In this page, you will find my contributions to the scientific world. The publications were prepared during my prior academic career (MSc to Postdoc). If you are interested in reading any of the article, feel free to reach out to me.
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Iterative Synthesis of Oligosilanes Using Methoxyphenyl- or Hydrogen-Substituted Silylboronates as Building Blocks: A General Synthetic Method for Complex Oligosilanes
Iterative Synthesis of Oligosilanes Using Methoxyphenyl- or Hydrogen-Substituted Silylboronates as Building Blocks: A General Synthetic Method for Complex Oligosilanes
T. Takeuchi, A. Roy, and H. Ito
Silylium-Ion-Initiated Intramolecular Friedel–Crafts-Type Cyclization of 1,1-Difluoroalkenes with Subsequent Hydrodefluorination of C(sp3)–F Bonds
Silylium-Ion-Initiated Intramolecular Friedel–Crafts-Type Cyclization of 1,1-Difluoroalkenes with Subsequent Hydrodefluorination of C(sp3)–F Bonds
A. Roy,‡ H. Gao,‡ H. F. T. Klare, and M. Oestreich
Synthesis of Donor-Stabilized Bis(silylium) Ions and Silylium-Ion-Promoted Organic Transformations
Synthesis of Donor-Stabilized Bis(silylium) Ions and Silylium-Ion-Promoted Organic Transformations
A. Roy, Technische Universität Berlin, 2022. [Dissertation]
Metal-Free Hydrosilylation of Ketenes with Silicon Electrophiles: Access to Fully Substituted Aldehyde-Derived Silyl Enol Ethers
Metal-Free Hydrosilylation of Ketenes with Silicon Electrophiles: Access to Fully Substituted Aldehyde-Derived Silyl Enol Ethers
A. Roy and M. Oestreich
Chem. Eur. J. 2021, 27, 8273–8276.
One of the top downloaded articles during first 12 months of publication
At Long Last: The Me3Si Group as a Masked Alcohol
At Long Last: The Me3Si Group as a Masked Alcohol
A. Roy and M. Oestreich [Highlight]
Synthesis of a Counteranion-Stabilized Bis(silylium) Ion
Synthesis of a Counteranion-Stabilized Bis(silylium) Ion
Q. Wu‡, A. Roy‡, G. Wang, E. Irran, H. F. T. Klare, and M. Oestreich (‡ equal contribution)
Angew. Chem. Int. Ed. 2020, 59, 10523–10526.
Highlighted as a "Very Important Paper (VIP)" by Angewandte Chemie
Silylium-Ion-Promoted Ring-Opening Hydrosilylation and Disilylation of Unactivated Cyclopropanes
Silylium-Ion-Promoted Ring-Opening Hydrosilylation and Disilylation of Unactivated Cyclopropanes
A. Roy, V. Bonetti, G. Wang, Q. Wu, H. F. T. Klare, and M. Oestreich
Catalytic Difunctionalization of Unactivated Alkenes with Unreactive Hexamethyldisilane through Regeneration of Silylium Ions
Catalytic Difunctionalization of Unactivated Alkenes with Unreactive Hexamethyldisilane through Regeneration of Silylium Ions
Q. Wu, A. Roy, E. Irran, Z.-W. Qu, S. Grimme, H. F. T. Klare, and M. Oestreich
Angew. Chem. Int. Ed. 2019, 58, 17307–17311.
Highlighted as a "Very Important Paper (VIP)" by Angewandte Chemie
Highlighted in SYNFACTS 2019, 15, 1427.
C3-Alkenylation between Pyrroles and Aldehydes Mediated by a Brønsted Acid and a Brønsted Base
C3-Alkenylation between Pyrroles and Aldehydes Mediated by a Brønsted Acid and a Brønsted Base
S. Sahu, A. Roy, M. Gorai, S. Guria, and M. S. Maji
Ni(II)-Catalyzed Vinylic C–H Functionalization of 2-Acetamido-3-arylacrylates to Access Isotetronic Acids
Ni(II)-Catalyzed Vinylic C–H Functionalization of 2-Acetamido-3-arylacrylates to Access Isotetronic Acids
B. Roy, E. Das, A. Roy, and D. R. Mal
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