Regioselective Crossed Aldol Reactions under Mild Conditions via Synergistic Gold-Iron Catalysis
Document Type
Article
Publication Date
6-11-2020
Abstract
A synergistic gold-iron (Au-Fe) catalytic system was developed for sequential alkyne hydration and vinyl Au addition to aldehydes or ketones. Fe(acac)3 was identified as an essential co-catalyst in preventing vinyl Au protodeauration and facilitating nucleophilic additions. Effective C–C bond formation was achieved under mild conditions (room temperature) with excellent regioselectivity and high efficiency (1% [Au], up to 95% yields). The intramolecular reaction was also achieved, giving successful macrocyclization (16–31 ring sizes) with excellent yields (up to 90%, gram scale) without extended dilution (0.2 M), which highlights the great potential of this new crossed aldol strategy in challenging target molecule synthesis. Effective construction of the C–C bond is one of the most important tasks in organic synthesis. Whereas aldol condensation is a classic C–C bond-forming transformation, it requires other chemical promoters, such as strong base and reactive acidic catalysts. As a result, the overall transformation is limited in terms of ideal atom economy and environmentally friendly operation. With the discovery of a gold-iron (Au-Fe) synergistic catalysis system, here we describe a new approach to facilitating alkyne hydration and sequential vinyl Au addition to carbonyls. This approach gives the C–C bond-forming products in excellent yields, wide substrate scope, and great functional-group compatibility under mild conditions. This protocol can also be applied to macrocyclization without extended dilution. This C–C bond-forming strategy could facilitate challenging molecule synthesis in chemical, biological, and medicinal research. We report a synergistic gold-iron (Au-Fe) catalytic system to access vinyl Au reactivity by avoiding frequently occurring protodeauration. Fe(acac)3 was identified as an essential co-catalyst, facilitating vinyl Au addition to aldehydes. A broad substrate scope was obtained under mild conditions (room temperature) with excellent regioselectivity and high efficiency (1% [Au], up to 95% yields). This protocol offers a practical solution for achieving macrocyclization (16–31 ring sizes, up to 90%, gram scale) without extended dilution, highlighting the synthetic utility in complex molecular synthesis.
Identifier
85086096388 (Scopus)
Publication Title
Chem
External Full Text Location
https://doi.org/10.1016/j.chempr.2020.03.014
e-ISSN
24519294
ISSN
24519308
First Page
1420
Last Page
1431
Issue
6
Volume
6
Grant
1665122
Fund Ref
National Science Foundation
Recommended Citation
Yuan, Teng; Ye, Xiaohan; Zhao, Pengyi; Teng, Shun; Yi, Yaping; Wang, Jin; Shan, Chuan; Wojtas, Lukasz; Jean, Jonathan; Chen, Hao; and Shi, Xiaodong, "Regioselective Crossed Aldol Reactions under Mild Conditions via Synergistic Gold-Iron Catalysis" (2020). Faculty Publications. 5225.
https://digitalcommons.njit.edu/fac_pubs/5225
