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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