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Publications

2024

7) F. Saito 
(((2S,3R)-2,3-Diphenylaziridin-1-yl)imino)-λ4-sulfanone
Encyclopedia of Reagents for Organic Synthesis, 2024.

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6) M. Fimm and F. Saito*

Enantioselective Synthesis of Sulfinamidines via Asymmetric Nitrogen Transfer from N-H Oxaziridines to Sulfenamides 

Angew. Chem. Int. Ed. 2024, 63, e202408380. 

Preprint: 10.26434/chemrxiv-2024-xx8p7

ToC.tiff

5) F. Saito*

Recent Developments on the Synthesis of Sulfoxides via Sulfenate Anions (short review)

Synthesis 2024, 56, 220–228.

Invited contribution (Editor: Prof. Martin Oestreich)

TOCgraphic_short_review.tiff

2023

4) D. Austrup and F. Saito*

A Sulfur Monoxide Surrogate Designed for the Synthesis of Sulfoxides and Sulfinamides

Angew. Chem. Int. Ed. 2023, 62, e202315123.

Preprint: 10.26434/chemrxiv-2023-v613z

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3) F. Saito* and S. Euteneuer

One-Pot, Three-Component Assembly of Sulfides Using a Sulfoxide Reagent as a Sulfur Dication Equivalent

Org. Lett. 2023, 25, 6057–6061.

Highlighted in Organic Chemistry Portal

Preprint: 10.26434/chemrxiv-2023-gh3l0

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2) F. Saito*

A Sulfoxide Reagent for Sulfinylative Cross-Coupling (Synpacts)

Synlett 2023, 34, 1939–1942.

Invited contribution (Editor: Prof. Peter Vollhardt)

2022

1) F. Saito*

A Sulfoxide Reagent for One-Pot, Three-Component Syntheses of Sulfoxides and Sulfinamides

Angew. Chem. Int. Ed. 2022, 61, e202213872.
Preprint: 10.26434/chemrxiv-2022-ql75g

ToC.tiff

Undergraduate, Graduate, and Postdoctoral Studies

k) Roque, J. P. L.; Nunes, C. M.; Saito, F.; Bernhardt, B.; Fausto, R.; Schreiner, P. R. "Competitive heavy-atom tunneling reactions controlled through electronic effects" ChemistryEurope 2024, e202400060.

j) Jiang, T.; Bordi, S.; McMillan, A. E.; Chen, K.-Y.; Saito, F.; Nichols, P. L.; Wanner, B. M.; Bode, J. W. "An integrated console for capsule-based, automated organic synthesis" Chem. Sci. 2021, 12, 6977–6982.

i) Saito, F.; Gerbig, D.; Becker, J.; Schreiner, P. R. “Breaking the symmetry of a meso compound by isotopic substitution: synthesis and stereochemical assignment of monodeuterated cis-perhydroazulene” Org. Lett. 2021, 23, 113–117.

h) Saito, F.; Schreiner, P. R. “Determination of the absolute configurations of chiral alkanes – An analysis of the available tools” Eur. J. Org. Chem. 2020, 6328–6339.

g) Saito, F.; Gerbig, D.; Becker, J.; Schreiner, P. R. “Absolute configuration of trans-perhydroazulene” Org. Lett. 2020, 22, 3895–3899.

f) Saito, F.; Becker, J.; Schreiner, P. R. “Synthesis and conformational analysis of parent perhydroazulenes reveal an energetically preferred cis ring fusion” J. Org. Chem. 2020, 85, 4441–4447.

e) Saito, F.; Trapp, N.; Bode, J. W. "Iterative assembly of polycyclic saturated heterocycles from monomeric building blocks" J. Am. Chem. Soc. 2019, 141, 5544–5554.

d) Saito, F.; Bode, J. W. "Synthesis and stabilities of peptide-based [1]rotaxanes: molecular grafting onto lasso peptide scaffolds" Chem. Sci. 2017, 8, 2878–2884.

c) Saito, F.; Bode, J. W. "Macrocyclic peptides: tying up loose ends" Nat. Chem. 2016, 8, 1085–1086. "News and views" article

b) Saito, F.; Noda, H.; Bode, J. W. "Critical evaluation and rate constants of chemoselective ligation reactions for stoichiometric conjugations in water" ACS Chem. Biol. 2015, 10, 1026–1033.

a) Saito, F.; Aiso, H.; Kochi, T.; Kakiuchi, F. "Palladium-catalyzed regioselective homocoupling of arenes using anodic oxidation: formal electrolysis of aromatic carbon-hydrogen bonds" Organometallics 2014, 33, 6704–6707.

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