Citations to this article as recorded by CrossRef and RSC Journals (35 citations).

Synthesis and biological evaluation of moiramide B derivatives

Oliver Andler and Uli Kazmaier

Org. Biomol. Chem., 2024, 22, 5284
DOI: 10.1039/D4OB00856A

Electrochemical collective synthesis of labeled pyrroloindoline alkaloids with Freon-type methanes as functional C1 synthons

Chao Chen, Ru-Xin Liu, Feng Xiong, Zi-Hao Li, Jun-Chen Kang, Tong-Mei Ding and Shu-Yu Zhang

Chem. Commun., 2022, 58, 9230
DOI: 10.1039/D2CC03301A

Syntheses of bottromycin derivatives via Ugi-reactions and Matteson homologations

Etienne Bickel and Uli Kazmaier

Org. Biomol. Chem., 2024, 22, 8811
DOI: 10.1039/D4OB01373E

Synthesis of oxylipids via a boronic ester cycloetherification approach

Markus Tost and Uli Kazmaier

Org. Chem. Front., 2025, 12, 3288
DOI: 10.1039/D5QO00213C

Total synthesis and biological evaluation of histone deacetylase inhibitor WF-3161

Michael Kohr, Niklas Papenkordt, Manfred Jung and Uli Kazmaier

Org. Biomol. Chem., 2023, 21, 4382
DOI: 10.1039/D3OB00641G

B(MIDA)-directed site-selective intermolecular halofluoroalkylation of alkenes: synthesis of diversely functionalized building blocks

Hengbo Wu, Ruitong Luo, Jingjing Peng, Zijian Han, Renjie Zhang, Zhijian Xu, Weiliang Zhu, Hong Liu and Chunpu Li

Chem. Sci., 2025, 16, 2710
DOI: 10.1039/D4SC07900K

Stereoselective synthesis of five- and six-membered carbocycles via Matteson homologation/ring closing metathesis

Thorsten Kinsinger and Uli Kazmaier

Org. Chem. Front., 2023, 10, 2963
DOI: 10.1039/D3QO00457K

Matteson Homologation-Based Total Synthesis of Meliponamycin A

Oliver Andler and Uli Kazmaier

Org. Lett., 2024, 26, 148
DOI: 10.1021/acs.orglett.3c03766

1,2‐Boronate Rearrangement: An Efficient Tool for the Opening, Functionalization and Formation of Strained Cycles

Rémi Blieck and Aurélien de la Torre

Eur J Org Chem, 2022, 2022
DOI: 10.1002/ejoc.202200920

Catalytic Amide Activation with Thermally Stable Molybdenum(VI) Dioxide Complexes

Garrett E. Evenson, Wyatt C. Powell, Aaron B. Hinds and Maciej A. Walczak

J. Org. Chem., 2023, 88, 6192
DOI: 10.1021/acs.joc.3c00218

Stereoselective Synthesis of a Protected Side Chain of Meliponamycin A

Oliver Andler and Uli Kazmaier

Org. Lett., 2022, 24, 2541
DOI: 10.1021/acs.orglett.2c00701

Synthesis and late stage modifications of Cyl derivatives

Phil Servatius and Uli Kazmaier

Beilstein J. Org. Chem., 2022, 18, 174
DOI: 10.3762/bjoc.18.19

A Matteson Homologation‐Based Synthesis of Doliculide and Derivatives

Markus Tost, Oliver Andler and Uli Kazmaier

Eur J Org Chem, 2021, 2021, 6459
DOI: 10.1002/ejoc.202101345

Natural Cyclic Peptides: Synthetic Strategies and Biomedical Applications

Devan Buchanan, Shogo Mori, Ahmed Chadli and Siva S. Panda

Biomedicines, 2025, 13, 240
DOI: 10.3390/biomedicines13010240

Syntheses of Marine Natural Products via Matteson Homologations and Related Processes

Uli Kazmaier

Marine Drugs, 2025, 23, 20
DOI: 10.3390/md23010020

Synthesis of HC-Toxin via Matteson Homologation and C–H Functionalization

Michael Kohr and Uli Kazmaier

J. Org. Chem., 2023, 88, 10869
DOI: 10.1021/acs.joc.3c00914

Stereoselective Synthesis of α‐Azido Esters and α‐Amino Acid Derivatives via Matteson Homologation of Boronic Esters

Alexander Horn, Emanuel Papadopoulos, Thorsten Kinsinger, Jennifer Greve, Etienne Bickel, Stavroula Pachoula and Uli Kazmaier

Zeitschrift anorg allge chemie, 2024, 650
DOI: 10.1002/zaac.202400113

Total Synthesis of Moiramide B Using an Allylic Alkylation Approach

Cynthia Prudel and Uli Kazmaier

Synlett, 2024, 35, 2133
DOI: 10.1055/s-0042-1751578

Application of Allylzinc Reagents as Nucleophiles in Matteson Homologations

Oliver Andler and Uli Kazmaier

Org. Lett., 2021, 23, 8439
DOI: 10.1021/acs.orglett.1c03164

Total Synthesis of Thiamyxins A–C and Thiamyxin E, a Potent Class of RNA‐Virus‐Inhibiting (Cyclo)depsipeptides

Kevin Bauer and Uli Kazmaier

Angew Chem Int Ed, 2023, 62
DOI: 10.1002/anie.202305445

Total Synthesis of Salviachinensine A Using a Matteson Homologation Approach

Merlin Kempf, Oliver Andler and Uli Kazmaier

Helvetica Chimica Acta, 2023, 106
DOI: 10.1002/hlca.202300136

Stereoselective Syntheses of Highly Substituted Tetrahydrofurans based on Matteson Homologations

Markus Tost and Uli Kazmaier

Chemistry A European J, 2025, 31
DOI: 10.1002/chem.202500560

Totalsynthese von Thiamyxin A–C und Thiamyxin E, potente RNA‐Virus inhibierende (Cyclo)depsipeptide

Kevin Bauer and Uli Kazmaier

Angewandte Chemie, 2023, 135
DOI: 10.1002/ange.202305445

Stereoselective Synthesis of a Protected Side Chain of Callipeltin A

Alexander Horn and Uli Kazmaier

Org. Lett., 2022, 24, 7072
DOI: 10.1021/acs.orglett.2c02586

Combining Matteson Homologations and Claisen Rearrangements – An Efficient Protocol for Amino Acid Synthesis

Thorsten Kinsinger and Uli Kazmaier

Eur J Org Chem, 2023, 26
DOI: 10.1002/ejoc.202201345

Isomerization-Free Matteson Homologations of Substituted Allylboronic Esters

Thorsten Kinsinger, Ronja Priester and Uli Kazmaier

Org. Lett., 2023, 25, 5902
DOI: 10.1021/acs.orglett.3c02199

A Straightforward Synthesis of Emericellamide A Using Matteson’s Homologation Approach

Ronja Priester and Uli Kazmaier

Synlett, 2023, 34, 2159
DOI: 10.1055/a-2077-2113

Iterative Catalyst-Controlled Diastereoselective Matteson Homologations Enable the Selective Synthesis of Benzestrol Isomers

Samantha R. Angle, Hayden A. Sharma, Christie K. Choi, Kathryn E. Carlson, Yingwei Hou, Jerome C. Nwachukwu, Sung Hoon Kim, Benita S. Katzenellenbogen, Kendall W. Nettles, John A. Katzenellenbogen and Eric N. Jacobsen

J. Am. Chem. Soc., 2024, 146, 30771
DOI: 10.1021/jacs.4c12857

Catalysis Driven Six-Step Synthesis of Apratoxin A Key Polyketide Fragment

Na Shao, Jean Rodriguez and Adrien Quintard

Org. Lett., 2022, 24, 6537
DOI: 10.1021/acs.orglett.2c02482

Depsipeptides Targeting Tumor Cells: Milestones from In Vitro to Clinical Trials

Plinio A. Trinidad-Calderón, Carlos Daniel Varela-Chinchilla and Silverio García-Lara

Molecules, 2023, 28, 670
DOI: 10.3390/molecules28020670

Synthesis and Late-Stage Modification of (−)-Doliculide Derivatives Using Matteson’s Homologation Approach

Markus Tost and Uli Kazmaier

Marine Drugs, 2024, 22, 165
DOI: 10.3390/md22040165

Stereoselective Synthesis of Secondary and Tertiary Boronic Esters via Matteson Homologation

Markus Tost and Uli Kazmaier

Org. Lett., 2023, 25, 6835
DOI: 10.1021/acs.orglett.3c02360

Stereoselective Synthesis of Highly Substituted O-Heterocycles via Matteson Homologation: A Ring-Closing Metathesis Approach

Thorsten Kinsinger, Patrick Schäfer and Uli Kazmaier

Org. Lett., 2023, 25, 3303
DOI: 10.1021/acs.orglett.3c01099

Matteson Homologation of Arylboronic Esters

Thorsten Kinsinger and Uli Kazmaier

Eur J Org Chem, 2022, 2022
DOI: 10.1002/ejoc.202200625

Application of Vinyl Nucleophiles in Matteson Homologations

Thorsten Kinsinger and Uli Kazmaier

Org. Lett., 2022, 24, 3599
DOI: 10.1021/acs.orglett.2c01119