Publications

2026

J. Am. Chem. Soc. 2026, 148, 37398–37406.
Design of chiral antimony catalyst for ring-opening reaction of epoxides with anilines
Chem. 2026, 12, 103187 (Invited Review Article).
Angew. Chem. Int. Ed. 2026, 65, e3568920.
Asymmetric tellurium-bonding catalysis for Mannich reaction
J. Am. Chem. Soc. 2026, 148, 33959–33969.
Atropisomeric aryl-hydrazone frameworks: discovery and organocatalytic enantioselective construction
Chiral Chem. 2026, 3, 202624.
Chiral Brønsted acid-catalyzed enantioselective synthesis of 3-azabicyclo[3.1.1]heptanes
Catalysts. 2026, 16, 556.
<b>Chiral phosphoric acid-catalyzed hydrolysis of 4H-oxazines for diverse syntheses</b>
Science. 2026, 392, 850-857.
A relay energy transfer paradigm for asymmetric photocatalyzed [4+2] cycloadditions
Sci. China Chem. 2026, 69, 5513-5528.
Chin. J. Chem. 2026, 44, 1865-1875.

2025

Nature. 2025, 647, 897-905.
Controlling pyramidal nitrogen chirality by asymmetric organocatalysis
Angew. Chem. Int. Ed. 2025, e202519340.
Catalytic enantioselective synthesis of axially chiral tetraarylethenes
J. Am. Chem. Soc. 2025, 147, 33879−33887.
Triplet carbene insertion enables modular access to C2-substituted bicyclo[1.1.1]pentanes
Angew. Chem. Int. Ed. 2025, e202511650.
Rational design of an organotellurium chalcogen bonding catalyst for azetidine activation
Org. Chem. Front. 2025, 12, 4126-4150. (Invited Review Article).
Sci. China Chem. 2025, 68, 4973–4983.
Chiral phosphoric acid-catalyzed atroposelective oxidative coupling of carbazoles
Nat. Chem. 2025, 17, 393-402.
Enantioselective synthesis of 2-substituted bicyclo[1.1.1]pentanes via sequential asymmetric imine addition of bicyclo[1.1.0] butanes and skeletal editing
J. Am. Chem. Soc. 2025, 147, 3450-3458.
Organocatalytic activation of alkynes enabled remote control of atroposelectivity via vinylidene
ACS Cent. Sci. 2025, 11, 248-260.
Nickel(II) catalyzed atroposelective aerobic oxidative aryl–aryl cross-coupling
Angew. Chem. Int. Ed. 2025, 64, e202422951.
Organocatalytic asymmetric construction and application of axially chiral spiro-bisindoles

2024

Angew. Chem. Int. Ed. 2024, 63, e202412508.
Design of stable chiral aminosulfonium ylides and their catalytic asymmetric synthesis
Chin. J. Chem. 2024, 42, 2656-2667. (Invited Review Article).
J. Am. Chem. Soc. 2024, 146, 19137-19145.
Enantioselective construction of anthracenylidene-based axial chirality by asymmetric Heck reaction
Nat. Catal. 2024, 7, 483-498. (Invited Review Article).
Nat. Catal. 2024, 7, 185-194.
Organocatalytic olefin C–H functionalization for enantioselective synthesis of atropisomeric 1,3-dienes
Nat. Chem. 2024, 16, 408-416.
Organocatalytic aromatization-promoted umpolung reaction of imines
Chin. J. Chem. 2024, 42, 731-735.
Atroposelective synthesis of 2-arylindoles via chiral phosphoric acid-catalyzed direct amination of indoles

2023

J. Am. Chem. Soc. 2023, 145, 21152-21158.
Enantioselective synthesis of chiral cyclobutenes enabled by Brønsted acid-catalyzed isomerization of BCBs
J. Am. Chem. Soc. 2023, 145, 20646-20654.
Organocatalytic Si-CAryl bond functionalization enabled atroposelective synthesis of axially chiral biaryl siloxanes
Angew. Chem. Int. Ed. 2023, 62, e202309272.
Synthesis of axially chiral QUINAP derivatives by ketone-catalyzed enantioselective oxidation
Chem. Rec. 2023, e202300147 (Invited Review Article).
Angew. Chem. Int. Ed. 2023, 62, e202303128.
Organocatalytic atroposelective cross-coupling of 1-azonaphthalenes and 2-naphthols
Nat. Chem. 2023, 15, 647-657.
Modular enantioselective access to β-amino amides by Brønsted acid-catalysed multicomponent reaction
Chem. 2023, 9, 1495-1504.
Catalytic enantioselective synthesis of chiral sulfonium ylides with S-stereogenic center. 
Chem. Synth. 2023, 3, 11.
Enantioselective synthesis of 3-arylindole atropisomers via organocatalytic indolization of iminoquinones
Chem. Sci. 2023, 14, 2330-2335.
Enantioselective construction of triaryl-substituted all-carbon quaternary stereocenters via organocatalytic arylation of oxindoles with azonaphthalenes. Chem. Sci. 2023, 14, 2330-2335
Nat. Synth. 2023, 2, 83-85 (Invited News & Views).
Angew. Chem. Int. Ed. 2023, 62, e202215820.
Asymmetric hydrophosphinylation of alkynes: facile access to axially chiral styrene-phosphines
Chin. J. Chem. 2023, 41, 685-694 (Invited Review Article).
Angew. Chem. Int. Ed. 2023, 62, e202213914.
Phosphoric acid-catalyzed enantioselective synthesis of axially chiral anthrone-based compounds

2022

Chem. Catal. 2022, 2, 2802–2839 (Invited Preview).
Synlett. 2022, 33, 1991-2003 (Invited Review Article).
Acc. Chem. Res. 2022, 55, 2920-2937 (Invited Personal Account).
Angew. Chem. Int. Ed. 2022, 61, e202211211.
Asymmetric construction of aryl-alkene axis by palladium-catalyzed Suzuki–Miyaura coupling reaction
Chem. 2022, 8, 2529-2541.
Discovery and organocatalytic enantioselective construction of axially chiral cyclohexadienylidene skeletons. Chem. 2022, 8, 2529-2541
Sci. China Chem. 2022, 65, 1142-1148.
Asymmetric synthesis of binaphthyls through photocatalytic cross
coupling and organocatalytic kinetic resolution
Tetrahedron Chem. 2022, 1, 100009.
Chem. Commun. 2022, 58, 4392-4395.
Direct arylation of N-heterocycles enabled by photoredox catalysis
Chem. Commun. 2022, 58, 1613-1616.
Facile synthesis of N-aryl phenothiazines and phenoxazines via Brønsted acid catalyzed C–H amination of arenes

2021

Angew. Chem. Int. Ed. 2021, 60, 24888-24893.
Nitrosobenzene-enabled chiral phosphoric acid catalyzed enantioselective construction of atropisomeric N-arylbenzimidazoles
J. Am. Chem. Soc. 2021, 143, 12924-12929.
Chiral phosphoric acid-catalyzed remote control of axial chirality at boron–carbon bond
Nat. Catal. 2021, 4, 692-702.
Urea group-directed organocatalytic asymmetric versatile dihalogenation of alkenes and alkynes
Nat. Chem. 2021, 13, 982-991.
Organocatalyst-controlled site-selective arene C–H functionalization
Chem. Com. 2021, 57, 8512-8515.
Electrochemical phenothiazination of naphthylamines and its application in photocatalysis
Sci. China Chem. 2021, 64, 1515-1521.
Synthesis of structurally diversified BINOLs and NOBINs via palladium-catalyzed C-H arylation with diazoquinones
Molecules. 2021, 26, 3223.
Copper-catalyzed synthesis of axially chiral biaryls with diaryliodonium salts as arylation reagents
J. Am. Chem. Soc. 2021, 143, 6382-6387.
Asymmetric pnictogen-bonding catalysis: transfer hydrogenation by a chiral antimony(V) cation/anion pair
Nat. Commun. 2021, 12, 2384.
Metal-free oxidative cross-coupling enabled practical synthesis of atropisomeric QUINOL and its derivatives
Chem. Rev. 2021, 121, 4805-4902 (Invited Review Article).
Chin. J. Chem. 2021, 39, 1787-1796 (Invited Personal Account).

2020

Angew. Chem. Int. Ed. 2020, 59, 23077-23082.
Design and atroposelective construction of IAN analogues by organocatalytic asymmetric heteroannulation of alkynes
Nat. Commun. 2020, 11, 3786 (Invited Comment).
Chin. J. Chem. 2020, 38, 1503-1514.
Direct construction of NOBINs via domino arylation and sigmatropic rearrangement reactions
Chem. 2020, 6, 2046-2059.
DFT-guided phosphoric-acid-catalyzed atroposelective arene functionalization of nitrosonaphthalene
Angew. Chem. Int. Ed. 2020, 59, 11374-11378.
Organocatalytic enantioselective synthesis of atropisomeric aryl-p-quinones: platform molecules for diversity-oriented synthesis of biaryldiols
J. Am. Chem. Soc. 2020, 142, 7322-7327.
Michael reaction inspired atroposelective construction of axially chiral biaryls
Angew. Chem. Int. Ed. 2020, 59, 6775-6779.
Chiral phosphoric acid catalyzed atroposelective C-H amination of arenes
Chin. J. Chem. . 2020, 38, 213-214 (Invited Emerging Topic).
Sci. China Chem. 2020, 63, 47-54.
Enantioselective three-component Ugi reaction catalyzed by chiral phosphoric acid

2019

Nat. Commun. 2019, 10, 4268.
Organocatalytic atroposelective construction of axially chiral arylquinones
Angew. Chem. Int. Ed. 2019, 58, 13443-13447.
Asymmetric construction of axially chiral 2-arylpyrroles by chirality transfer of atropisomeric alkenes
Org. Lett. 2019, 21, 6000-6004.
Atroposelective construction of arylindoles by chiral phosphoric acid-catalyzed cross-coupling of indoles and quinones
Nat. Catal. 2019, 2, 504-513.
Rational design, enantioselective synthesis and catalytic applications of axially chiral EBINOLs
Nat. Catal. 2019, 2, 314-323.
Asymmetric construction of atropisomeric biaryls via a redox neutral cross-coupling strategy
Nat. Commun. 2019, 10, 566.
Phosphoric acid-catalyzed atroposelective construction of axially chiral arylpyrroles
Tetrahedron. 2019, 75, 1689-1696.
Organocatalytic double arylation of 3-isothiocyanato oxindoles: Stereocontrolled synthesis of complex spirooxindoles

2018

Chin. J. Chem. 2018, 36, 1182-1186.
Stereoselective construction of complex spirooxindoles via bisthiourea catalyzed three-component reactions
Org. Lett. 2018, 20, 6022-6025.
Remote control of axial chirality: synthesis of spirooxindole–urazoles via desymmetrization of ATAD
Science. 2018, 361, eaas8707.
Asymmetric phosphoric acid–catalyzed four-component Ugi reaction
Acc. Chem. Res. 2018, 51, 534-547 (Invited Personal Account).
Tetrahedron Lett. 2018, 59, 473-486 (Invited Review).
Nat. Chem. 2018, 10, 58-64.
Organocatalytic asymmetric arylation of indoles enabled by azo groups

2017

Angew. Chem. Int. Ed. 2017, 56, 16308-16311.
Organocatalytic atroposelective arylation of 2-naphthylamines as a practical approach to axially chiral biaryl amino alcohols
Nat. Commun. 2017, 8, 15489.
Brønsted Acid-Catalysed Enantio-selective Construction of Axially Chiral Arylquinazolinones
Nat. Commun. 2017, 8, 15238.
Organocatalytic atroposelective synthesis of axially chiral styrenes
J. Am. Chem. Soc. 2017, 139, 1714-1717.
Highly atroposelective synthesis of arylpyrroles by catalytic asymmetric Paal-Knorr reaction

2016

Nat. Commun. 2016, 7, 13852.
J. Am. Chem. Soc. 2016, 138, 16561-16566.
Phosphoric acid-catalyzed asymmetric synthesis of SPINOL derivatives
Angew. Chem. Int. Ed. 2016, 55, 11834-11839.
Construction of tropane derivatives by organocatalytic asymmetric dearomatization of isoquinolines
ACS Catal. 2016, 6, 6182-6190.
J. Am. Chem. Soc. 2016, 138, 9357-9360.
Nat. Commun. 2016, 7, 10677.
Discovery and enantiocontrol of axially chiral urazoles via organocatalytic tyrosine click reaction
Chem. Commun. 2016, 52, 9052-9055.
Org. Chem. Front. 2016, 3, 324-329.

2015

J. Am. Chem. Soc. 2015, 137, 15062-15065.
Atroposelective synthesis of axially chiral biaryldiols via organocatalytic arylation of 2‑naphthols
J. Am. Chem. Soc. 2015, 137, 14039-14042.
Phosphoric acid-catalyzed asymmetric classic Passerini reaction
Angew. Chem. Int. Ed. 2015, 54, 9528-9532.
Asymmetric synthesis of axially chiral isoquinolones: nickel-catalyzed denitrogenative transannulation
Angew. Chem. Int. Ed. 2015, 54, 9409-9413.
Asymmetric construction of spirooxindoles by organocatalytic multicomponent reactions using diazooxindoles
Angew. Chem. Int. Ed. 2015, 54, 7847-7851.
ACS Catal. 2015, 5, 2826-2831.
Org. Lett. 2015, 17, 1589-1592.
Chem. Eur. J. 2015, 21, 6718-6722.
Angew. Chem. Int. Ed. 2015, 54, 4041-4045.
Adv. Synth. Catal. 2015, 357, 569-575.

2014

Org. Lett. 2014, 16, 6032-6035.
Angew. Chem. Int. Ed. 2014, 53, 11890-11894.
J. Org. Chem. 2014, 79, 7084-7092.
Org. Lett. 2014, 16, 2192-2195.
Angew. Chem. Int. Ed. 2014, 53, 3684-3687.
Highly enantioselective kinetic resolution of axially chiral BINAM derivatives catalyzed by a Brønsted acid
Org. Lett. 2014, 16, 1000-1003.
ACS Catal. 2014, 4, 743-762 (Invited Review Article).
Chem. Eur. J. 2014, 20, 1332-1340.
Org. Lett. 2014, 16, 504-507.
2014.

2013

Org. Lett. 2013, 15, 2958.
Angew. Chem. Int. Ed. 2013, 52, 9261.

2012

Org. Lett. 2012, 14, 1834.
Chem. Eur. J. 2012, 18, 63.
Org. Lett. 2012, 14, 1858.
Angew. Chem. Int. Ed. 2012, 51, 12538.
Angew. Chem. Int. Ed. 2012, 51, 5381.

2011

Nature Chem. 2011, 3, 473.
J. Am. Chem. Soc. 2011, 133, 4672.
J. Am. Chem. Soc. 2011, 133, 12354.

2010

Org. Lett. 2010, 12, 5402.
Org. Lett. 2010, 12, 2414.
Chem. Commun. 2010, 46, 2504.
Org. Lett. 2010, 12, 2682.
Chem. Commun. 2010, 46, 7611.
Chem. Eur. J. 2010, 16, 3842.

2009

L. 2009, 11, 543.
Org. Chem. 2009, 74, 1744.
J. Am. Chem. Soc. 2009, 131, 4562.
L. 2009, 19, 3915.
Org. Lett. 2009, 11, 1927.
Chem. Commun. 2009, 12, 779.
Angew. Chem. Int. Ed. 2009, 48, 758.

2008

Org. Lett. 2008, 10, 3489.
Org. Lett. 2008, 10, 4585.
Org. Lett. 2008, 10, 3425.
Angew. Chem. Int. Ed. 2008, 47, 10187.
Org. Lett. 2008, 10, 2437.
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