Mukherjee, A.,^‡ Sanz-Matias, A.,^‡ Velpula, G., Waghray, D., Ivasenko, O., Bilbao, N., Harvey, J. *, Mali, K. *, De Feyter, S. *,

Chem. Sci., 2019, 10, 3881-389. (^‡Equal contribution)

18. Cocrystal formation by ionic liquid-assisted grinding: Case study with cocrystals of caffeine

Mukherjee, A., Rogers, R. D. and Myerson, A. S.*

CrystEngComm, 2018, 20, 3817-21.

17. Exploring the role of ionic liquids to tune the polymorphic outcome of organic compounds,

Zeng, Q.,^‡ Mukherjee, A.,^‡ Muller, P., Rogers, R. D.  and Myerson, A. S.*

Chem. Sci., 2018, 9, 1510-20. (^‡Equal contribution)

16. Two-Dimensional Crystal Engineering using Halogen and Hydrogen Bonds: Towards Structural Landscapes,

Mukherjee, A., Teyssandier, J., Hennrich, G., De Feyter, S.*, Mali, K. S*

Chem. Sci., 2017, 8, 3759-69.

15. Crystal chemistry and photomechanical behavior of 3, 4-dimethoxycinnamic acid: correlation between maximum yield in the solid-state topochemical reaction and cooperative molecular motion

Mishra, M.K., Mukherjee, A., Ramamurty, U.,* Desiraju, G. R.*,

IUCrJ, 2015, 2, 653-60.

14. Building upon supramolecular synthons: Some aspects of crystal engineering

Mukherjee, A.*

Cryst. Growth Des., 2015, 15, 3076-85.

2011-2014

13. Aniline-phenol recognition: From solution through supramolecular synthons to cocrystals

Mukherjee, A., Dixit, K., Sarma, S. P., Desiraju, G. R.*

 IUCrJ, 2014, 1, 228-39.

12. Combinatorial exploration of structural landscape of acid-pyridine cocrystals,

Mukherjee, A., Desiraju G. R.*

Cryst. Growth Des., 2014, 14, 1375-85.

11. Halogen bonds in crystal engineering: Like hydrogen bonds yet different,

Mukherjee, A.; Tothadi, S.; Desiraju, G. R.*

Acc. Chem. Res., 2014, 47, 2514-24.

10. Halogen bonds in some dihalogenated phenols: applications to crystal engineering

Mukherjee, A., Desiraju, G. R.

IUCrJ, 2014, 1, 49-60.

9. Crystal engineering in the Desiraju research group in Bangalore

Chakraborty, S., Dubey, R., Joseph, S., Mishra, M. K., Mukherjee, A., Siddiqui, K. A., Tothadi, S., Thakur, T. S., Varughese, S.

Cryst. Growth Des., 2012, 12, 4688-91.

8. Synthon identification in co-crystals and polymorphs with IR spectroscopy. Primary amides as a case study,

Mukherjee, A.,Tothadi, S., Chakraborty, S.; Ganguly, S.; Desiraju, G. R.*

CrystEngComm, 2013, 15, 4640-4654.

7. Polymorphs and hydrates of Etoricoxib, a selective COX-2 inhibitor

Grobelny, P., Mukherjee, A., Desiraju, G. R.*,

CrystEngComm, 2012, 14, 5785-5794.

6. Polymorphs, salts, and cocrystals: what’s in a name?

Aitipamula, S. et al.

Cryst. Growth Des., 2012, 12, 2147-52.

5. Halogen bonding and structural modularity in 2,3,4- and 3,4,5-trichlorophenol,

Mukherjee, A., Desiraju, G. R.*,

Cryst. Growth Des., 2011, 11, 3735-3739.

4. Drug-drug co-crystals: Temperature-dependent proton mobility in the molecular complex of isoniazid with 4-aminosalicylic acid

Grobelny, P., Mukherjee, A., Desiraju, G. R.*

CrystEngComm, 2011, 13, 4358-4364.

3. Shape and size mimicry in the design of ternary molecular solids: towards a robust strategy for crystal engineering

Tothadi, S., Mukherjee, A., Desiraju, G. R.*

Chem. Commun., 2011, 47, 12080-82

2. Polymorphs, pseudopolymorphs, and Co-crystals of orcinol: Exploring the structural landscape with high throughput crystallography

Mukherjee, A., Grobelny, P., Thakur, T. S., Desiraju, G. R.*

Cryst. Growth Des., 2011, 11, 2637-2653.

1. Synthon polymorphism and pseudopolymorphism in co-crystals. the 4,4′-bipyridine-4-hydroxybenzoic acid structural landscape

Mukherjee, A., Desiraju, G. R.*

Chem. Commun., 2011, 47, 4090-4092.