the Independent Research Foundation of Key Laboratory of Green and Precise Synthetic Chemistry and Applications in Huaibei Normal University,Ministry of Education;the University Top Talents Academic Funding Project of Anhui Province(gxbjzD2021097);the Natural Science Foundation of Educational Committee from Anhui Province and Huaibei Normal University(KJ2020A0045,KJ2020A1199,KJ2020B01,2023ZK078,2023ZK079);the University Synergy Innovation Program of Anhui Province(GXXT-2020-078)for financial support of this work.
Herein,a DMAP-catalyzed[4+2]annulation ofα-substituted allenoates with arylazosulfones is reported,which affords facile access to tetrahydropyridazine derivative in synthetically useful yields.This reaction features ...
Financial support from the Fundamental Research Funds for the Central Universities (No. KYZ201749) and the National Natural Science Foundation of China (Nos. 21272119, J1103306) are gratefully acknowledged.
A phosphine-catalyzed [4+2] annulation of a-substituted allenoate with exocyclic alkene moiety of oxindoles or indan-1,3-diones has been developed. Thus, under the catalysis of PPh3 (20 mol%), a series of spirooxin...
In contrast with the reported phosphine- and DABCO-catalyzed [3 + 2] and [2 +2] annulation of allenoates with trifluoromethylketone, the [2+2+2] annulation of allenoates and two molecules of trifluoromethylketone ...
2,3-Allenols were prepared conveniently from the reduction reaction of 2, 3-allenoates with DIBAL-H (Diisobutylaluminum hydride) in toluene. A dramatic solvent effect was observed for this reaction.
National Natural Science Foundation of China (No. 29525202);Shanghai Municipal Cormnittee of Science and Technology (No. 98QA14001).
The hydrohalogenation reaction of 1-alkyl substituted 1,2-allenyl carboxylic acid esters (1) with MX (M= Na, or Li, X= Cl, Br, I) afforded a mixture of β,γ-unsaturated 3-halo–3-alkenoates (2) and Q,P unsaturated 3-...