Kumar Dilip Ashtekar, Hadi Gholami, Mehdi Moemeni, Ankush Chakraborty, Lindsey Kiiskila, Xinliang Ding, Edmond Toma, Christopher Rahn and Babak Borhan

Angew Chem Int Ed, 2022, 61
DOI: 10.1002/anie.202115173

Stereoselective Halocyclization of Alkenes With N‐Acyl Hemiaminal Nucleophiles

Na Liu, Hao‐Yuan Wang, Wei Zhang, Zhi‐Hong Jia, Ilia A. Guzei, Hua‐dong Xu and Weiping Tang

Chirality, 2013, 25, 805
DOI: 10.1002/chir.22219

Catalytic Enantioselective Iodoetherification of Oximes

Chandra Bhushan Tripathi and Santanu Mukherjee

Angew Chem Int Ed, 2013, 52, 8450
DOI: 10.1002/anie.201304173

Synthesis of chiral butenolides using amino-thiocarbamate-catalyzed asymmetric bromolactonization

Chong Kiat Tan, Jun Cheng Er and Ying-Yeung Yeung

Tetrahedron Letters, 2014, 55, 1243
DOI: 10.1016/j.tetlet.2014.01.009

Intramolecular Alkene Electrophilic Bromination Initiated ipso-Bromocyclization for the Synthesis of Functionalized Azaspirocyclohexadienones

Qin Yin and Shu-Li You

Org. Lett., 2012, 14, 3526
DOI: 10.1021/ol301531z

Stereoselective Electrophilic Cyclization

Akira Sakakura and Kazuaki Ishihara

The Chemical Record, 2015, 15, 728
DOI: 10.1002/tcr.201500005

Kinetic Resolution of Racemic Carboxylic Acids through Asymmetric Protolactonization Promoted by Chiral Phosphonous Acid Diester

Masayuki Sakuma, Akira Sakakura and Kazuaki Ishihara

Org. Lett., 2013, 15, 2838
DOI: 10.1021/ol401313d

Catalytic Desymmetrization of Cyclohexadienes by Asymmetric Bromolactonization

Kazutada Ikeuchi, Shunsuke Ido, Satoshi Yoshimura, Tomohiro Asakawa, Makoto Inai, Yoshitaka Hamashima and Toshiyuki Kan

Org. Lett., 2012, 14, 6016
DOI: 10.1021/ol302908a

Catalytic, Asymmetric Halofunctionalization of Alkenes—A Critical Perspective

Scott E. Denmark, William E. Kuester and Matthew T. Burk

Angew Chem Int Ed, 2012, 51, 10938
DOI: 10.1002/anie.201204347

Chiral‐Amine‐Catalyzed Asymmetric Bromocyclization of Tryptamine Derivatives

Quan Cai, Qin Yin and Shu‐Li You

Asian J Org Chem, 2014, 3, 408
DOI: 10.1002/ajoc.201300146

Divergent synthesis of L-685,458 and its analogues involving one-pot intramolecular tandem sequence reaction

Chang-Mei Si, Zhuo-Ya Mao, Zhu Zhou, Zhen-Ting Du and Bang-Guo Wei

Tetrahedron, 2015, 71, 9396
DOI: 10.1016/j.tet.2015.10.059

Catalytic Asymmetric Synthesis of Butenolides and Butyrolactones

Bin Mao, Martín Fañanás-Mastral and Ben L. Feringa

Chem. Rev., 2017, 117, 10502
DOI: 10.1021/acs.chemrev.7b00151

Oxyamination of Unactivated Alkenes with Electron-Rich Amines and Acids via a Catalytic Triiodide Intermediate

Fan Wu, Jeewani P. Ariyarathna, Nur-E Alom, Navdeep Kaur and Wei Li

Org. Lett., 2020, 22, 884
DOI: 10.1021/acs.orglett.9b04432

Highly Stereoselective Intermolecular Haloetherification and Haloesterification of Allyl Amides

Bardia Soltanzadeh, Arvind Jaganathan, Richard J. Staples and Babak Borhan

Angew Chem Int Ed, 2015, 54, 9517
DOI: 10.1002/anie.201502341

Efficient Medium Ring Size Bromolactonization Using a Sulfur-Based Zwitterionic Organocatalyst

Yi An Cheng, Tao Chen, Chong Kiat Tan, Jun Jie Heng and Ying-Yeung Yeung

J. Am. Chem. Soc., 2012, 134, 16492
DOI: 10.1021/ja307210n

Enantioselective Syntheses of α‐exo‐Methylene‐Lactones via Organocatalytic Halolactonization

Wei Wang, Haoquan He, Min Gan, Haitao Wang, Yuqiang Wang and Xiaojian Jiang

Adv Synth Catal, 2019, 361, 4797
DOI: 10.1002/adsc.201900728

Catalytic and enantioselective bromoetherification of olefinic 1,3-diols: mechanistic insight

Zhihai Ke, Chong Kiat Tan, Yi Liu, Keefe Guang Zhi Lee and Ying-Yeung Yeung

Tetrahedron, 2016, 72, 2683
DOI: 10.1016/j.tet.2015.09.016

Mechanistic Investigation of an Organocatalytic Bromocyclization of O‐Allyl Carbamates

Francisco Wanderson Moreira Ribeiro, Jullyane Emi Matsushima, Guilherme Obeid, Elisângela Vinhato, Alessandro Rodrigues and Thiago Carita Correra

ChemCatChem, 2025, 17
DOI: 10.1002/cctc.202402004

Divergent syntheses of L-733, 060 and CP-122721 from functionalized pieridinones made by one-pot tandem cyclization

Yi-Wen Liu, Zhuo-Ya Mao, Rui-Jun Ma, Jia-Hang Yan, Chang-Mei Si and Bang-Guo Wei

Tetrahedron, 2017, 73, 2100
DOI: 10.1016/j.tet.2017.02.057

Alkyl-O-(2,4-dicholorobenzoyl)carbamothioates: A two-step, “one-pot” synthesis, structural investigation by experimental and computational methods and molecular docking study

N. Sampath, N. Jeeva and N. Gunasekaran

Journal of Molecular Structure, 2025, 1346, 143106
DOI: 10.1016/j.molstruc.2025.143106

Desymmetrization of Diolefinic Diols by Enantioselective Amino‐thiocarbamate‐Catalyzed Bromoetherification: Synthesis of Chiral Spirocycles

Daniel Weiliang Tay, Gulice Y. C. Leung and Ying‐Yeung Yeung

Angewandte Chemie, 2014, 126, 5261
DOI: 10.1002/ange.201310136

Highly Stereoselective Intermolecular Haloetherification and Haloesterification of Allyl Amides

Bardia Soltanzadeh, Arvind Jaganathan, Richard J. Staples and Babak Borhan

Angewandte Chemie, 2015, 127, 9653
DOI: 10.1002/ange.201502341

Asymmetric Brominative Dearomatization of Naphthols Catalyzed by Chiral Copper Complexes

Yi‐Feng Wang, Juan‐Juan Shao, Biao Wang, Ming‐Ming Chu, Suo‐Suo Qi, Xiao‐Hua Du and Dan‐Qian Xu

Adv Synth Catal, 2018, 360, 2285
DOI: 10.1002/adsc.201800067

Carbamate‐Catalyzed Enantioselective Bromolactamization

Yi An Cheng, Wesley Zongrong Yu and Ying‐Yeung Yeung

Angewandte Chemie, 2015, 127, 12270
DOI: 10.1002/ange.201504724

Kinetic Resolution of β-Substituted Olefinic Carboxylic Acids by Asymmetric Bromolactonization

Kenichi Murai, Tomoyo Matsushita, Akira Nakamura, Norimichi Hyogo, Junki Nakajima and Hiromichi Fujioka

Org. Lett., 2013, 15, 2526
DOI: 10.1021/ol401007u

Lewis Base Catalyzed Stereo‐ and Regioselective Bromocyclization

Matthew H. Gieuw, Zhihai Ke and Ying‐Yeung Yeung

The Chemical Record, 2017, 17, 287
DOI: 10.1002/tcr.201600088

Catalytic enantioselective 5-endo-bromocycloetherification of unactivated cyclic alkenes

Haoran Xiong, Kei Yoshida, Kosuke Okada, Hirofumi Ueda and Hidetoshi Tokuyama

Tetrahedron Letters, 2022, 101, 153906
DOI: 10.1016/j.tetlet.2022.153906

Catalytic Asymmetric Iodoesterification of Simple Alkenes

Takayoshi Arai, Kodai Horigane, Takumi K. Suzuki, Ryosuke Itoh and Masahiro Yamanaka

Angewandte Chemie, 2020, 132, 12780
DOI: 10.1002/ange.202003886

Mechanistic Insights into the Origin of Stereoselectivity in an Asymmetric Chlorolactonization Catalyzed by (DHQD)2PHAL

Roozbeh Yousefi, Aritra Sarkar, Kumar Dilip Ashtekar, Daniel C. Whitehead, Tayeb Kakeshpour, Daniel Holmes, Paul Reed, James E. Jackson and Babak Borhan

J. Am. Chem. Soc., 2020, 142, 7179
DOI: 10.1021/jacs.0c01830

Catalytic Enantioselective Bromoaminocyclization and Bromocycloetherification

Haitao Wang, Haijing Zhong, Xi Xu, Wei Xu and Xiaojian Jiang

Adv Synth Catal, 2020, 362, 5358
DOI: 10.1002/adsc.202000845

Divergent Access to (1,1) and (1,2)‐Azidolactones from Alkenes using Hypervalent Iodine Reagents

Sébastien Alazet, Franck Le Vaillant, Stefano Nicolai, Thibaut Courant and Jerome Waser

Chemistry A European J, 2017, 23, 9501
DOI: 10.1002/chem.201702599

Enantioselective Haloetherifications Catalyzed by 1,1′‐Bi‐2‐naphthol (BINOL) Phosphates: From Symmetrical Alkenediols to Simple Alkenols

Christian H. Müller, Christian Rösner and Ulrich Hennecke

Chemistry An Asian Journal, 2014, 9, 2162
DOI: 10.1002/asia.201402229

Divergent Synthesis of α,α‐Dihaloamides through α,α‐Dihalogenation of β‐Oxo Amides by Using N‐Halosuccinimides

Jia Wang, Hongtao Li, Dingyuan Zhang, Peng Huang, Zikun Wang, Rui Zhang, Yongjiu Liang and Dewen Dong

Eur J Org Chem, 2013, 2013, 5376
DOI: 10.1002/ejoc.201300341

Exploration of the Bis(thio)urea‐Catalyzed Atropselective Synthesis of Marinopyrrole A

Maciej Stodulski, Stefanie V. Kohlhepp, Gerhard Raabe and Tanja Gulder

Eur J Org Chem, 2016, 2016, 2170
DOI: 10.1002/ejoc.201600147

Diastereoconvergent Synthesis of trans-5-Hydroxy-6-Substituted-2-Piperidinones by Addition–Cyclization–Deprotection Process

Chang-Mei Si, Wei Huang, Zhen-Ting Du, Bang-Guo Wei and Guo-Qiang Lin

Org. Lett., 2014, 16, 4328
DOI: 10.1021/ol5020812

Diastereoselective approach to trans -5-hydroxy-6-substitutedethanone-2-piperidinones: Scalable syntheses of (+)-febrifugine and (+)-halofuginone

Chen Wang, Yi-Wen Liu, Zhu Zhou, Chang-Mei Si, Xun Sun and Bang-Guo Wei

Tetrahedron, 2018, 74, 2158
DOI: 10.1016/j.tet.2018.03.022

Use of Bromine and Bromo-Organic Compounds in Organic Synthesis

Indranirekha Saikia, Arun Jyoti Borah and Prodeep Phukan

Chem. Rev., 2016, 116, 6837
DOI: 10.1021/acs.chemrev.5b00400

Divergent Method to trans-5-Hydroxy-6-alkynyl/alkenyl-2-piperidinones: Syntheses of (−)-Epiquinamide and (+)-Swainsonine

Chang-Mei Si, Zhuo-Ya Mao, Han-Qing Dong, Zhen-Ting Du, Bang-Guo Wei and Guo-Qiang Lin

J. Org. Chem., 2015, 80, 5824
DOI: 10.1021/acs.joc.5b00803

Enantioselective Chlorocyclization of Olefinic Amides with 1,3-Dichloro- 5, 5-Dimethylhydantoin (DCDMH) Catalyzed by (DHQD)2PHAL

Qingjun Zhou, Chao Guo, Xiwang Li, Pei He, Guichun Yang and Chune Dong

Wuhan Univ. J. Nat. Sci., 2018, 23, 259
DOI: 10.1007/s11859-018-1319-9

Cooperative Activation with Chiral Nucleophilic Catalysts and N‐Haloimides: Enantioselective Iodolactonization of 4‐Arylmethyl‐4‐pentenoic Acids

Hidefumi Nakatsuji, Yasuhiro Sawamura, Akira Sakakura and Kazuaki Ishihara

Angewandte Chemie, 2014, 126, 7094
DOI: 10.1002/ange.201400946

Catalytic Asymmetric Iodoesterification of Simple Alkenes

Takayoshi Arai, Kodai Horigane, Takumi K. Suzuki, Ryosuke Itoh and Masahiro Yamanaka

Angew Chem Int Ed, 2020, 59, 12680
DOI: 10.1002/anie.202003886

Cinchona-Alkaloids Based Isoselenazolones: Synthesis and Their Catalytic Reactivity in Asymmetric Bromolactonization of Alkenoic Acid

Shah Jaimin Balkrishna, Shailesh Kumar, Amit Kumar, Piyush Panini and Sangit Kumar

Proc. Natl. Acad. Sci., India, Sect. A Phys. Sci., 2016, 86, 589
DOI: 10.1007/s40010-016-0306-9

Enantioselective Organocatalytic Iodination-Initiated Wagner–Meerwein Rearrangement

Fedor Romanov-Michailidis, Laure Guénée and Alexandre Alexakis

Org. Lett., 2013, 15, 5890
DOI: 10.1021/ol402981z

Enantioselective Bromolactonization of Deactivated Olefinic Acids

Xiaojian Jiang, Shenghui Liu, Si Yang, Mei Jing, Lipeng Xu, Pei Yu, Yuqiang Wang and Ying-Yeung Yeung

Org. Lett., 2018, 20, 3259
DOI: 10.1021/acs.orglett.8b01125

Coordination of O-Propyl-N-phenylthiocarbamate to HgI2 and the Crystallographic Characterization of an Anilinium Chloride Thiocarbamate Adduct

Wafa Arar, Nuri Ekici, Michael Knorr, Isabelle Jourdain, Carsten Strohmann and Jan-Lukas Kirchhoff

Molbank, 2024, 2024, M1923
DOI: 10.3390/M1923

Catalytic Enantioselective Chlorofunctionalizations of N-Substituted Amides Using In Situ Generated HOCl as Hydrogen Bond Source

Tengbo Ding, Liang Long, Mei-Jie Yuan, Wei Xu, Sze-Yung Wong, Hao Gao, Yong-Heng Wang, Ying-Yeung Yeung and Xiaojian Jiang

J. Am. Chem. Soc., 2025, 147, 16225
DOI: 10.1021/jacs.5c01224

Lewis Basic Selenium Catalyzed Chloroamidation of Olefins Using Nitriles as the Nucleophiles

Daniel Weiliang Tay, Ivan Tan Tsoi, Jun Cheng Er, Gulice Yiu Chung Leung and Ying-Yeung Yeung

Org. Lett., 2013, 15, 1310
DOI: 10.1021/ol400249x

Recent Progress in Organocatalytic Asymmetric Halocyclization

Hiromichi Fujioka and Kenichi Murai

HETEROCYCLES, 2013, 87, 763
DOI: 10.3987/REV-12-762

Enantioselective 6-exo-Bromoaminocyclization of Homoallylic N-Tosylcarbamates Catalyzed by a Novel Monophosphine-Sc(OTf)3 Complex

Weigang Liu, Hongjie Pan, Hua Tian and Yian Shi

Org. Lett., 2015, 17, 3956
DOI: 10.1021/acs.orglett.5b01779

Bioinspired Total Synthesis of (+)-α-Tocopherol

Jiaxin Cheng, Zhigang Liu, Ding Liu, Pei Tang and Fen-Er Chen

Org. Lett., 2025, 27, 8618
DOI: 10.1021/acs.orglett.5c02571

Enantioselective Bromolactonization Using an S‐Alkyl Thiocarbamate Catalyst

Xiaojian Jiang, Chong Kiat Tan, Ling Zhou and Ying‐Yeung Yeung

Angew Chem Int Ed, 2012, 51, 7771
DOI: 10.1002/anie.201202079

Katalytische asymmetrische Halogenfunktionalisierung von Alkenen – eine kritische Betrachtung

Scott E. Denmark, William E. Kuester and Matthew T. Burk

Angewandte Chemie, 2012, 124, 11098
DOI: 10.1002/ange.201204347

Carboxylic Acids as Building Blocks in Catalytic Asymmetric Reactions

Nilanjana Majumdar

ACS Catal., 2022, 12, 8291
DOI: 10.1021/acscatal.2c02410

Total synthesis of natural products using a desymmetrization strategy

Makoto Inai, Tomohiro Asakawa and Toshiyuki Kan

Tetrahedron Letters, 2018, 59, 1343
DOI: 10.1016/j.tetlet.2018.02.059

Enantioselective Bromolactonization Using an S‐Alkyl Thiocarbamate Catalyst

Xiaojian Jiang, Chong Kiat Tan, Ling Zhou and Ying‐Yeung Yeung

Angewandte Chemie, 2012, 124, 7891
DOI: 10.1002/ange.201202079

Computational study on the mechanism of uncatalyzed and selenium-based catalyzed bromolactonization

Chuanzhi Sun, Xiaodan He, Wenjuan Wang, Guohong Chu, Shuxiang Zhang and Dezhan Chen

Computational and Theoretical Chemistry, 2014, 1046, 49
DOI: 10.1016/j.comptc.2014.07.014

Cooperative Activation with Chiral Nucleophilic Catalysts and N‐Haloimides: Enantioselective Iodolactonization of 4‐Arylmethyl‐4‐pentenoic Acids

Hidefumi Nakatsuji, Yasuhiro Sawamura, Akira Sakakura and Kazuaki Ishihara

Angew Chem Int Ed, 2014, 53, 6974
DOI: 10.1002/anie.201400946

Halogen-Induced Controllable Cyclizations as Diverse Heterocycle Synthetic Strategy

Hideyasu China, Ravi Kumar, Kotaro Kikushima and Toshifumi Dohi

Molecules, 2020, 25, 6007
DOI: 10.3390/molecules25246007

3‐Isothiocyanato Oxindoles Serving as Powerful and Versatile Precursors to Structurally Diverse Dispirocyclic Thiopyrrolidineoxindoles through a Cascade Michael/Cyclization Process with Amino‐Thiocarbamate Catalysts

Wen‐Yong Han, Shi‐Wu Li, Zhi‐Jun Wu, Xiao‐Mei Zhang and Wei‐Cheng Yuan

Chemistry A European J, 2013, 19, 5551
DOI: 10.1002/chem.201300206

Catalytic Enantioselective Halocyclizations to Access Benzoxazepinones and Benzoxazecinones

Xiaojian Jiang, Xi Xu, Wei Xu, Pei Yu and Ying-Yeung Yeung

Org. Lett., 2021, 23, 6316
DOI: 10.1021/acs.orglett.1c02117

Enantioselective Iodolactonization of Disubstituted Olefinic Acids Using a Bifunctional Catalyst

Chao Fang, Daniel H. Paull, J. Caleb Hethcox, Christopher R. Shugrue and Stephen F. Martin

Org. Lett., 2012, 14, 6290
DOI: 10.1021/ol3030555

Synthesis, crystal structures and biological activities of halogeno-(O-alkylphenylcarbamothioate)bis(triarylphosphine)copper(I) complexes

Wafa Arar, Ridha Ben Ali, Michèle Véronique El May, Abderrahim Khatyr, Isabelle Jourdain, Michael Knorr, Lukas Brieger, Rebecca Scheel, Carsten Strohmann, Asma Chaker and Azaiez Ben Akacha

Journal of Molecular Structure, 2023, 1284, 135370
DOI: 10.1016/j.molstruc.2023.135370

A Catalyst-Controlled Enantiodivergent Bromolactonization

Yuk-Cheung Chan, Xinyan Wang, Ying-Pong Lam, Jonathan Wong, Ying-Lung Steve Tse and Ying-Yeung Yeung

J. Am. Chem. Soc., 2021, 143, 12745
DOI: 10.1021/jacs.1c05680

Bifunctional Catalyst Promotes Highly Enantioselective Bromolactonizations To Generate Stereogenic C–Br Bonds

Daniel H. Paull, Chao Fang, James R. Donald, Andrew D. Pansick and Stephen F. Martin

J. Am. Chem. Soc., 2012, 134, 11128
DOI: 10.1021/ja305117m

Synthesis of Chromenoisoxazolidines from Substituted Salicylic Nitrones via Visible-Light Photocatalysis

Graham Haun, Alyson N. Paneque, David W. Almond, Brooke E. Austin and Gustavo Moura-Letts

Org. Lett., 2019, 21, 1388
DOI: 10.1021/acs.orglett.9b00097

Enantioselective Halogenative Semi‐Pinacol Rearrangement: Extension of Substrate Scope and Mechanistic Investigations

Fedor Romanov‐Michailidis, Maria Romanova‐Michaelides, Marion Pupier and Alexandre Alexakis

Chemistry A European J, 2015, 21, 5561
DOI: 10.1002/chem.201406133

Construction of Sulfonyl Phthalides via Copper-Catalyzed Oxysulfonylation of 2-Vinylbenzoic Acids with Sodium Sulfinates

Yan-Shi Xiong, Bin Zhang, Yang Yu, Jiang Weng and Gui Lu

J. Org. Chem., 2019, 84, 13465
DOI: 10.1021/acs.joc.9b01646

Solvent‐Dependent Enantiodivergence in the Chlorocyclization of Unsaturated Carbamates

Atefeh Garzan, Arvind Jaganathan, Nastaran Salehi Marzijarani, Roozbeh Yousefi, Daniel C. Whitehead, James E. Jackson and Babak Borhan

Chemistry A European J, 2013, 19, 9015
DOI: 10.1002/chem.201300189

Divergent Synthesis of α,γ-Disubstituted γ-Butyrolactones through Diastereoselective Bromolactonization with Alkali Metal Bromide: Asymmetric Total Synthesis of (+)-Dubiusamine C

Katsuhiko Moriyama, Toru Sugiue, Chihiro Nishinohara and Hideo Togo

J. Org. Chem., 2015, 80, 9132
DOI: 10.1021/acs.joc.5b01497

A Mechanistically Inspired Halenium Ion Initiated Spiroketalization: Entry to Mono‐ and Dibromospiroketals

Kumar Dilip Ashtekar, Hadi Gholami, Mehdi Moemeni, Ankush Chakraborty, Lindsey Kiiskila, Xinliang Ding, Edmond Toma, Christopher Rahn and Babak Borhan

Angewandte Chemie, 2022, 134
DOI: 10.1002/ange.202115173

Catalytic Enantioselective Iodoetherification of Oximes

Chandra Bhushan Tripathi and Santanu Mukherjee

Angewandte Chemie, 2013, 125, 8608
DOI: 10.1002/ange.201304173

Kinetic Resolution of Unsaturated Amides in a Chlorocyclization Reaction: Concomitant Enantiomer Differentiation and Face Selective Alkene Chlorination by a Single Catalyst

Arvind Jaganathan, Richard J. Staples and Babak Borhan

J. Am. Chem. Soc., 2013, 135, 14806
DOI: 10.1021/ja407241d

Synthesis of (+)-Disparlure via Enantioselective Iodolactonization

Daniel W. Klosowski and Stephen F. Martin

Org. Lett., 2018, 20, 1269
DOI: 10.1021/acs.orglett.7b03911

Catalytic enantioselective bromolactonization of alkenoic acids in the presence of palladium complexes

Hyun Joo Lee and Dae Young Kim

Tetrahedron Letters, 2012, 53, 6984
DOI: 10.1016/j.tetlet.2012.10.051

Indium chloride mediated chlorolactonization: construction of chlorinated lactone fragments

Hideki Abe, Naoki Fukazawa, Toyoharu Kobayashi and Hisanaka Ito

Tetrahedron, 2013, 69, 2519
DOI: 10.1016/j.tet.2013.01.072

Catalytic, Enantioselective, and Highly Chemoselective Bromocyclization of Olefinic Dicarbonyl Compounds

Yi Zhao, Xiaojian Jiang and Ying‐Yeung Yeung

Angewandte Chemie, 2013, 125, 8759
DOI: 10.1002/ange.201304107

Enantioselective, Desymmetrizing Bromolactonization of Alkynes

Michael Wilking, Christian Mück-Lichtenfeld, Constantin G. Daniliuc and Ulrich Hennecke

J. Am. Chem. Soc., 2013, 135, 8133
DOI: 10.1021/ja402910d

Regioselective organocatalyzed asymmetric bromolactonization of aryl acrylate-type carboxylic acids: a new approach towards enantioenriched 3-substituted isobenzofuranones

Fabien Gelat, Michaël Coffinet, Stéphane Lebrun, Francine Agbossou-Niedercorn, Christophe Michon and Eric Deniau

Tetrahedron: Asymmetry, 2016, 27, 980
DOI: 10.1016/j.tetasy.2016.07.010

C2-Symmetric Cyclic Selenium-Catalyzed Enantioselective Bromoaminocyclization

Feng Chen, Chong Kiat Tan and Ying-Yeung Yeung

J. Am. Chem. Soc., 2013, 135, 1232
DOI: 10.1021/ja311202e

Bis(μ-iodo)-tetrakis(O-methyl N-phenylthiocarbamate)-tetraiodo-dibismuth

Wafa Arar, Abderrahim Khatyr, Michael Knorr, Carsten Strohmann and Annika Schmidt

Molbank, 2022, 2022, M1381
DOI: 10.3390/M1381

Desymmetrization of Diolefinic Diols by Enantioselective Amino‐thiocarbamate‐Catalyzed Bromoetherification: Synthesis of Chiral Spirocycles

Daniel Weiliang Tay, Gulice Y. C. Leung and Ying‐Yeung Yeung

Angew Chem Int Ed, 2014, 53, 5161
DOI: 10.1002/anie.201310136

Enantioselective Chlorocyclization of Indole Derived Benzamides for the Synthesis of Spiro-indolines

Qin Yin and Shu-Li You

Org. Lett., 2013, 15, 4266
DOI: 10.1021/ol4020943

Catalytic, Enantioselective, and Highly Chemoselective Bromocyclization of Olefinic Dicarbonyl Compounds

Yi Zhao, Xiaojian Jiang and Ying‐Yeung Yeung

Angew Chem Int Ed, 2013, 52, 8597
DOI: 10.1002/anie.201304107

C3‐Symmetric Cinchonine‐Squaramide‐Catalyzed Asymmetric Chlorolactonization of Styrene‐Type Carboxylic Acids with 1,3‐Dichloro‐5,5‐dimethylhydantoin: An Efficient Method to Chiral Isochroman‐1‐ones

Xin Han, Chune Dong and Hai‐Bing Zhou

Adv Synth Catal, 2014, 356, 1275
DOI: 10.1002/adsc.201300915

Carbamate‐Catalyzed Enantioselective Bromolactamization

Yi An Cheng, Wesley Zongrong Yu and Ying‐Yeung Yeung

Angew Chem Int Ed, 2015, 54, 12102
DOI: 10.1002/anie.201504724

Synthesis of Catena-bis(μ-bromo)-(O-methyl-N-phenylthiocarbamate)-dicopper(I) and Its Reactivity towards PAr3 (Ar = Ph, p-Tol)

Wafa Arar, Lydie Viau, Isabelle Jourdain, Michael Knorr, Carsten Strohmann, Rebecca Scheel and Azaiez Ben Akacha

Molbank, 2023, 2023, M1655
DOI: 10.3390/M1655

Cinchona Alkaloids as Organocatalysts in Enantioselective Halofunctionalization of Alkenes and Alkynes

Suqing Zheng, Casi M. Schienebeck, Wei Zhang, Hao‐Yuan Wang and Weiping Tang

Asian J Org Chem, 2014, 3, 366
DOI: 10.1002/ajoc.201400030