Zobrazeno 1 - 10
of 79
pro vyhledávání: '"Jinbao Xiang"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 17, Iss 1, Pp 2505-2510 (2021)
A base- and catalyst-free C(sp3)–H allylic alkylation of 2-alkylpyridines with Morita–Baylis–Hillman (MBH) carbonates is described. A plausible mechanism of the reaction might involve a tandem SN2’ type nucleophilic substitution followed by a
Externí odkaz:
https://doaj.org/article/9cd53c09b13a49bc831ac09e4af14b33
Publikováno v:
The Journal of Organic Chemistry. 88:3636-3649
Autor:
Shulin Ning, Lianyou Zheng, Qiansong Gao, Lingling Shi, Yueling Liu, Chengcheng Sun, Zhuoqi Zhang, Jinbao Xiang
Publikováno v:
Green Chemistry. 24:5632-5636
A practical electrochemical method for the selective deprotection of the pMCB group was reported, which provides an efficient protocol for the controlled release of carboxylic acids, phosphoric acids and alcohols.
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 17, Iss 1, Pp 2505-2510 (2021)
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry
A base- and catalyst-free C(sp3)–H allylic alkylation of 2-alkylpyridines with Morita–Baylis–Hillman (MBH) carbonates is described. A plausible mechanism of the reaction might involve a tandem SN2’ type nucleophilic substitution followed by a
Autor:
Lingling Shi, Lianyou Zheng, Shulin Ning, Qiansong Gao, Chengcheng Sun, Zhuoqi Zhang, Jinbao Xiang
Publikováno v:
Organic letters. 24(31)
An efficient electrooxidative dearomatization of inactive biphenyls has been developed under mild and easy-to-operate conditions. The protocol provides a powerful tool for the rapid synthesis of cyclohexadienones in moderate to high yields with wide
Autor:
Siyu Wang, Zhuoqi Zhang, Chunxi Wen, Qiansong Gao, Shaoli Song, Shutao Wang, Lianyou Zheng, Jinbao Xiang
Publikováno v:
The Journal of Organic Chemistry. 86:6458-6466
A one-pot synthetic method for indole/pyrrole-fused 1,4-diazepanone scaffolds has been developed. This method involves a sequential amide coupling/intramolecular aza-Michael addition of 1H-indole/pyrrole-2-carboxylic acids with Morita-Baylis-Hillman-
Publikováno v:
Organic Letters. 23:2298-2302
An efficient and practical electrochemical method for selective reduction of cyclic imides has been developed using a simple undivided cell with carbon electrodes at room temperature. The reaction provides a useful strategy for the rapid synthesis of
Publikováno v:
ACS Applied Energy Materials. 3:9449-9458
The morphology and electronic structure dual modulation is an effective strategy to optimize the performance of the electrocatalysts. Herein, a hydrangea-like vanadium-doped FeNi2P hybrid material ...
Publikováno v:
Chemistry, an Asian journal. 17(1)
A controllable and regiodivergent N-allylation reaction involving readily available O-alkyl hydroxamates derived from natural α-amino acids has been developed, allowing regiospecific access to α/β-dipeptides containing α-unsaturated β-amino acid
Autor:
Nian Liu, Bowen Gong, Wenxia Xie, Zhuoqi Zhang, Lianyou Zheng, Jinbao Xiang, Xin Che, Shulin Ning
Publikováno v:
Synlett. 30:2077-2080
A diethyl phosphite mediated electrochemical oxidation strategy for the synthesis of 3,4-dihydroisoquinolin-1(2H)-ones from tetrahydroisoquinolines under mild conditions has been developed. This protocol provides an environmentally friendly and simpl