A highly efficient asymmetric imino-ene reaction of cyclic ketimines with silyl enol ethers was developed. Various chiral benzosultam derivatives were obtained in excellent yields (up to 99%), enantioselectivities (up to 99% ee), and diastereoselectivities (up to >19:1 dr) by utilizing a Ni(BF)·6HO/,-dioxide complex as the catalyst. A possible transition state model was proposed to explain the stereoinduction. Furthermore, the synthetic utility of the protocol provided quick access to optically pure HIV-1 inhibitor.
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http://dx.doi.org/10.1021/acs.orglett.0c00004 | DOI Listing |
J Org Chem
January 2024
Institut für Chemie, Technische Universität Berlin, Strasse des 17. Juni 115, 10623 Berlin, Germany.
The syntheses of hexabrominated -carborates decorated with different chiral Binol-derived phosphonates and their conjugate acids are described. X-ray diffraction analysis reveals a polymeric structure for the sodium salt with the anionic units connected by [B-Br-Na-O═P] linkages. For the acid, coordination of the proton to the phosphonate's P═O oxygen atom is assumed.
View Article and Find Full Text PDFChem Commun (Camb)
February 2022
Department of Chemistry, School of Science, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.
Catalytic imino-ene-type allylation reactions of unactivated allyl compounds were achieved. In the presence of a catalytic amount of a strongly basic KOBu-LiTMP or NaOBu-LiTMP mixed system, the desired reactions proceeded smoothly at low temperature. Notably, a gaseous alkene, propylene, could also be used in this reaction system.
View Article and Find Full Text PDFOrg Lett
February 2020
Key Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry , Sichuan University, Chengdu 610064 , China.
A highly efficient asymmetric imino-ene reaction of cyclic ketimines with silyl enol ethers was developed. Various chiral benzosultam derivatives were obtained in excellent yields (up to 99%), enantioselectivities (up to 99% ee), and diastereoselectivities (up to >19:1 dr) by utilizing a Ni(BF)·6HO/,-dioxide complex as the catalyst. A possible transition state model was proposed to explain the stereoinduction.
View Article and Find Full Text PDFJ Org Chem
April 2019
Jiangsu Key Laboratory of Advanced Catalytic Materials & Technology, School of Pharmaceutical Engineering & Life Science , Changzhou University, Changzhou 213164 , P. R. China.
Intramolecular imino-ene reaction of 2 H-aziridine has been studied experimentally and computationally, demonstrating that (1) the concerted process takes place regioselectively on the alkene E-CH group; (2) the geometry of the N-linker impacts the reaction activation energy and diastereoselectivity significantly, with pyramidal alkyl amine as the linkage, an exclusive cis-product is achieved; (3) when the reaction has to occur with the Z-CH group, the cis-diastereoselectivity is solely observed regardless of the nature of the N-linkage.
View Article and Find Full Text PDFOrg Lett
June 2018
Jiangsu Key Laboratory of Advanced Catalytic Materials & Technology, School of Pharmaceutical Engineering & Life Science , Changzhou University, Changzhou 213164 , People's Republic of China.
A range of novel (poly)cyclic alkaloids incorporating an unprecedented 1,5-diazaspiro[2.4]heptane core that carry a spiro NH aziridine moiety and a 7-vinyl group are constructed from the thermal reaction of vinyl azides with tethered alkenes. Vinyl azides are converted to 2H-azirines in situ, which serve as enophiles for intramolecular imino-ene reactions with suitable alkenes.
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