Publications | SauChem

27. A. Neeliveettil,‡ S. Dey,‡ V. Nomula, S. Thakur, D. Giri, A. Santra, A. Sau*, “Deoxyfluorinated Amidation and Esterification of Carboxylic Acid by Pyridinesulfonyl Fluoride” Chem. Commun., 2024, 60, xxxx-xxxx, Accepted.

(‡co first author)

26. S. Dey, S. Thakur, A. Sau* “Glycosyl Fluorides: An Overview of Recent Synthesis and Activation”Trends In Carbohydrate Research., 2024, 16, 118-142. (Invited Article)

25. R. Kumar, R. Meher, J. Sharma, A. Sau,* T. K. Panda* “Amidophosphine Boranes as Hydroboration Reagents for Nitriles, Alkynes, and Carboxylic Acids” Org. Lett., 2023, 25, 7923-7927.

24. G. S. Kumar, R. Kumar, A. Sau, V. Chandrasekhar, T. K. Panda* “Zinc Catalyzed Hydroboration of Esters and Nitriles with Pinacol-borane” J. Org. Chem., 2023, 88, 12613-12622.

PhD & Postdoctoral Publications

23. P. Chatelain, C. Muller, A. Sau, D. Brykczynska; M. Bahadori, C. Rowley, J. Moran “Desulfonative Suzuki-Miyaura Coupling of Sulfonyl Fluorides”

Angew. Chem. Int. Ed., 2021, 60, 25307-25312.

22. A. Sau, K. Nagarajan, B. Patrahau, L. Lethuillier-Karl, R. Vergauwe, A. Thomas, J. Moran, C. Genet, T. W. Ebbesen. “Modifying Woodward-Hoffmann stereoselectivity under vibrational strong coupling”:

Angew. Chem. Int. Ed., 2021, 60, 5712-5717.

(Selected as a Hot paper)

21. C. Palo-Nieto‡, A . Sau‡, R. Jeanneret, P. Payard, M. Martins-Teixeira, I. Carvalho, L. Grimaud, M. C. Galan. “Copper Reactivity can be Tuned to Catalyse the Stereoselective Synthesis of 2-deoxy Glycosides from Glycals”: Org. Lett. 2020, 22, 1991-1996. (‡co first author)

20. I. H. González, E. S.Fernández, A. Sau, C. Nativi, J. G. Fernández, M. C. Galan, C. O. Mellet. “Stereoselective Synthesis of Iminosugar 2-Deoxy(thio)glycosides from Bicyclic Iminoglycal Carbamates Promoted by Cerium(IV) Ammonium Nitrate and Cooperative Brønsted Acid-Type Organocatalysis”

J. Org. Chem., 2020, 85, 5038-5047.

19. M. Ghirardello, H. Ledru, A. Sau, M. C. Galan “Chemo-selective Rh-catalysed Hydrogenation of Azides into Amines”:

Carbohydr. Res., 2020, 489, 107948.

18. P. Chatelain, A. Sau, C. N. Rowley, J. Moran. “Suzuki−Miyaura Coupling of (Hetero)Aryl Sulfones: Complementary Reactivity Enables Iterative Polyaryl Synthesis”:

Angew. Chem. Int. Ed., 2019, 58, 14959-14963.

(Selected as a Hot Paper)

(Featured in Synfacts)

(Top downloaded paper)

17. A. Sau, C. Palo-Nieto, M. C. Galan. “Substrate-controlled direct stereoselective synthesis of deoxyglycosides from glycals using B(C6F5)3 as the Catalyst”:

J. Org. Chem., 2019, 84, 2415–2424.

16. I. Mattsson, M. Lahtinen, A. Peuronen, A. Sau, A. Gunell, T. Saloranta-Simell, R Leino. “Thermal spectroscopic and crystallographic analysis of mannose-derived linear polyols”:

Crystal Growth & Design., 2018, 18, 3151–3160.

15. C. Palo-Nieto, A. Sau, M. C. Galan. “Gold (I) Catalysed Stereoselective Synthesis of Deoxyglycosides”:

J. Am. Chem. Soc., 2017, 139, 14041-14044.

(Featured in Synfacts)

14. C. Palo-Nieto, A. Sau, R. Williams, M. C. Galan. “Cooperative Brønsted Acid-Type Organocatalysis for the Stereoselective Synthesis of Deoxyglycosides”:

J. Org. Chem., 2017, 82, 407-414.

13. A. Sau, M. C. Galan. “Palladium-Catalyzed α-Stereoselective O-Glycosylation of O(3)-Acylated Glycals”:

Org. Lett., 2017, 19, 2857-2860.

12. A. Sau, R. Williams, C. Palo-Nieto, A. Franconetti, S. Medina, M. C. Galan. “Palladium-Catalysed Direct Stereoselective Synthesis of Deoxyglycosides from Glycals”:

Angew. Chem. Int. Ed., 2017, 56, 3640-3644.

11. P. K. Parida‡, A. Sau‡, T. Ghosh, K. Jana, K. Biswas, S. Raha and A. K. Misra, “Synthesis and evaluation of triazole linked glycosylated 18b-glycyrrhetinic acid derivatives as anticancer agents”:

Bioorg. Med. Chem. Lett., 2014, 24, 3865-3868. (‡ co first author)

10. M. Jana‡, A. Sau‡, A. K. Misra, “Synthesis of a pentasaccharide repeating unit of the O-antigen of enteroadherent Escherichia coli O154 strain”.

Tetrahedron: Asymmetry, 2014, 25, 632-636. (‡ co first author)

9. A. Sau, D. Dhara, A. K. Misra. “Concise synthesis of a pentasaccharide repeating unit corresponding to the O-antigen of Escherichia coli O102”:

Tetrahedron: Asymmetry, 2013, 24, 942-946.

8. A. Sau, A. K. Misra. “Convergent synthesis of the tetrasaccharide repeating unit of the cell wall lipopolysaccharide of Escherichia coli O40”:

Beilstein. J. Org. Chem, 2012, 8, 2053-2059.

7. A. Sau, A. Santra, A. K. Misra. “Stereoselective glycosylations by nitrosyl tetrafluoroborate catalyzed activation of glycosyl trichloroacetimidate derivatives”:

Synlett, 2012, 2341-2348.

6. A. Sau, A. K. Misra. “Reaction of glycal derivatives with alcohols in the presence of N-bromosuccinimide and diphenyldiselenide”: preparation of 2-deoxy-2-phenylselenyl glycosides:

Carbohydr. Res., 2012, 361, 41-48.

5. A. Sau, R. Panchadhayee, D. Ghosh, A. K. Misra. “Synthesis of a tetrasaccharide analog corresponding to the repeating unit of the O-polysaccharide of Salmonella enterica O59”: Unexpected stereo outcome in glycosylation:

Carbohydr. Res., 2012, 352, 18-22

4. A. Sau, A. K. Misra. “Synthesis of the tetrasaccharide motif and its structural analog corresponding to the O-specific lipopolysaccharide of Escherichia coli O75”:

PLoS One, 2012, 7(5) e37291.

3. A. Sau, A. K. Misra. “Oderless eco-friendly synthesis of thio- and selenoglycosides in ionic liquid”:

Synlett, 2011, 1905-1911.

2. A. Sau, A. K. Misra. “Environmentally Benign Preparation of Benzylidene Acetal of Carbohydrate Derivatives in PEG-600”:

J. Carbohydr. Chem, 2011, 30, 41-46.

1. A. Santra, A. Sau, A. K. Misra. “Synthesis of thioglycosides in room temperature Ionic Liquid”:

J. Carbohydr. Chem., 2011, 30, 85-93.