15. Das, A.,* Teichert, J. F.* Eliminations to Form Alkenes, Allenes, Alkynes and Related Reactions. In Comprehensive Organic Synthesis, 3rd edition; Molander, G., Knochel, P., Eds., Elsevier, 2025, vol. 7, pp. 388–418. DOI: 10.1016/B978-0-323-96025-0.00012-0. www.sciencedirect.com/science/chapter/referencework/abs/pii/B9780323960250000120?via%3Dihub  (Book Chapter)

14. Das, A.,* Panda, T.* Metal-Free Catalytic Hydroboration of Unsaturated Compounds: A Greener Strategy for the Synthesis of Organoboranes. ChemCatChem 2023, 15, e202201011. chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/cctc.202201011

13. Ishitani, H.*; Kawase, T.; Das, A., Kobayashi, S.* Catalytic hydrogenative dechlorination reaction for efficient synthesis of a key intermediate of SDHI fungicides under continuous-flow conditions. Catal. Sci. Technol. 2023, 13, 3282–3291. pubs.rsc.org/en/content/articlelanding/2023/cy/d3cy00182b 

12. Das, A., Chatani, N.* Rh(I)-Catalysed Imine-Directed C−H Functionalization by the Oxidative [3+2] Cycloaddition of Benzylamine Derivatives with Maleimides. Chem. Commun. 2022, 58, 1123–1126. pubs.rsc.org/en/content/articlelanding/2022/cc/d1cc06622f

11. Das, A.,* Rej, S.,* Panda, T.* Aluminium Complexes: Next-Generation Catalysts in Selective Hydroboration. Dalton Trans. 2022, 51, 3027–3040. pubs.rsc.org/en/content/articlelanding/2022/dt/d1dt03703j  

10. Das, A., Chatani, N.* Rh(II)-Catalyzed C–H Alkylation of Benzylamines with Unactivated Alkenes: The Influence of Acid on Linear and Branch Selectivity. Org. Lett. 2021, 23, 4273–4278. pubs.acs.org/doi/10.1021/acs.orglett.1c01224 

9. Das, A., Chatani, N.* Rh(I)- and Rh(II)-Catalyzed C–H Alkylation of Benzylamines with Alkenes and Its Application in Flow Chemistry. Chem. Sci. 2021, 12, 3202–3209. (Highlighted in SYNFACTS 2021, 17(03), 0358) pubs.rsc.org/en/content/articlelanding/2021/sc/d0sc05813k 

8. 6. Das, A., Chatani, N.* The Directing Group: A Tool for Efficient and Selective C−F Bond Activation. ACS Catal. 2021, 11, 12915−12930. pubs.acs.org/doi/10.1021/acscatal.1c03896 

7. Rej, S.,* Das, A.,* Panda, T.* Overview of Regioselective and Stereoselective Catalytic Hydroboration of Alkynes. Adv. Synth. Catal. 2021, 363, 4818–4840. advanced.onlinelibrary.wiley.com/doi/10.1002/adsc.202100950 

6. Rej, S., Das, A., Chatani, N.* Pyrimidine-Directed Metal-Free C‒H Borylation of 2‐Pyrimidylanilines: A Useful Process for Tetra-Coordinated Triarylborane Synthesis. Chem. Sci. 2021, 12, 11447–11454. pubs.rsc.org/en/content/articlelanding/2021/sc/d1sc02937a 

5. Ohara, N., Das, A., Mahato, S. K., Chatani, N.* Synthesis of α-Amino Acid Derivatives through the Iridium-Catalyzed α-C-H Amidation of 2-Acylimidazoles with Dioxazolones under Continuous-Flow. Chem. Lett. 2021, 50, 1722–1724. academic.oup.com/chemlett/article/50/9/1722/7371871 

4. Rej, S., Das, A., Chatani, N.* Strategic Evolution in Transition Metal-Catalyzed Directed C–H Bond Activation and Future Directions. Coord. Chem. Rev. 2021, 431, 213683–213719. www.sciencedirect.com/science/article/pii/S0010854520307906 

3. Das, A., Ishitani, H., Kobayashi, S.* Toward Continuous-Flow Synthesis of Biologically Interesting Pyrazole Derivatives. Adv. Synth. Catal. 2019, 361, 5127–5132. advanced.onlinelibrary.wiley.com/doi/full/10.1002/adsc.201900954 

2. Das, A., Watanabe, K.*, Morimoto, H., Ohshima, T.* Boronic Acid Accelerated Three-Component Reaction for the Synthesis of a-Sulfanyl-Substituted Indole-3-acetic Acids. Org. Lett. 2017, 19, 5794–5797. pubs.acs.org/doi/10.1021/acs.orglett.7b02727 

1. Das, A., Reddy, A.G.K., Krishna, J., Satyanarayana, G.* An Efficient Synthesis of Highly Substituted Indanones and Chalcones Promoted by Superacid. RSC Adv. 2014, 4, 26662–26666. pubs.rsc.org/en/content/articlelanding/2014/ra/c4ra04763j