Stereoselective functionalization at C-2 and C-3 of the gibberellin skeleton was achieved via an intramolecular free radical cyclization approach using a tethered C-19 halomethyl ester as the radical precursor.
Pseudolaric acids are a family of diterpenoid natural products that exhibit a broad spectrum of biological activities.The main structural feature of their framework is a trans-fused perhydroazulene bearing a bridged l...Pseudolaric acids are a family of diterpenoid natural products that exhibit a broad spectrum of biological activities.The main structural feature of their framework is a trans-fused perhydroazulene bearing a bridged lactone positioned at the junction of the rings.Herein,we have developed a radical cyclization strategy that allows flexible tuning of the cyclization process through diverse silicon substitutions on the substrates.This strategy can assist in constructing a series of skeletons with structural resemblance to pseudolaric acids and expedites the construction of the bridged lactone.Finally,it facilitates the synthesis of the entire skeletal structure of the pseudolaric acidfamily of natural products,excludingthe B-ringfunctionalization.展开更多
3-CF3 S substituted thioflavones and benzothiophenes were achieved via the reactions of AgSCF3 with methylthiolated alkynones and alkynylthioanisoles,respectively,promoted by persulfate.This protocol possesses good fu...3-CF3 S substituted thioflavones and benzothiophenes were achieved via the reactions of AgSCF3 with methylthiolated alkynones and alkynylthioanisoles,respectively,promoted by persulfate.This protocol possesses good functional group tolerance and high yields.Mechanistic studies suggested that a classic two-step radical process was involved,which includes addition of CF3 S radical to triple bond and cyclization with SMe moiety.展开更多
Visible-light photoredox catalysis is a powerful and attractive strategy for organic molecule activation and new reaction design owing to its environmental-friendly characteristics and unique catalytic mechanisms,and ...Visible-light photoredox catalysis is a powerful and attractive strategy for organic molecule activation and new reaction design owing to its environmental-friendly characteristics and unique catalytic mechanisms,and has found wide applications in organic synthesis.This catalytic strategy enables controllable generation of diverse nitrogen-centered radicals(NCRs)under mild conditions,providing access to construction of diverse nitrogencontaining compounds.In this review,we critically illustrate the recent advances in the field of visible-light photoredox-catalyzed cyclization of nitrogen-centered radicals,based on the different radical precursors and activation modes.Wherever possible,particular emphasis is also put on working models and synthetic applications.展开更多
An efficient method for the synthesis of functionalized chroman-4-ones induced by visible light via the radical cyclization reaction of sulfinic acids and o-(allyloxy)arylaldehydes at room temperature was described.Th...An efficient method for the synthesis of functionalized chroman-4-ones induced by visible light via the radical cyclization reaction of sulfinic acids and o-(allyloxy)arylaldehydes at room temperature was described.The corresponding products were isolated with moderate to good yields.Radical mechanism was proposed fo r this trans formation.Anti-microbial activity of some desired compounds we re screened.展开更多
A series of novel cyclic derivatives have been synthesized by utilizing a nickel powder mediated radical cyclization as the key step. The structures of the new compounds were confirmed by 1H-NMR and MS.
A new synthesis of the bridged [6-6-6] ABE tricyclic ring analogues of methyllycaconitine with the C-1 oxygenated substituents has been developed using an efficient aza-annulation of β-enamino ketone followed by a fa...A new synthesis of the bridged [6-6-6] ABE tricyclic ring analogues of methyllycaconitine with the C-1 oxygenated substituents has been developed using an efficient aza-annulation of β-enamino ketone followed by a facile decarboxylation to form BE rings.Subsequent elaboration to form the A ring was achieved by a transannular acyl radical cyclization with concomitant equipment of the key C-1 oxygen functionality.展开更多
文摘Stereoselective functionalization at C-2 and C-3 of the gibberellin skeleton was achieved via an intramolecular free radical cyclization approach using a tethered C-19 halomethyl ester as the radical precursor.
基金the National Natural Science Foundation of China(Nos.22071205,22301251 and 21772164)China Postdoctoral Science Foundation(2023M732942),NFFTBS(J1310024)+1 种基金NCETFJ,and PCSIRT is acknowledgedthe financial support(No.202005)from State Key Laboratory of Elemento-Organic Chemistry,Nankai University.
文摘Pseudolaric acids are a family of diterpenoid natural products that exhibit a broad spectrum of biological activities.The main structural feature of their framework is a trans-fused perhydroazulene bearing a bridged lactone positioned at the junction of the rings.Herein,we have developed a radical cyclization strategy that allows flexible tuning of the cyclization process through diverse silicon substitutions on the substrates.This strategy can assist in constructing a series of skeletons with structural resemblance to pseudolaric acids and expedites the construction of the bridged lactone.Finally,it facilitates the synthesis of the entire skeletal structure of the pseudolaric acidfamily of natural products,excludingthe B-ringfunctionalization.
基金the National Natural Science Foundation of China(Nos.21991123,21677094)for financial support。
文摘3-CF3 S substituted thioflavones and benzothiophenes were achieved via the reactions of AgSCF3 with methylthiolated alkynones and alkynylthioanisoles,respectively,promoted by persulfate.This protocol possesses good functional group tolerance and high yields.Mechanistic studies suggested that a classic two-step radical process was involved,which includes addition of CF3 S radical to triple bond and cyclization with SMe moiety.
基金The authors’works in this area have been sponsored by the National Natural Science Foundation of China(Nos.91856119,21971081,21622201,21820102003,91956201 and 21772053)the Program of Introducing Talents of Discipline to Universities of China(111 Program,No.B17019).
文摘Visible-light photoredox catalysis is a powerful and attractive strategy for organic molecule activation and new reaction design owing to its environmental-friendly characteristics and unique catalytic mechanisms,and has found wide applications in organic synthesis.This catalytic strategy enables controllable generation of diverse nitrogen-centered radicals(NCRs)under mild conditions,providing access to construction of diverse nitrogencontaining compounds.In this review,we critically illustrate the recent advances in the field of visible-light photoredox-catalyzed cyclization of nitrogen-centered radicals,based on the different radical precursors and activation modes.Wherever possible,particular emphasis is also put on working models and synthetic applications.
基金the National Natural Science Foundation of China(No.21772107)Shandong Province Key Research and Development Plan(No.2019GSF108017)。
文摘An efficient method for the synthesis of functionalized chroman-4-ones induced by visible light via the radical cyclization reaction of sulfinic acids and o-(allyloxy)arylaldehydes at room temperature was described.The corresponding products were isolated with moderate to good yields.Radical mechanism was proposed fo r this trans formation.Anti-microbial activity of some desired compounds we re screened.
基金This program was supported by National Key Basic Research Program(973)(No.G1998051125).
文摘A series of novel cyclic derivatives have been synthesized by utilizing a nickel powder mediated radical cyclization as the key step. The structures of the new compounds were confirmed by 1H-NMR and MS.
基金National Natural Science Foundation of China (Nos.21472129 and 21871190) for financial support of this work by grants。
文摘A new synthesis of the bridged [6-6-6] ABE tricyclic ring analogues of methyllycaconitine with the C-1 oxygenated substituents has been developed using an efficient aza-annulation of β-enamino ketone followed by a facile decarboxylation to form BE rings.Subsequent elaboration to form the A ring was achieved by a transannular acyl radical cyclization with concomitant equipment of the key C-1 oxygen functionality.
