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Synthesis of Cyclopropenes and Fluorinated Cyclopropanes via Michael Initiated Ring Closure of Alkyl Triflones

Chemistry : a European journal, 2022-04, Vol.28 (23), p.e202104364-n/a

2022

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Chemo-, regio- and stereoselective synthesis of monofluoroalkenes via a tandem fluorination–desulfonation sequence

Chemical communications (Cambridge, England), 2021-08, Vol.57 (63), p.7802-7805

2021

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Chameleonic Reactivity of Imidoyl Sulfoxonium Ylides: Access to Functionalized Pyrroles and Dihydro-pyridines

Organic letters, 2024-01, Vol.26 (1), p.62-67

2024

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Base promoted gem-difluoroolefination of alkyl triflones

Chemical communications (Cambridge, England), 2021-05, Vol.57 (39), p.4831-4834

2021

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Synthesis of functionalized dispiro[indoline-3,1′-cyclopentane-3′,3″-indolines] via cyclodimerization of 3-phenacylideneoxindolines with benzoylhydrazides and arylhydrazines

Molecular diversity, 2018-02, Vol.22 (1), p.21-36

2018

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HOAc-Mediated Domino Diels–Alder Reaction for Synthesis of Spiro[cyclohexane-1,3′-indolines] in Ionic Liquid [Bmim]Br

ACS omega, 2018-05, Vol.3 (5), p.5406-5416

2018

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TfOH-Catalyzed One-Pot Domino Reaction for Diastereoselective Synthesis of Polysubstituted Tetrahydrospiro[carbazole-1,3′-indoline]s

Journal of organic chemistry, 2017-12, Vol.82 (24), p.13277-13287

2017

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Synthesis of ArCF2X and [18F]Ar-CF3 via Cleavage of the Trifluoromethylsulfonyl Group

Organic letters, 2022-01, Vol.24 (1), p.164-168

2022

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Selective Synthesis of 3‑(9H‑Carbazol-2-yl)indolin-2-ones and Spiro[tetrahydrocarbazole-3,3′-oxindoles] via a HOTf Catalyzed Three-Component Reaction

Journal of organic chemistry, 2018-06, Vol.83 (11), p.5909-5919

2018

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Construction of Tetrahydrospiro[carbazole‐1,2′‐indenes] and Dihydrospiro[carbazole‐1,3′‐indolines] via NH4I Promoted Three‐Component Reaction

ChemistrySelect (Weinheim), 2019-09, Vol.4 (34), p.10100-10103

2019

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Tunable Reduction of Benzyl α,α‐Difluorotriflones: Synthesis of Difluoroarenes and Sodium Aryldifluoromethyl Sufinates and their Applications

ChemistrySelect (Weinheim), 2022-11, Vol.7 (42), p.n/a

2022

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DDQ dehydrogenative Diels-Alder reaction for the synthesis of functionalized spiro[carbazole-1,3′-indolines] and spiro[carbazole-1,5′-pyrimidines]

New journal of chemistry, 2021-08, Vol.45 (34), p.15423-15428

2021

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Selective construction of polycyclic spirooxindoles via a Cu(OTf) 2 /HOTf-catalyzed domino reaction of o-arylalkynylacetophenones and 3-phenacylideneoxindoles

Organic & biomolecular chemistry, 2017-08, Vol.15 (30), p.6353-6357

2017

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One–pot Reaction for the Convenient Synthesis of Functionalized 2‐Oxaspiro[bicyclo[2.2.1]heptane‐2,3′‐indolines]

ChemistrySelect (Weinheim), 2017-01, Vol.2 (1), p.304-308

2017

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Cyclodimerization of 3-phenacylideneoxindolines with amino esters for the synthesis of dispiro[indoline-3,1′-cyclopentane-3′,3″-indolines]

Heterocyclic communications, 2017-08, Vol.23 (4), p.297-303

2017

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Diastereoselective synthesis of dispiro[indoline-3,1′-cyclobutane-2′,3″-indolines] via visible light catalyzed cyclodimerization of 3-phenacylideneoxindoles

Heterocyclic communications, 2016-06, Vol.22 (3), p.151-156

2016

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Stepwise cycloaddition reaction of N-phenacylbenzothiazolium bromides and nitroalkenes for tetrahydro-, dihydro- and benzo[d]pyrrolo[2,1-b]thiazoles

Scientific reports, 2017-04, Vol.7 (1), p.46470-46470, Article 46470

2017

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Synthesis of ArCF 2 X and [ 18 F]Ar-CF 3 via Cleavage of the Trifluoromethylsulfonyl Group

Organic letters, 2022-01, Vol.24 (1), p.164-168

2022

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Selective construction of polycyclic spirooxindoles via a Cu(OTf)2/HOTf-catalyzed domino reaction of o-arylalkynylacetophenones and 3-phenacylideneoxindolesElectronic supplementary information (ESI) available: Experimental procedures, analytical data, and copies of the 1H and 13C NMR spectra, HRMS spectra for all new products (3a-3s and 4o-4v, 6a, G1) (PDF). Single-crystal X-ray data for 3h, 3j, 3k, 3m, 4q, 4r, 4v and G1. CCDC 1523295 (3h), 1523296 (3j), 1523297 (3k), 1523298 (3m), 1523299 (4q),

2017-08

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Chemo-, regio- and stereoselective synthesis of monofluoroalkenes a tandem fluorination-desulfonation sequence

Chemical communications (Cambridge, England), 2021-08, Vol.57 (63), p.782-785

2021

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Base promoted -difluoroolefination of alkyl triflones

Chemical communications (Cambridge, England), 2021-05, Vol.57 (39), p.4831-4834

2021

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Synthesis of functionalized dispiro[indoline-3,1[Formula: see text]-cyclopentane-3[Formula: see text],3[Formula: see text]-indolines] via cyclodimerization of 3-phenacylideneoxindolines with benzoylhydrazides and arylhydrazines

Molecular diversity, 2018-02, Vol.22 (1), p.21-36

2018

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Construction of Tetrahydrospiro[carbazole‐1,2′‐indenes] and Dihydrospiro[carbazole‐1,3′‐indolines] via NH 4 I Promoted Three‐Component Reaction

ChemistrySelect (Weinheim), 2019-09, Vol.4 (34), p.10100-10103

2019

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Risk analysis for a cascade reservoir system using the brittle risk entropy method

Science China. Technological sciences, 2016-06, Vol.59 (6), p.882-887

2016

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Generation of high-energy narrowband 2.05 μm pulses for seeding a Ho：YLF laser

光子学研究：英文版, 2018, Vol.9 (1), p.1-5

2018

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Synthesis of Cyclopropenes and Fluorinated Cyclopropanes via Michael Initiated Ring Closure of Alkyl Triflones

Chemo-, regio- and stereoselective synthesis of monofluoroalkenes via a tandem fluorination–desulfonation sequence

Chameleonic Reactivity of Imidoyl Sulfoxonium Ylides: Access to Functionalized Pyrroles and Dihydro-pyridines

Base promoted gem-difluoroolefination of alkyl triflones

Synthesis of functionalized dispiro[indoline-3,1′-cyclopentane-3′,3″-indolines] via cyclodimerization of 3-phenacylideneoxindolines with benzoylhydrazides and arylhydrazines

HOAc-Mediated Domino Diels–Alder Reaction for Synthesis of Spiro[cyclohexane-1,3′-indolines] in Ionic Liquid [Bmim]Br

TfOH-Catalyzed One-Pot Domino Reaction for Diastereoselective Synthesis of Polysubstituted Tetrahydrospiro[carbazole-1,3′-indoline]s

Synthesis of ArCF2X and [18F]Ar-CF3 via Cleavage of the Trifluoromethylsulfonyl Group

Selective Synthesis of 3‑(9H‑Carbazol-2-yl)indolin-2-ones and Spiro[tetrahydrocarbazole-3,3′-oxindoles] via a HOTf Catalyzed Three-Component Reaction

Construction of Tetrahydrospiro[carbazole‐1,2′‐indenes] and Dihydrospiro[carbazole‐1,3′‐indolines] via NH4I Promoted Three‐Component Reaction

Tunable Reduction of Benzyl α,α‐Difluorotriflones: Synthesis of Difluoroarenes and Sodium Aryldifluoromethyl Sufinates and their Applications

DDQ dehydrogenative Diels-Alder reaction for the synthesis of functionalized spiro[carbazole-1,3′-indolines] and spiro[carbazole-1,5′-pyrimidines]

Selective construction of polycyclic spirooxindoles via a Cu(OTf) 2 /HOTf-catalyzed domino reaction of o-arylalkynylacetophenones and 3-phenacylideneoxindoles

One–pot Reaction for the Convenient Synthesis of Functionalized 2‐Oxaspiro[bicyclo[2.2.1]heptane‐2,3′‐indolines]

Cyclodimerization of 3-phenacylideneoxindolines with amino esters for the synthesis of dispiro[indoline-3,1′-cyclopentane-3′,3″-indolines]

Diastereoselective synthesis of dispiro[indoline-3,1′-cyclobutane-2′,3″-indolines] via visible light catalyzed cyclodimerization of 3-phenacylideneoxindoles

Stepwise cycloaddition reaction of N-phenacylbenzothiazolium bromides and nitroalkenes for tetrahydro-, dihydro- and benzo[d]pyrrolo[2,1-b]thiazoles

Synthesis of ArCF 2 X and [ 18 F]Ar-CF 3 via Cleavage of the Trifluoromethylsulfonyl Group

Chemo-, regio- and stereoselective synthesis of monofluoroalkenes a tandem fluorination-desulfonation sequence

Base promoted -difluoroolefination of alkyl triflones

Synthesis of functionalized dispiro[indoline-3,1[Formula: see text]-cyclopentane-3[Formula: see text],3[Formula: see text]-indolines] via cyclodimerization of 3-phenacylideneoxindolines with benzoylhydrazides and arylhydrazines

Construction of Tetrahydrospiro[carbazole‐1,2′‐indenes] and Dihydrospiro[carbazole‐1,3′‐indolines] via NH 4 I Promoted Three‐Component Reaction

Risk analysis for a cascade reservoir system using the brittle risk entropy method

Generation of high-energy narrowband 2.05 μm pulses for seeding a Ho：YLF laser

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