>oxa</i>-bridged polycycles bearing up to six contiguous stereocenters from a gold(I)-catalyzed [3 + 2] cycloaddition/unactivated C(sp<sup>3</sup>)-H bond insertion cascade of <i>o</i>-1,6-enynyl benzaldehydes at a low catalyst loading of 2 mol % is described.

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Publication Details

Journal
Organic Letters
Published
2025-04-04
DOI
https://doi.org/10.1021/acs.orglett.5c00891
Citations
1
Primary Topic
Catalytic Alkyne Reactions
Type
article
Field-Weighted Citation Impact
0.94

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article

Gold-Catalyzed Regio- and Diastereoselective [3 + 2] Cycloaddition/Unactivated C(sp3)–H Bond Insertion of o-1,6-Enynyl Benzaldehydes to Oxa-Bridged Polycycles

Rui Hu, Weidong Rao, Philip Wai Hong Chan, Xiaowen Ji et al.
1 citations
Organic Letters
Catalytic Alkyne Reactions
0.94
article

Gold-Catalyzed Regio- and Diastereoselective [3 + 2] Cycloaddition/Unactivated C(sp3)–H Bond Insertion of o-1,6-Enynyl Benzaldehydes to Oxa-Bridged Polycycles

Rui Hu, Weidong Rao, Philip Wai Hong Chan, Xiaowen Ji, Yongsheng Zhang
article en
1 citations

Abstract

An efficient and expeditious method to assemble <i>oxa</i>-bridged polycycles bearing up to six contiguous stereocenters from a gold(I)-catalyzed [3 + 2] cycloaddition/unactivated C(sp<sup>3</sup>)-H bond insertion cascade of <i>o</i>-1,6-enynyl benzaldehydes at a low catalyst loading of 2 mol % is described.

Organic LettersVol. 27(15)
Nanjing Forestry University (CN), Australian Regenerative Medicine Institute (AU), Monash University (AU)
Jiangsu Provincial Department of Education, Australian Research Council
Openalex Percentile: Top 27%
Catalytic Alkyne Reactions
0.94
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