相关期刊:《Chemical Research in Chinese Universities》《Chinese Journal of Structural Chemistry》《Green Synthesis and Catalysis》《Chinese Journal of Chemistry》更多>>
We thank the Qingdao Marine Science and Technology Center(No.2022QNLM030003-2);the Fundamental Research Funds for the Central Universities,Taishan Scholar Program of Shandong Province(No.tsqn201909056);National Natural Science Foundation of China(No.22171251)for financial support.
An efficient asymmetric[4+2]cyclization of hydroxyphenyl indolinone with azlactone for the synthesis of spirooxindoleδ-lactone has been developed,which realized the first asymmetric reaction of hydroxyphenyl indolino...
financial support of National Natural Science Foundation of China(21901193,22271314 and 22377097);the innovation foundation of Key Laboratory of Green Chemical Engineering Process of Ministry of Education(GCX2023002).
Concise assembly of spirooxindoles is of great significance but a challenging task in modern organic synthesis.Described herein is an unusual base-promoted[4+2]spiroannulation of rarely used isatin-derivedβ-silylcarb...
We are grateful to the National Natural Science Foundation of China(Nos.21572196,21871227);the Priority Academic Program Development of Jiangsu Higher Education Institutions(No.BK2013016)for financial support.
A new DBU-catalyzed formal[4+2]cycloaddition between ortho-hydroxyphenyl-substituted para-quinone methides and electron-deficient dienophiles including 3-methyleneoxindoles and 2-aryldeneindene-1,3-diones was establis...
We are grateful for the financial support from the National Natural Science Foundation of China(81773889,22001024,82073998);the Sichuan Science and Technology Program(22CXRC0077,2021YFS0044);the Xinglin Scholar Research Premotion Project of Chengdu University of TCM.
Organocatalytic asymmetric[3+3]annulations of isatin-derived MBH carbonates and indolin-2-imines were efficiently achieved.This appears to be the first enantioselective approach for using isatin-derived MBH carbonates...
support from the National Natural Science Foundation of China(nos.21702184,21772175,and 91956117).
Highly enantioselective and diastereoselective 1,2-diarylation and 1,2-arylalkynylation of trisubstituted alkenes are reported via the palladium-catalyzed Heck/Suzuki or Heck/Sonogashira domino sequence.These alkenes ...
financial support from Ministry of Science and Technology of China (No.2019ZX09721001-008);National Natural Science Foundation of China (Nos.81773890,22001024,82073997);the “Thousand Talents Program” of Sichuan Province and Xinglin Scholar Research Premotion Project of CDUTCM。
An N-heterocyclic carbene(NHC)-catalysed retro-aldol/aldol cascade reaction of spirooxindole-basedβ-hydroxyaldehyde has been developed.The ring opening-closure process enables the diastereodivergent synthesis of spir...
supported by grants from the National Natural Science Foundation(Nos.21772131,81672552,81773890,82073997);the Fundamental Research Funds of Science&Technology Department of Sichuan Province(Nos.2019YFSY0004,2017JY0226,2019YFS0298);Project First-Class Disciplines Development supported by CDUTCM。
A series of spirooxindole-ferrocene hybrids bearing five or four contiguous chiral centers were designed and synthesized via organocatalysis.In vitro protein binding and cellular proliferation assays suggested that co...
Financial support from SZSTI(Nos.JCY120170817110515599,KQTD20150717103157174);the National Natural Science Founda tion of China(Nos.21772082 and 21971104);the Guangdong Innovative Program(No.2019BT02Y335);the Guangdong Provin cial Key Laboratory of Catalysis(No.2020B121201002);the Shen zhen Key Laboratory of Small Molecule Drug Discovery and Syn thesis(No.ZDSY520190902093215877);the Shenzhen Nobel Prize Scientists Laboratory Project(C17783101)is greatly appreci-ated.The authors are grateful to Prof.Qing Ye(SUSTech)for assis-tance with XRD analysis.
Owing to their challenging structures and promising biological profiles,spirooxindole alkaloids have long attracted much attention from the synthetic community.Herein,we wish to describe a concise,protecting-group-fre...
financial support from the National Natural Science Foundation of China(81573588,81630101,81773889 and 21772131);the Science&Technology Department of Sichuan Province(2017JZYD0001,2017JQ0002,2017JY0323 and 2019YFSY0004,China)
Simultaneous inhibition of MDM2 and CDK4 may be an effective treatment against glioblastoma. A collection of chiral spirocyclic tetrahydronaphthalene(THN)-oxindole hybrids for this purpose have been developed. Appropr...
the National Natural Science Foundation of China(No.51373067).
A straiglitforward and efficient synthetic method of 2′-(dialkylammo)-l-alkyl-4′H-spiro[indoline-3,5′-oxazole]-2,4′-diones and 2-(dialkylamino)-5,6-dihydro-4H-naphtho[2,1-e][1,3]oxazin-4-one-derivatives have been ...