Asymmetric reduction of 4-trimethylsilyl-3-butyn-2-one to (R)-4-trimethylsilyl-3-butyn-2-ol catalyzed by a novel strain lyophilized Acetobacter sp. CCTCC M209061 in an aqueous/ionic liquid biphasic system
Author:
Funder
Shaoguan Science and Techonolgy Department
Publisher
Springer Science and Business Media LLC
Subject
Physical and Theoretical Chemistry,Catalysis
Link
https://link.springer.com/content/pdf/10.1007/s11144-022-02223-9.pdf
Reference32 articles.
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2. Zhu WR, Su Q, Diao HJ et al (2020) Enantioselective dehydrative γ-arylation of α-indolyl propargylic alcohols with phenols: Access to chiral tetrasubstituted allenes and naphthopyrans. Org Lett 22:6873–6878. https://doi.org/10.1021/acs.orglett.0c02386
3. Nandi GC, Rathman BM, Laali KK (2013) Mild conversion of propargylic alcohols to α, β-unsaturated enones in ionic liquids (ILs); a new ‘metal free’ life for the Rupe rearrangement. Tetrahedron Lett 46:6258–6263. https://doi.org/10.1016/j.tetlet.2013.09.028
4. Silva ABV, Silva ED, dos Santos AA et al (2020) A sustainable access to ynones through laccase/TEMPO-catalyzed metal- and halogen-free aerobic oxidation of propargylic alcohols in aqueous medium. Catal Commun. https://doi.org/10.1016/j.catcom.2020.105946
5. Li ML, Abdolmohammadi S, Hoseininezhad-Namin MS et al (2020) Carboxylative cyclization of propargylic alcohols with carbon dioxide: A facile and Green route to α-methylene cyclic carbonates. J CO2 Util 38:220–231. https://doi.org/10.1016/j.jcou.2020.01.024
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