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Publications From IIT Hyderabad  

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47. D. Giri, S. Mondal, M. C. Galan*A. Sau*  “Challenges and Opportunities in the Synthesis of Biologically Relevant Flavonoids and Its Glycosides”

Natural Product Reports, 2026, Accepted, xxxxx. DOI

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46. A. Nandy, S. Dey, D. Giri, S, Dwivedi, A. Sau*   “Palladium-Catalyzed Synthesis of S-Glycosides via Stereoretentive Cross-Coupling”

Org.Lett., 2026, 28, 6907-6912

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45. D. Giri, A. Sau*   “Stereocontrolled Glycal Functionalization by Electrochemical

C2-Selenation”

Adv. Synth. Catal., 2026, 368, e70495

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44. S. DwivediA. Sau*  “Direct Synthesis of Glycosyl Fluorides from Hemiacetals Using Diphenylchlorophosphate-KHF₂”

J. Org. Chem., 2026, 91, 6427-6432.

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43. S. Dey, A. Nandy, S. DwivediA. Sau*  “Synthesis of Glycosyl Chlorides and Fluorides via a Mild Chlorination Strategy”

Carbohydrate Research2026, 562, 109841.

(Invited contribution to a special issue on European Carbohydrate Symposium 2025)

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42. I. Paul, S. Dey, J. Sharma, A. Sau* T. K. Panda*   “Zinc-catalyzed Synthesis of β-Keto Trifluoromethyl Sulfone”

J. Org. Chem., 2026, 91, 5434-5438

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41. S. Dwivedi, S. Dey, A. Sau*  “Copper (II)-Mediated Deoxychlorination Synthesis of Glycosyl Chlorides from Glycosyl Hemiacetals”

Chem.Commun2026, 62, 2352-2356.

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2025

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40. S. Dwivedi, S. Paul, A. Sau*  “Diastereoselective Synthesis of N-glycosides via Buchwald-Hartwig Coupling”

Org.Lett2025, 27, 10218-10223.

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39. D. Giri, Raghuvendra, A. Saha, V. S. Manikanta, A. Sau*  “Copper-catalyzed Chemoselective Reduction of α,β-unsaturated Flavone Olefin and It’s Glycosides” Chem.Eur.J2025, 0, e02101.

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38. I. Paul, D. A. Kisan,  S. Dey, A. Sau,* T. K. Panda* “Synthesis of N-Methylated Amines via Reduction of Carbamates Using Amidophosphine borane”

J. Org. Chem., 2025, 90, 10539-10544. 

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37. S. Dey, D. Giri, A. Nandy, A. Sau*  “Supramolecular Assisted O-Acylation of Carbohydrates” 

Green. Chem., 2025, 27, 4995-5000. 

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36. S. Dwivedi,  S. Thakur, A. Sau*  “Thiourea-Catalyzed Glycosylation: A Breakthrough in  Stereoselective Synthesis of Oligosaccharides” 

Chem. Commun.,2025, 61, 4429-4446. 

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35. S. Dey, S. Dwivedi, A. Sau*  “Regioselective O-Arylation of 6-Hydroxy Groups in Carbohydrates” 

Carbohydrate Research.,2025, 552, 109447. 

(Invited contribution to a special issue in honour of Professor Richard R Schmidt)                   

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34. J. Sharma, P. Dutta, A. Sau,* and T. K. Panda*  “Amidophosphine Boranes as Easy Reducing Agents for Efficient Conversion of Nitro Compounds to Primary Amines with Iron Catalyst” 

Applied Organometallic Chemistry, 2025, 39, e70015.

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33. G. S. Kumar, K. Bano, P. Biswal, S. Dey, R. Kumar, A. Sau,*  V. Chandrasekhar* and T. K. Panda*  “Indium-catalyzed hydrosilylation of nitroarenes to aromatic amines”

 Dalton Trans., 2025, 54, 1552-1559.

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32. D. A. Kisan, I. Paul,  S. Dey, A. Sau,* T. K. Panda*  “Facile access to trifluoromethyl propargyl alcohol by metal-free transfer hydrogenation and cyanation of alkynyl Ketone” 

Org. Biomol. Chem., 2025, 23, 197-201.

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2024

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31. S. Dey, S. Dwivedi, D. Giri, A. Sau*  “Benzene-1,3-disulfonyl Fluoride Mediated Synthesis of Glycosyl Fluorides from Glycosyl Hemiacetals” 

Org. Lett., 2024, 26, 10351-10355.

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30. A. Neeliveettil,‡ S. Dey,‡ V. Nomula, S. Thakur, D. Giri, A. Santra, A. Sau* “Deoxyfluorinated Amidation and Esterification of Carboxylic Acid by Pyridinesulfonyl Fluoride” (‡co first author)

Chem.Commun., 2024, 60, 4789 - 4792.

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29. R. K. Meher,  R. Kumar, A. Sau,* T. K. Panda*  “Efficient Hydroboration of Ketones and Imines Using Amidophosphine-borane under Catalyst-Free Conditions” 

Eur. J. Org. Chem., 2024, e202400985.

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28. S. Dwivedi, S. Dey, A. Sau*  “Sugar Functionalized Coumarin Motifs: Synthesis and Applications

Carbohydrate Research., 2024, 544,109244.

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27. D. A. Kisan, I. Paul, A. Sau,* T. K. Panda* Dimethyl Sulfoxide Promoted Quinazolinone Synthesis  
ChemistrySelect., 41,  2024, e202402809.

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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)

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2023

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

Org. Lett., 202325, 7923-7927.

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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.

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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. 

      

 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. 202022, 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

     

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., 201818, 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

      

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.

 

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