Cross Reference Logo
Citations to this article as recorded by CrossRef and RSC Journals (53 citations).

Inexpensive multigram-scale synthesis of cyclic enamines and 3-N spirocyclopropyl systems
Pratik Kumar, Omar Zainul and Scott T. Laughlin
Org. Biomol. Chem., 2018, 16, 652
DOI: 10.1039/C7OB02659E

Construction of heterocyclic rings from cyclopropenes
Hengrui Huo and Yuefa Gong
Org. Biomol. Chem., 2022, 20, 3847
DOI: 10.1039/D1OB02450G

Recent developments in cyclopropene chemistry
Penghua Li, Xiaoyu Zhang and Min Shi
Chem. Commun., 2020, 56, 5457
DOI: 10.1039/D0CC01612H

Fast, irreversible modification of cysteines through strain releasing conjugate additions of cyclopropenyl ketones
Natalee J. Smith, Katarina Rohlfing, Lisa A. Sawicki, Prathamesh M. Kharkar, Samantha J. Boyd, April M. Kloxin and Joseph M. Fox
Org. Biomol. Chem., 2018, 16, 2164
DOI: 10.1039/C8OB00166A

Mechanisms and Substituent Effects of Metal-Free Bioorthogonal Reactions
Titas Deb, Julian Tu and Raphael M. Franzini
Chem. Rev., 2021, 121, 6850
DOI: 10.1021/acs.chemrev.0c01013

C–C Bond Cleavages of Cyclopropenes: Operating for Selective Ring-Opening Reactions
Rubén Vicente
Chem. Rev., 2021, 121, 162
DOI: 10.1021/acs.chemrev.0c00151

Engineering protein prenylation: an emerging tool for selective protein modification
Sneha Venkatachalapathy, Caitlin Lichtenfels, Carston R. Wagner and Mark D. Distefano
Biochemical Society Transactions, 2025, 53, 1129
DOI: 10.1042/BST20253076

Catalytic Enantioselective Cyclopropenation of Internal Alkynes: Access to Difluoromethylated Three‐Membered Carbocycles
Zhi‐Qi Zhang, Meng‐Meng Zheng, Xiao‐Song Xue, Ilan Marek, Fa‐Guang Zhang and Jun‐An Ma
Angew Chem Int Ed, 2019, 58, 18191
DOI: 10.1002/anie.201911701

Carbene-Stabilized Aluminacyclopropene–Cyclopropenylalane Rearrangement
Xin Zhang, Hongyu Wang, Lingbing Kong and Liu Leo Liu
Organometallics, 2024, 43, 2392
DOI: 10.1021/acs.organomet.4c00147

Concise Synthesis of Functionalized Cyclobutene Analogues for Bioorthogonal Tetrazine Ligation
Jiayu Sun, Jie Li, Hongbao Sun, Chunling Li and Haoxing Wu
Molecules, 2021, 26, 276
DOI: 10.3390/molecules26020276

Lipidated cyclopropenes via a stable 3-N spirocyclopropene scaffold
Pratik Kumar, Ting Jiang, Omar Zainul, Alyssa N. Preston, Sining Li, Joshua D. Farr, Pavit Suri and Scott T. Laughlin
Tetrahedron Letters, 2018, 59, 3435
DOI: 10.1016/j.tetlet.2018.08.010

Synthesis of Functionalized α‐Vinyl Aldehydes from Enaminones
Jie Chen, Pan Guo, Jianguo Zhang, Jiaxin Rong, Wangbin Sun, Yaojia Jiang and Teck‐Peng Loh
Angewandte Chemie, 2019, 131, 12804
DOI: 10.1002/ange.201906213

Visible-Light-Mediated Addition of Phenacyl Bromides onto Cyclopropenes
Nitin S. Dange, Ashique Hussain Jatoi, Frédéric Robert and Yannick Landais
Org. Lett., 2017, 19, 3652
DOI: 10.1021/acs.orglett.7b01651

Synthetic Applications of Cyclopropene and Cyclopropenone: Recent Progress and Developments
Bishnu Prasad Raiguru, Sabita Nayak, Deepak Ranjan Mishra, Tapaswini Das, Seetaram Mohapatra and Nilima Priyadarsini Mishra
Asian J Org Chem, 2020, 9, 1088
DOI: 10.1002/ajoc.202000193

Hyperconjugative Antiaromaticity Activates 4H-Pyrazoles as Inverse-Electron-Demand Diels–Alder Dienes
Brian J. Levandowski, Nile S. Abularrage, K. N. Houk and Ronald T. Raines
Org. Lett., 2019, 21, 8492
DOI: 10.1021/acs.orglett.9b03351

Modular Enzyme‐ and Light‐Based Activation of Cyclopropene–Tetrazine Ligation
Ting Jiang, Pratik Kumar, Wei Huang, Wei‐Siang Kao, Adrian O. Thompson, Frank M. Camarda and Scott T. Laughlin
ChemBioChem, 2019, 20, 2222
DOI: 10.1002/cbic.201900137

Photo-cycloaddition reactions of vinyldiazo compounds
Ming Bao, Klaudia Łuczak, Wojciech Chaładaj, Marriah Baird, Dorota Gryko and Michael P. Doyle
Nat Commun, 2024, 15
DOI: 10.1038/s41467-024-48274-5

Comparative Study of Click Handle Stability in Common Ligation Conditions
Caitlin Fawcett, Joe Watson, Stephen Richards, Alfred E. Doherty, Hikaru Seki, Elizabeth A. Love, Charlotte H. Coles, Diane M. Coe and Craig Jamieson
Bioconjugate Chem., 2025, 36, 1054
DOI: 10.1021/acs.bioconjchem.5c00095

Rapid and Efficient Generation of Stable Antibody–Drug Conjugates via an Encoded Cyclopropene and an Inverse‐Electron‐Demand Diels–Alder Reaction
Benjamí Oller‐Salvia, Gene Kym and Jason W. Chin
Angewandte Chemie, 2018, 130, 2881
DOI: 10.1002/ange.201712370

Constructing New Bioorthogonal Reagents and Reactions
R. David Row and Jennifer A. Prescher
Acc. Chem. Res., 2018, 51, 1073
DOI: 10.1021/acs.accounts.7b00606

Three-Membered Aluminacycles
Chenting Yan and Rei Kinjo
J. Am. Chem. Soc., 2023, 145, 12967
DOI: 10.1021/jacs.3c03152

In Vivo Applications of Bioorthogonal Reactions: Chemistry and Targeting Mechanisms
Madonna M. A. Mitry, Francesca Greco and Helen M. I. Osborn
Chemistry A European J, 2023, 29
DOI: 10.1002/chem.202203942

Cyclopropenes as Chemical Reporters for Dual Bioorthogonal and Orthogonal Metabolic Labeling of DNA
Nicola Seul, Dennis Lamade, Petko Stoychev, Michaela Mijic, Rita T. Michenfelder, Lisa Rieger, Philipp Geng and Hans‐Achim Wagenknecht
Angew Chem Int Ed, 2024, 63
DOI: 10.1002/anie.202403044

Efficient Synthesis of Arylated Furans by a Sequential Rh‐Catalyzed Arylation and Cycloisomerization of Cyclopropenes
Xiaoming Wang, Andreas Lerchen, Constantin G. Daniliuc and Frank Glorius
Angew Chem Int Ed, 2018, 57, 1712
DOI: 10.1002/anie.201712019

Catalytic Synthesis of Trifluoromethyl Cyclopropenes and Oligo‐Cyclopropenes
Uyen P. N. Tran, Renè Hommelsheim, Zhen Yang, Claire Empel, Katharina J. Hock, Thanh V. Nguyen and René M. Koenigs
Chemistry A European J, 2020, 26, 1254
DOI: 10.1002/chem.201904680

Caged Cyclopropenes with Improved Tetrazine Ligation Kinetics
Pratik Kumar, Omar Zainul, Frank M. Camarda, Ting Jiang, John A. Mannone, Wei Huang and Scott T. Laughlin
Org. Lett., 2019, 21, 3721
DOI: 10.1021/acs.orglett.9b01177

A Cyclopropene Electrophile that Targets Glutathione S‐Transferase Omega‐1 in Cells
Gustav J. Wørmer, Bente K. Hansen, Johan Palmfeldt and Thomas B. Poulsen
Angewandte Chemie, 2019, 131, 12044
DOI: 10.1002/ange.201907520

Cycloprop-2-ene-1-carboxylates: Potential chemical biology tools in the early growth stage of Arabidopsis thaliana
Tomoyuki Koyama, Ikuo Takahashi and Tadao Asami
J. Pestic. Sci., 2023, 48, 61
DOI: 10.1584/jpestics.D22-034

Trifunctional Saxitoxin Conjugates for Covalent Labeling of Voltage‐Gated Sodium Channels**
Darren S. Finkelstein and J. Du Bois
ChemBioChem, 2023, 24
DOI: 10.1002/cbic.202300493

Synergistic Dual Directing Groups-Enabled Diastereoselective C–H Cyclopropylation via Rh(III)-Catalyzed Couplings with Cyclopropenyl Alcohols
Min Wu, Shuang Lin, Guoxun Zhu, Ming Sun, Zhi Zhou, Hui Gao and Wei Yi
Org. Lett., 2020, 22, 1295
DOI: 10.1021/acs.orglett.9b04608

Synthesis of Functionalized α‐Vinyl Aldehydes from Enaminones
Jie Chen, Pan Guo, Jianguo Zhang, Jiaxin Rong, Wangbin Sun, Yaojia Jiang and Teck‐Peng Loh
Angew Chem Int Ed, 2019, 58, 12674
DOI: 10.1002/anie.201906213

Bioorthogonal chemistry: Optimization and application updates during 2013–2017
Li-Huai Qin, Wei Hu and Ya-Qiu Long
Tetrahedron Letters, 2018, 59, 2214
DOI: 10.1016/j.tetlet.2018.04.058

Cycloaddition of Strained Cyclic Alkenes and Ortho-Quinones: A Distortion/Interaction Analysis
Jorge Escorihuela, Wilhelmus J. E. Looijen, Xiao Wang, Adelia J. A. Aquino, Hans Lischka and Han Zuilhof
J. Org. Chem., 2020, 85, 13557
DOI: 10.1021/acs.joc.0c01674

Bioorthogonal Ligations and Cleavages in Chemical Biology
Youshan Li and Hua Fu
ChemistryOpen, 2020, 9, 835
DOI: 10.1002/open.202000128

Rh-catalyzed double carbonylation of cyclopropenes toward valerolactone derivatives via cleavage of carbon–carbon double bonds
Song-Zhou Cai, Can Li, Suliang Wang, Rongrong Yu, Juntao Ye and Xianjie Fang
Sci. China Chem., 2025, 68, 3667
DOI: 10.1007/s11426-024-2535-y

Stable cyclopropene-containing analogs of the amino acid neurotransmitter glutamate
Pratik Kumar, Wei Huang, David Shukhman, Frank M. Camarda and Scott T. Laughlin
Tetrahedron Letters, 2019, 60, 1476
DOI: 10.1016/j.tetlet.2019.04.046

Specificity of internal rotation in aldehydes with three-membered rings
Vadim A. Bataev and Sergey S. Styopin
Mendeleev Communications, 2023, 33, 416
DOI: 10.1016/j.mencom.2023.04.037

Developing bioorthogonal probes to span a spectrum of reactivities
Sean S. Nguyen and Jennifer A. Prescher
Nat Rev Chem, 2020, 4, 476
DOI: 10.1038/s41570-020-0205-0

Photochemical Disulfide–Ene Modification Enhances Protein Sequencing and Disulfide Mapping by Mass Spectrometry
Xiaoyue Yang, Longfei Zhang and Yu Xia
Anal. Chem., 2021, 93, 15231
DOI: 10.1021/acs.analchem.1c04214

Exosomes as Novel Delivery Systems for Application in Traditional Chinese Medicine
Qi Chen, Di Wu, Yi Wang and Zhong Chen
Molecules, 2022, 27, 7789
DOI: 10.3390/molecules27227789

Trans-[bis(benzimidazol-2-ylidene)dichlorido]platinum(II) complexes with peculiar modes of action and activity against cisplatin-resistant cancer cells
Sofia I. Bär, Sebastian W. Schleser, Natalie Oberhuber, Alexander Herrmann, Luca Schlotte, Stefanie E. Weber and Rainer Schobert
Journal of Inorganic Biochemistry, 2023, 238, 112028
DOI: 10.1016/j.jinorgbio.2022.112028

Broadening the Utility of Farnesyltransferase-Catalyzed Protein Labeling Using Norbornene–Tetrazine Click Chemistry
Shelby A. Auger, Sneha Venkatachalapathy, Kiall Francis G. Suazo, Yiao Wang, Alexander W. Sarkis, Kaitlyn Bernhagen, Katarzyna Justyna, Jonas V. Schaefer, James W. Wollack, Andreas Plückthun, Ling Li and Mark D. Distefano
Bioconjugate Chem., 2024, 35, 922
DOI: 10.1021/acs.bioconjchem.4c00072

Rapid and Efficient Generation of Stable Antibody–Drug Conjugates via an Encoded Cyclopropene and an Inverse‐Electron‐Demand Diels–Alder Reaction
Benjamí Oller‐Salvia, Gene Kym and Jason W. Chin
Angew Chem Int Ed, 2018, 57, 2831
DOI: 10.1002/anie.201712370

Mutually Orthogonal Bioorthogonal Reactions: Selective Chemistries for Labeling Multiple Biomolecules Simultaneously
Kevin R. Venrooij, Lucienne de Bondt and Kimberly M. Bonger
Top Curr Chem (Z), 2024, 382
DOI: 10.1007/s41061-024-00467-8

Physicochemical Characterization of Crithmum maritimum L. and Daucus carota subsp. gummifer (Syme) Hook.fil. and Their Antimicrobial Activity against Apple Tree and Grapevine Phytopathogens
Eva Sánchez-Hernández, Laura Buzón-Durán, Celia Andrés-Juan, Belén Lorenzo-Vidal, Jesús Martín-Gil and Pablo Martín-Ramos
Agronomy, 2021, 11, 886
DOI: 10.3390/agronomy11050886

Cu(I)-Catalyzed Intramolecular Tandem Cyclization of N-Indole-Tethered Cyclopropenes: Synthesis of Functionalized Hydrogenated Diazabenzo[a]cyclopenta[cd]azulene Derivatives
Peng-Hua Li, Song Yang, Tong-Gang Hao, Qin Xu and Min Shi
Org. Lett., 2019, 21, 3162
DOI: 10.1021/acs.orglett.9b00864

Ultrasonic Preparation and Reactivity of 4,5-dihydro-1H-pyrazole Derivatives
Ahlem Guesmi and Naoufel Ben Hamadi
LOC, 2022, 19, 429
DOI: 10.2174/1570178617666210108113916

Recent Advances in the Transformation of Difluorocyclopropenes★
Huang Jiapian, Liu Fei and Wu Jie
Acta Chimica Sinica, 2023, 81, 520
DOI: 10.6023/A23030088

Catalytic Enantioselective Cyclopropenation of Internal Alkynes: Access to Difluoromethylated Three‐Membered Carbocycles
Zhi‐Qi Zhang, Meng‐Meng Zheng, Xiao‐Song Xue, Ilan Marek, Fa‐Guang Zhang and Jun‐An Ma
Angewandte Chemie, 2019, 131, 18359
DOI: 10.1002/ange.201911701

Effiziente Synthese von arylierten Furanen durch sequentielle Rhodium‐katalysierte Arylierung und Cycloisomerisierung von Cyclopropenen
Xiaoming Wang, Andreas Lerchen, Constantin G. Daniliuc and Frank Glorius
Angewandte Chemie, 2018, 130, 1728
DOI: 10.1002/ange.201712019

Isolable Copper(I) η2-Cyclopropene Complexes
Anurag Noonikara-Poyil, Shawn G. Ridlen and H. V. Rasika Dias
Inorg. Chem., 2020, 59, 17860
DOI: 10.1021/acs.inorgchem.0c02886

A Cyclopropene Electrophile that Targets Glutathione S‐Transferase Omega‐1 in Cells
Gustav J. Wørmer, Bente K. Hansen, Johan Palmfeldt and Thomas B. Poulsen
Angew Chem Int Ed, 2019, 58, 11918
DOI: 10.1002/anie.201907520

Cyclopropene als Chemische Reporter für die Duale Bioorthogonale und Orthogonale Metabolische Markierung von DNA
Nicola Seul, Dennis Lamade, Petko Stoychev, Michaela Mijic, Rita T. Michenfelder, Lisa Rieger, Philipp Geng and Hans‐Achim Wagenknecht
Angewandte Chemie, 2024, 136
DOI: 10.1002/ange.202403044