Chem. Sci., 2024, Accepted ManuscriptDOI: 10.1039/D4SC04632C, Edge Article Open Access   This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence.Yu-Juan Ma, Fei Xu, Xin-Ye Ren, Fan-Yao Chen, Jie Pan, Jinhua …
Green Chem., 2024, Accepted ManuscriptDOI: 10.1039/D4GC03753G, PaperWei-Jung Chiu, Chung-Ming SunA Rh(III)-catalyzed additive-controlled regioselective [4+1] and [4+2] cyclization of benzoic acids with alkynyl esters/amides under the electrochemical c…
Chinese Journal of Chemistry, EarlyView.
Chinese Journal of Chemistry, EarlyView.
Chinese Journal of Chemistry, EarlyView.
Org. Biomol. Chem., 2024, Accepted ManuscriptDOI: 10.1039/D4OB01363H, CommunicationZhongwen Wang, Tianhang Song, Yifan Wu, Jun RenA concise synthesis of (–)-quinocarcinol methyl ester was accomplished with an overall yield of 39% through a 9-step longe…
Org. Biomol. Chem., 2024, Advance ArticleDOI: 10.1039/D4OB01343C, PaperAditi Boruah, Mohit L. Deb, Ranjit Thakuria, Pranjal K. BaruahL-Proline catalysed synthesis of poly-substituted pyridines and further α-C(sp3)–H oxygenation of the tertiary amine mo…
Org. Biomol. Chem., 2024, Accepted ManuscriptDOI: 10.1039/D4OB01373E, Paper Open Access   This article is licensed under a Creative Commons Attribution 3.0 Unported Licence.Etienne Bickel, Uli KazmaierNew bottromycin derivatives have been prepared …
A practical method for the debenzylation of aryl benzyl ethers has been developed using easy-to-operate I2 and Et3SiH, as well as the green solvent ethyl acetate. Halo, methoxy, ester, and nitro groups on the benzene ring of the aryl benzyl ether are compatible with this debenzylation. Control experiments revealed that Et3SiI, generated in situ, might be the actual promoter of the procedure. This method does not require a separate desilylation reaction to obtain phenol products.