DABCO-promoted reaction sequence of β-nitro alcohols and α-oxoaldehydes: construction of diverse tetrahydrofurans and total synthesis of (+)-bruguierol B

A DABCO-promoted highly efficient reaction sequence has been developed, where β-nitro alcohols reacted smoothly with α-oxoaldehydes to afford diverse tetrahydrofuran derivatives. This strategy enabled the first total synthesis of (+)-bruguierol B.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-10-09
DOI
https://doi.org/10.1039/d5qo01330e
Primary Topic
Asymmetric Synthesis and Catalysis
Type
article
Field-Weighted Citation Impact
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article

DABCO-promoted reaction sequence of β-nitro alcohols and α-oxoaldehydes: construction of diverse tetrahydrofurans and total synthesis of (+)-bruguierol B

Yankai Liu, Xuejiao Lv, Yu-Xia Lu
Organic Chemistry Frontiers
Asymmetric Synthesis and Catalysis
article

DABCO-promoted reaction sequence of β-nitro alcohols and α-oxoaldehydes: construction of diverse tetrahydrofurans and total synthesis of (+)-bruguierol B

Yankai Liu, Xuejiao Lv, Yu-Xia Lu
article en

Abstract

A DABCO-promoted highly efficient reaction sequence has been developed, where β-nitro alcohols reacted smoothly with α-oxoaldehydes to afford diverse tetrahydrofuran derivatives. This strategy enabled the first total synthesis of (+)-bruguierol B.

Organic Chemistry FrontiersVol. 13(1)
Qingdao National Laboratory for Marine Science and Technology (CN), Ocean University of China (CN)
Openalex Percentile: Top 79%
Asymmetric Synthesis and Catalysis
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