50
Prof. Debasish Haldar.
Bio-Organic Supramolecular chemistry Group.
Department of Chemical Sciences, IISER KOLKATA.
 50
50
h-index
27
i10-index
60
< <
Publications:
2024
159.
R. Tiwari, S. R. Chowdhury, N. Ghosh, D. Haldar and A. Banerjee.
JOURNAL OF LIGHTWAVE TECHNOLOGY, 2024.
Doi: 10.1109/JLT.2023.3339431.
2023
158.
A. Lal, M. Gumtya, and D. Haldar*
Trends in Organic Cheistry, 2023.
In Press.
157.
S. Mondal, M. Baidya, and D. Haldar*
Chemistry Select, 2023.
In Press.
156.
O. J. Ibukun, M. Gumtya, S. Singh, A. Shit and D. Haldar*
Soft Matter, 2023,19, 3215-3221.
Doi: 10.1039/d3sm00339f.
155.
O. J. Ibukun, M. Gumtya, S. Singh, A. Shit, M. Douzapau and D. Haldar*
Mol. Syst. Des. Eng., 2023, 8, 922-928.
Doi: 10.1039/d2me00273f.
154.
M. Douzapau, S. R. Chowdhury, S. Singh, O. J. Ibukun and D. Haldar*
Chemistry, 2023, 5(1), 691-702.
Doi.10.3390/chemistry5010048
153.
S. R. Chowdhury and D. Haldar*
Langmuir, 2023, 39, 13, 4855-4862.
Doi.10.1021/acs.langmuir.3c00456
152.
O. J. Ibukun, S. R. Chowdhury, S. Mondal and D. Haldar*
ChemBioChem, 2023, e202200758.
Doi.org/10.1002/cbic.202200758
151.
A. Shit, S. Singh, O. J. Ibukun, M. Gumtya and D. Haldar*
ACS Omega 2023, 8, 8712-8721
Doi.org/10.1021/acsomega.2c08092
150.
S. R. Chowdhury,# R. Tiwari,# N. Ghosh,* D. Haldar,* and A. Banerjee* (# = contributed equally to this work)
ACS Appl. Opt. Mater. 2023, 1, 2, 598-606
Doi.org/10.1021/acsaom.2c00156
149.
S. Roy,# S. Kumar Nandi,# D. Haldar,* and B. Pal* (# = contributed equally to this work)
Phys. Chem. Chem. Phys., 2023, 25, 5849-5856
Doi.org/10.1039/D2CP05462K
148.
S. Dey*, S. Sasmal, S. Mondal, S. Kumar, R. Chowdhury, D. Sarkar, C. Malla Reddy, L. Peters, G. Roth and D. Haldar
Acta Crystallographica Section B, 2023, B79.
Doi.org/10.1107/S2052520623000215
147.
S. Singh, A. Shit, S. Mondal, O. J. Ibukun and D. Haldar*
New J. Chem., 2023, 47, 1371.
https://doi.org/10.1039/D2NJ04782A
2022
146.
S. Kumar, S. R. Chowdhury, S. Mondal and D. Haldar*
Molecular Systems Design & Engineering, 2022.
Mol. Syst. Des. Eng., 2022. https://doi.org/10.1039/D2ME00190J
145.
S. Mondal, S. Shing, A. Shit, S. Kumar and D. Haldar*
New Journal of Chemistry, 2022.
New J. Chem., 2022,46, 14660-14666
144.
SYNTHESIS AND GELLING PERFORMANCES OF 4-BIPHENYLCARBOXY PROTECTED DIPEPTIDE.
P. Murmu, S. R. Chowdhury, and D. Haldar*
Journal of Molecular and Engineering Materials, 2022.
143.
Enhancing the optical response of bio-inspired peptide micro-waveguides exploiting chromatic aberration.
R. Tiwari, S. Roy, S. Mondal, N. Ghosh, D. Haldar,* Ayan Banerjee*
Journal of Biophotonics, 2022, 15.
142.
S. R. Chowdhury, S. K. Nandi and D. Haldar*
ACS Omega 2022, 7, 25, 21566-21573.
doi.org/10.1021/acsomega.2c01360
141.
S. R. Chowdhury and D. Haldar*
CrystEngComm, 2022,24, 4465-4470.
doi.org/10.1039/D2CE00462C
140.
S. Roy,# S. K. Nandi,# D. Haldar,* and Bipul Pal* (# = contributed equally to this work)
J. Mater. Chem. C, 2022,10, 8767-8775
doi.org/10.1039/D2TC00951J
139.
S. K. Nandi, R. Sarkar, A. Jaiswar, S. Roy,* D. Haldar*
ACS Omega 2022, 7, 20, 17245-17252.
doi.org/10.1021/acsomega.2c01168
138.
K. C. Hati,# S. Kumar,# S. Mondal, S. Singh, A. Shit, S. K. Nandia and D. Haldar* (# = contributed equally to this work)
Mater. Adv., 2022,3, 4194-4199
doi.org/10.1039/d2ma00084a
137.
S. Kumar, D. Haldar*
Journal of Molecular Chemistry, 22(1), 326-326.
136.
Bioinspired peptide-based thixotropic gel with anti-sticking effect against ice and water
K. C. Hati, S. Mondal, S. Kumar, S. R. Chowdhury, S. K. Nandi and D. Haldar*
Trends in Organic Chemistry, 2022
In Press
135.
D. Chattapadhyay, S. K. Nandi and D. Haldar*
Mater. Adv., 2022, 3, 2117
doi.org/10.1039/D1MA00992C
134.
S. K. Nandi, David Dìaz Dìaz*, and D. Haldar*
J. Phys. Chem. C 2022, 126, 1, 675-682
doi.org/10.1021/acs.jpcc.1c08659
133.
M. Gumtya, S. Mondal, S. Kumar, O. J. Ibukun and D. Haldar *
New J. Chem., 2022,46, 1105-1110
doi.org/10.1039/D1CE00738F
2021
132.
O. J. Ibukun, S. Mondal, S. Kumar and D. Haldar *
Chemistryselect, 2021, 6, 12736-12741.
doi.org/10.1002/slct.202103811
131.
S. K. Nandi, S. Mondal, S. Mondal, M. Gumtya and D. Haldar *
CrystEngComm, 2021, 23, 8093-8098.
DOI: 10.1039/D1CE00738F
130.
S. Roy Chowdhury, S. K. Nandi, S. Mondal, S. Kumar and D. Haldar *
Polymers 2021, 13, 2762.
DOI:10.3390/polym13162762
129.
Smart peptide assembly architectures to mimic biology’s adaptive properties and applications
Debasish Haldar
Molecular architectonics and Nanoarchitectonics, Springer, 2021
ISBN: 978-981-16-4188-6
128.
D. Chattapadhyay#, S. Mondal#, S. Kumar, and D. Haldar* (# = contributed equally to this work)
Chem Asian J. 2021, 16, 1-7.
DOI:10.1002/asia.202100590
127.
S. K. Nandi, S. Kumar, S. Roy Chowdhury, O. J. Ibukun, D. Haldar*
ChemistrySelect 2021, 6, 4448-4455.
DOI:10.1002/slct.202004726
126.
S. Mondal, D. Haldar*
New J. Chem., 2021,45, 4773-4779
DOI:10.1039/D0NJ05992G
125.
Amino acids and peptides in Colloidal Nanoparticle Synthesis, Reducing Agents in Colloidal Nanoparticle Synthesis
Debasish Haldar*
Royal Society of Chemistry,
ISBN 978-1-83916-165-0
124.
S. Kumar, S. Bera, S. K. Nandi, D. Haldar*
Soft Matter, 2021, 17, 113-119
DOI: 10.1039/D0SM01804J
2020
123.
S. Kumar, S. Bera, S. K. Nandi, D. Haldar*
Mater. Adv., 2020, 1, 3565-3571
DOI: 10.1039/D0MA00691B
122.
S. Kumar,S. K. Nandi, S. Suman, D. Haldar*
CrystEngComm, 2020, 22, 7975-7982
DOI: 10.1039/D0CE01199A
121.
S. K. Nandi, D. Haldar*
New J. Chem., 2020, 44, 17523-17530
DOI:10.1039/D0NJ03769A
120.
S. Mondal, D. Podder, S. K. Nandi, S. Roy Chowdhury, D. Haldar*
Soft Matter, 2020, 16, 10115-10121
DOI: 10.1039/d0sm00774a
119.
R. Tiwari, K. Maji, Ajmal, S. Ghosh, N. Ghosh*, D. Haldar* and A. Banerjee*
J. Mater. Chem. C, 2020,8, 9663-9670
DOI:10.1039/D0TC01510E
118.
Self-assembly and diverse applications of designer small peptides
D. Podder and Debasish Haldar
Lambert Academic Publishing, Germany, 2020
ISBN: 978-3-620-2-51775-1
117.
R. Sarkar, S. K. Nandi and D. Haldar*
Trends in Organic Chemistry, 2020, 20, 53-74
116.
Self-Assembly of Small Peptides and Peptide Mimetics: Single Crystal Analysis, Liquid and Single Crystals: Properties, Manufacturing and Uses
Debasish Haldar
Nova Science Publishers
ISBN: 978-1-53616-541-8
115.
D. Podder, S. Sasmal, S. Konar, P. Ghorai and Debasish Haldar*
Crystal Growth & Design, 2020, 20, 3, 1760-1770
DOI:10.1021/acs.cgd.9b01492
114.
S. K. Nandi, S. R. Chowdhury, D. Podder, P. Ghorai and Debasish Haldar*
Crystal Growth & Design, 2020, 20, 3, 1884-1890
DOI:10.1021/acs.cgd.9b01591
113.
S. R. Chowdhury, S. K. Nandi, D. Podder and Debasish Haldar*
ACS Omega 2020, 5, 2287-2294
DOI:10.1021/acsomega.9b03532
2019
112.
S. Sasmal, S. K. Nandi, S. Kumar and Debasish Haldar*
ChemistrySelect 2019, 4, 11172 - 11176
DOI: 10.1002/slct.201902815
111.
S. Sasmal, D. Podder, M. Debnath, S. K. Nandi and Debasish Haldar*
ChemistrySelect 2019, 4, 10302 - 10306
DOI: 10.1002/slct.201902353
110.
M. Debnath, S. Sasmal, D. Podder and Debasish Haldar*
ACS Omega 2019, 49, 13872-13878
DOI: 10.1021/acsomega.9b01393
109.
S. Sasmal,S. Roy Chowdhury, D. Podder and Debasish Haldar*
ACS Omega 2019, 48, 13172-13179
DOI: 10.1021/acsomega.9b01260
108.
S. Sasmal, K. Maji, David Dìaz Dìaz and Debasish Haldar*
CrystEngComm. 2019, 21, 4289-4297
DOI: 10.1039/C9CE00695H
107.
D. Podder, S. K. Nandi, S. Sasmal and Debasish Haldar*
Langmuir 2019, 35, 6453-6459
DOI: 10.1021/acs.langmuir.9b00456
106.
M. Häring, S. Grijalvo, Debasish Haldar, C. Saldìas, David Dìaz Dìaz
EPJ 2019, 115, 221-224.
DOI: 10.1016/j.eurpolymj.2019.03.044
105.
S. R. Chowdhury, Chidambaram C. T., D. Podder, S. Sasmal, M. Debnath, LA Kumaraswamidhas, Dr. S, Dutta. and Debasish Haldar*
ChemistrySelect 2019, 4, 2949-2953.
DOI: 10.1002/slct.201900293
104.
D. Podder, S. R. Chowdhury, S. K. Nandi and Debasish Haldar*
New J. Chem., 2019,43, 3743-3749.
DOI: 10.1039/C8NJ05578E
103.
E.M. Schon, C. Saldias, Debasish Haldar and David Diaz Diaz*
Macromol. Symp. 2018, 385, 1800193
DOI: 10.1039/C8NJ05578E
102.
M. Haring, S. K. Nandi, J. R. Lopez, D. Haldar, V. S. Martin, A. D. L.Gorrin, C. Saldias, and David Diaz Diaz*
ACS Omega., 2019, 4, 2111-2117.
DOI: 10.1021/acsomega.8b03292
101.
S. Sasmal, M. Debnath, S. K. Nandi and Debasish Haldar*
Nanoscale Advances, 2019, Accepted Manuscript.
DOI: 10.1039/C8NA00273H
100.
A. Paikar, D. Podder, S. Roy Chowdhury, S. Sasmal and Debasish Haldar*.
CrystEngComm.2019, 21, 589-593.
DOI: 10.1039/C8CE02086H
99.
M. Debnath, S. Sasmal, M. Abbasi, Rupak Datta* and Debasish Haldar*.
ChemistrySelect 2019, 4, 116-122
DOI: 10.1002/slct.201803229
2018
98.
Smart Functional Materials from Peptide Mimetic
K. Maji and Debasish Haldar*.
LAMBERT Academic Publishing
ISBN: 978-613-9-90870-7
97.
K. Maji, M. Abbasi, D. Podder, Rupak Datta* and Debasish Haldar*.
ChemistrySelect, 2018, 3 (36), 10220-10225
DOI: 10.1002/slct.201802002
96.
A. Paikar, T. Mondal, M. Debnath and Debasish Haldar*.
ChemistrySelect, 2018, 3 (33), 9576-9582
DOI: 10.1002/slct.201801133
95.
M. Debnath, T. Das, D. Podder, and Debasish Haldar*.
ACS Omega, 2018, 3 (8), 8760-8768
DOI: 10.1021/acsomega.8b00832
94.
S. K. Nandi, K. Maji, and Debasish Haldar*.
ACS Omega, 2018, 3 (4), 3744-3751
DOI: 10.1021/acsomega.8b00358
93.
A. Pramanik, M. Abbasi, K. Maji, S. K. Nandi, Rupak Datta* & Debasish Haldar*.
Chem. Select, 2018, 3, 393-398
DOI: 10.1002/slct.201702068
92.
T. Das, M. Haring, Debasish Haldar and David Diaz Diaz*.
Biomater. Sci., 2018, 6, 38-59
DOI: 10.1039/C7BM00882A
2017
91.
T. Das and Dr. Debasish Haldar*
ACS Omega, 2017, 2 (10), 6878-6887
DOI: 10.1021/acsomega.7b01379
90.
K. Maji and Dr. Debasish Haldar*
R. Soc. Open Sci, 2017, 4, 170684
DOI: 10.1098/rsos.170684
89.
A. Paikar and Dr. Debasish Haldar*
RSC. Adv, 2017, 7, 47170-47176
DOI: 10.1039/C7RA08035B
88.
M. Debnath, R. Sarkar, S. K. Nandi and Dr. Debasish Haldar*
Chem. Select, 2017, 2, 8146-8150
DOI: 10.1002/slct.201701577
87.
D. Podder, S. Bera, M. Debnath, T. Das and Debasish Haldar*
J. Materials. Chem. B, 2017, 5 , 7583-7590
DOI: 10.1039/C7TB01711A.
86.
K. Maji, S. Saha, R. Dey, Nirmalya Ghosh* and Debasish Haldar*.
J. Phys. Chem. C, 2017, 121, 19519-19529.
DOI: 10.1021/acs.jpcc.7b06725
85.
Halogen bond-mediated sheet-like assembly of core-substituted naphthalene bisimide and frabrication of paper strip sensor for fluoride.
A. Paikar and Debasish Haldar*.
Trends in Organic Chemistry, 2017, 18, 85-95.
84.
S. Sasmal and Dr. Debasish Haldar*.
Chemistry Select, 2017, 2, 5832-5837.
DOI: 10.1002/slct.201851218
83.
Debasish Haldar*
Advances in Nanotechnology. Vol-19, Nova Publication, 2017.
ISBN: 978-1-53612-421-7
82.
M. Debnath, S. Sasmal and Debasish Haldar*.
J. Mat. Chem B, 2017, 5, 5450-5457.
DOI: 10.1039/C7TB00025A
81.
K. Maji and Debasish Haldar*.
ACS Omega 2017, 2, 1938-1946.
DOI: 10.1021/acsomega.7b00234
80.
A. Paikar, M. Debnath, D. Podder, S. Sasmal and Debasish Haldar*.
Org. Biomol. Chem., 2017, 15, 4218-4225.
DOI: 10.1039/c7ob00797c
79.
T. Das, A. Pramanik and Debasish Haldar*.
Scientific Reports, 2017, 7, 40485.
DOI: 10.1038/srep40465.
78.
A. Pramanik and Debasish Haldar*.
RSC Advances, 2017, 7, 389-395.
DOI: 10.1039/C6RA24799G.
77.
A. Paikar, A. Pramanik, T. Das and Debasish Haldar*.
Polymer Chemistry, 2017, 8, 396-403.
DOI: 10.1039/C6PY01955B.
2016
76.
A. Pramanik, A. Paikar, K. Maji and Debasish Haldar*.
RSC Advances, 2016, 6, 59851-59857.
DOI: 10.1039/C6RA13026G.
75.
D. Podder, S. Sasmal, K. Maji and Debasish Haldar*.
CrystEngComm, 2016, 18, 4109-4114.
DOI: 10.1039/C5CE02005K.
74.
R. Sarkar, S. Sasmal, D. Podder and Debasish Haldar*.
Macromolecular Symposia, 2016, 369, 67-73.
DOI: 10.1002/masy.201600061.
73.
Porous Organic Materials from Self-Assembly of Peptides and Polyamides.
Debasish Haldar*.
Chapter 24, Encyclopedia of Physical Organic Chemistry, Editor Zerong Wang, Wiley Inc. 2016.
ISBN-13: 978-1118485459.
72.
S. Bera and Debasish Haldar*.
Journal of Materials Chemistry A, 2016, 4, 6933-6939.
DOI: 10.1039/C5TA08010J.
71.
A. Pramanik, A. Paikar, T. Das, K. Maji and Debasish Haldar*.
RSC Advances, 2016, 6, 39172 - 39179.
DOI: 10.1039/C5TA08010J.
70.
Debasish Haldar*.
Chapter 3, Nanotechnology Science and Technology, Nova Publication, 2016.
ISBN: 978-1-63485-415-3
2015
69.
R. Sarkar, M. Debnath, K. Maji and Debasish Haldar*.
RSC Advances, 2015, 5, 76257-76262.
DOI: 10.1039/C5RA12831E
68.
R. Sarkar, K. Maji and Debasish Haldar*.
RSC Advances, 2015, 5, 59585 59600.
DOI: 10.1039/C5RA12831E
67.
S. Bera, D. K. S. Ambast, B. Pal and Debasish Haldar*.
PCCP, 2015, 17, 16983-16990.
DOI: 10.1039/C5CP02218E
66.
A. Pramanik, A. Paikar and Debasish Haldar*.
RSC Adv., 2015, 5, 53886-53892.
DOI: 10.1039/C5RA07864D
65.
A. Paikar, A. Pramanik and Debasish Haldar*.
RSC Advances, 2015, 5, 31845 - 31851.
DOI: 10.1039/C5RA03864B
64.
D. Podder, S. Sasmal and Debasish Haldar*.
Current Organic Synthesis, 2015, 12, 440-456.
DOI: 10.2174/1585179412666150224235413
63.
S. Bera, S. Maity and Debasish Haldar*.
CrystEngComm, 2015, 17, 1569-1600.
DOI: 10.1039/C4CE01950D
2014
62.
K. Maji, R. Sarkar, S. Bera and Debasish Haldar*.
Chem. Commun., 2014, 50, 12749-12752.
DOI: 10.1039/C4CC04475D
61.
P. Jana, S. Bera, A. Paikar and Debasish Haldar*.
Crystal Growth and Design, 2014, 14, 3918-3922.
DOI: 10.1021/cg500501r
60.
S. Bera, S. K. Maity and Debasish Haldar*.
CrystEngComm, 2014, 16, 4834-4841.
DOI: 10.1039/C3CE42582G
59.
S. Bera, P. Jana, S. K. Maity, and Debasish Haldar*.
Crystal Growth and Design, 2014, 14, 1032-1038.
DOI: 10.1039/C3CE42582G
58.
S. K. Maity, S. Bera, A. Paikar, A. Pramanik and Debasish Haldar*.
CrystEngComm, 2014, 16, 2527-2534.
DOI: 10.1039/C3CE41796D
57.
P. Jana, A. Paikar, S. Bera, S. K. Maity and Debasish Haldar*.
Organic Letters, 2014, 16, 3841.
DOI: 10.1021/ol402865t
2013
56.
S. K. Maity, S. Bera, A. Paikar, A. Pramanik and Debasish Haldar*.
Chem. Commun., 2013, 49 9051-9053.
DOI: 10.1039/C3CC44231D
55.
Structural and photoelectrochemical properties of quantum dots embedded peptide matrix nanocomposites, in Handbook of Functional Nanomaterials. Volume 3-Application and Development.
Debasish Haldar*.
Nova publication, USA, 2013.
ISBN: 978-1-62948-566-9
54.
S. K. Maity, S. Bera, A. Paikar, A. Pramanik and Debasish Haldar*.
CrystEngComm, 2013, 15, 5860-5866.
DOI: 10.1039/C3CE40689J
53.
Debasish Haldar*.
Lambert Academic Publishing, Germany, 2013.
ISBN 978-3-859-37523-1
52.
S. K. Maity, S. Bera and Debasish Haldar*.
Current Organic Synthesis, 2013, 10, 525-546.
DOI: 10.2174/1585179411310040002
51.
P. Jana, S. K. Maity, S. Bera, P. K. Ghorai and Debasish Haldar*.
CrystEngComm, 2013, 15, 2512-2518.
DOI: 10.1039/C3CE26700H
50
S. Maity, R. Kumar, S. K. Maity, P. Jana, S. Bera and Debasish Haldar*.
Medicinal Chemistry Communications, 2013, 4, 525-536.
DOI: 10.1039/C2MD20236K
2012
49.
P. Jana, S. Maity and Debasish Haldar*.
Advances in Organic Synthesis, 2012, Vol. 5, 546-569.
DOI: 10.2174/9781608054800113050010
48.
S. K. Maity, R. Kumar, D. K. S. Ambast, B. Pal* and Debasish Haldar*.
J. Mater. Chem., 2012, 22, 22198-22203.
DOI: 10.1039/C2JM34338J
47.
Debasish Haldar*.
Advances in Organic Synthesis, 2012, Vol. 5, 495-545.
DOI: 10.2174/9781608050291113060010
46.
P. Jana, S. Maity, S. K. Maity, P. K. Ghoraia and Debasish Haldar*.
CrystEngComm, 2012, 14, 8586-8592.
DOI: 10.1039/C2CE25778E
45.
S. Maity, S. Sarkar, P. Jana, S. K. Maity, S. Bera, V. Mahalingam* and Debasish Haldar*.
Soft Matter, 2012, 8, 7960-7966.
DOI: 10.1039/C2SM25981H
44.
S. K. Maity, S. Maity, P. Jana and Debasish Haldar*.
CrystEngComm, 2012, 14, 4034-4040.
DOI: 10.1039/C2CE05786G
43.
P. Jana, S. Maity, S. K. Maity, P. K. Ghorai and Debasish Haldar*..
Soft Matter, 2012, 8, 5621-5628.
DOI: 10.1039/C2SM25062D
42.
S. K. Maity, S. Maity, P. Jana, and Debasish Haldar*.
CrystEngComm, 2012, 14, 3156-3162.
DOI: 10.1039/C2CE06355G
41.
Amyloid-like fibril-forming supramolecular cross β-structure of a model peptide: a crystallographic insight.
Debasish Haldar*.
Lambert Academic Publishing, Germany, 2012.
ISBN: 978-3-8473-7142-7.
40.
S. Maity, P. Jana, S. K. Maity, P. kumar and Debasish Haldar*.
Crystal Growth and Design, 2012, 12, 422-428.
DOI: 10.1021/cg201268x
39.
S. K. Maity, S. Maity, P. Jana and Debasish Haldar*.
Chem. Commun., 2012, 48, 711-713.
DOI: 10.1039/C1CC15585A
2011
38.
S. Maity, P. Jana, S. K. Maity and Debasish Haldar*.
Soft Matter, 2011, 7, 10174-10181.
DOI: 10.1039/C1SM05958K
37.
Supramolecular helices form self-assembled short peptides.
Debasish Haldar*.
Nova publication, USA, 2011.
ISBN: 978-1-61122-690-4.
36.
S. Maity, P. Kumar and Debasish Haldar*.
Soft Matter, 2011, 7, 5239 - 5245.
DOI: 10.1039/C1SM05277B
35.
P. Jana, S. Maity, S. K. Maity and Debasish Haldar*.
Chem. Commun., 2011, 47, 2092-2094.
DOI: 10.1039/C0CC04244G
34.
S. Maity, P. Jana and Debasish Haldar*.
CrystEngComm, 2011, 13, 3064-3071.
DOI: 10.1039/C0CE00851C
33.
S. Maity, P. Kumar and Debasish Haldar*.
Org. Biomol. Chem., 2011, 9, 3787 - 3791.
DOI: 10.1039/C0OB01033B
32.
S. Maity, P. Jana, S. K. Maity and Debasish Haldar*.
Langmuir, 2011, 27, 3835-3841.
DOI: 10.1021/la104461m
31.
P. Jana, S. Maity and Debasish Haldar*.
CrystEngComm, 2011, 13, 973-978.
DOI: 10.1039/C0CE00143K
2010
30.
P. Jana, S. Maity and Debasish Haldar*.
Current Organic Synthesis, 2010, 7, 224-234.
DOI: 10.2174/158517910791162995
29.
B. Baptiste, J. Zhu, Debasish Haldar, B. Kauffmann, J.-M. Léger and Ivan Huc*.
Chem. Asian J., 2010, 5, 1364-1375.
DOI: 10.1002/asia.200900713
2009
28.
Debasish Haldar and Carsten Schmuck*.
Chem. Soc. Rev., 2009, 2, 363-371.
DOI: 10.1039/B803553A
2008
27.
Debasish Haldar*.
Current Organic Synthesis, 2008, 5, 61-80.
DOI: 10.2174/158517908783497527
26.
Debasish Haldar*.
Tetrahedron, 2008, 64, 186-190.
DOI: 10.1016/j.tet.2007.10.074
2007
25.
Debasish Haldar, H. Jiang, J.-M. Léger and I. Huc*.
Tetrahedron 2007, 63, 6322-6330.
DOI: 10.1016/j.tet.2007.02.114
24.
Debasish Haldar* and A. Banerjee*.
Int. J. Pept. Res. Thept. 2007, 13, 439-446.
DOI: 10.1007/s10989-006-9072-x
23.
Debasish Haldar*, M. G. B. Drew and A. Banerjee*.
Tetrahedron 2007, 63, 5561-5566.
DOI: 10.1016/j.tet.2007.04.026
2006
22.
Debasish Haldar, H. Jiang, J.-M. Léger and I. Huc*.
Angew. Chem. Int. Ed., 2006, 45, 5483-5486.
DOI: 10.1002/anie.200600698
21.
Debasish Haldar*, M. G. B. Drew and A. Banerjee*.
Tetrahedron 2006, 62, 6385-6378.
DOI: 10.1016/j.tet.2006.04.036
20.
Debasish Haldar* and A. Banerjee*.
Int. J. Pept. Res. Thept. 2006, 12, 341-348.
DOI: 10.1007/s10989-006-9037-0
2005
19.
X-ray crystallographic signature of supramolecular triple helix formation from a water soluble synthetic tetrapeptide.
A. K. Das, Debasish Haldar, R. P. Hegde, N. Shamala and A. Banerjee.
Chem. Commun. 2005.
DOI: 10.1039/B417726F
18.
Can a consecutive double turn conformation be considered as a peptide based molecular scaffold for supramolecular helix in the solid state?
A. K. Das, A. Banerjee, M. G. B. Drew, S. Ray, Debasish Haldar and A. Banerjee.
Tetrahedron 2005, 61, 5027-5036
DOI: 10.1016/j.tet.2005.03.057
17.
The role of disulfide bond in amyloid-like fibrillogenesis in a model peptide system.
A. K. Das, M. G. B. Drew, Debasish Haldar and A. Banerjee.
Org. Biomol. Chem. 2005, 3, 3502-3507.
DOI: 10.1039/B509083K
16.
Peptide-assisted synthesis of gold nanoparticles and their self-assembly.
R. R. Bhattacharjee, A. K. Das, Debasish Haldar, S. Si, A. Banerjee, and T. K. Mandal.
J. Nanosci. Nanotech. 2005, 5, 1141 -1147.
2004
15.
Self-assembly of b-turn forming synthetic tripeptides into supramolecular b-sheets and amyloid-like fibrils in the solid state.
S. K. Maji, Debasish Haldar, M. G. B. Drew, A. Banerjee, A. K. Das and A. Banerjee.
Tetrahedron 2004, 60, 3251-3259.
14.
Hydrogen-bonded dimer can mediate supramolecular b-sheet formation and subsequent amyloid-like fibril formation: a model study.
A. Banerjee, S. K. Maji, M. G. B. Drew, Debasish Haldar, A. K. Das and A. Banerjee.
Tetrahedron 2004, 60, 5935-5944.
13.
Stepwise self-assembly of a tripeptide from molecular dimers to supramolecular b-sheets in crystals and amyloid-like fibrils in the solid state.
A. K. Das, A. Banerjee, M. G. B. Drew, Debasish Haldar and A. Banerjee.
Supramolecular Chemistry 2004, 16, 331-335.
12.
A new motif in the formation of peptide nanotubes: the crystallographic signature.
S. Ray, Debasish Haldar, M. G. B. Drew and A. Banerjee.
Org. Lett. 2004, 6, 4463-4465.
2003
11.
Supramolecular peptide helix from a novel double turn forming peptide containing a β-amino acid.
A. Banerjee, S. K. Maji, M. G. B. Drew, Debasish Haldar, and A. Banerjee.
Tetrahedron Lett. 2003, 44, 699-702.
10.
Conformational heterogeneity of a turn mimetic pseudo-peptide: comparison of crystal state, solution and theoretically derived structures.
S. K. Maji, Debasish Haldar, D. Bhattacharyya and A. Banerjee.
J. Mol. Struct. 2003, 646, 111-123.
9.
First crystallographic signature of an acyclic peptide nanorod: molecular mechanism of nanorod formation by a self-assembled tetrapeptide.
Debasish Haldar, A. Banerjee, M. G. B. Drew, A. K. Das and A. Banerjee.
Chem. Commun. 2003, 1406-1407.
8.
Amyloid-like fibril-forming supramolecular β-sheets from a β-turn forming tripeptide containing non-coded amino acids: the Crystallographic signature.
A. Banerjee, S. K. Maji, M. G. B. Drew, Debasish Haldar and A. Banerjee.
Tetrahedron Lett. 2003, 44, 335-339.
7.
Conformational heterogeneity of a tripeptide in the solid state and in solution: characterization of a g-turn containing incipient hairpin in solution.
S. K. Maji, Debasish Haldar, A. Banerjee, C. Mukhopadhyay and A. Banerjee.
J. Struct. Chem. 2003, 44, 860-864.
6.
An amyloid-like fibril forming antiparallel supramolecular b-sheet from a synthetic tripeptide: a crystallographic signature.
A. Banerjee, S. K. Maji, M. G. B. Drew, Debasish Haldar and A. Banerjee.
Tetrahedron Lett. 2003, 44, 6741-6744.
2002
5.
First crystallographic signature of the highly ordered supramolecular helical assemblage from a tripeptide containing a non-coded amino acid.
Debasish Haldar, S. K. Maji, W. S. Sheldrick and A. Banerjee.
Tetrahedron Letters 2002, 43, 2653-2656.
4.
A unique example of a pseudo-peptide containing noncoded amino acids self-assembling into a supramolecular b-sheet-like structure in crystals.
S. K. Maji, Debasish Haldar, D. Velmurugan, V. Rajakannan and A. Banerjee.
Lett. Pept. Sci. 2002, 8, 61-67.
3.
Self-assembly of a short peptide monomer into a continuous hydrogen bonded supramolecular helix: the crystallographic signature.
Debasish Haldar, S. K. Maji, M. G. B. Drew, A. Banerjee and A. Banerjee.
Tetrahedron Lett. 2002, 43, 5465-5468.
2.
Fibril-forming model synthetic peptides containing 3-aminophenylacetic acid.
S. K. Maji, Debasish Haldar, A. Banerjee and A. Banerjee.
Tetrahedron 2002, 58, 8695-8702.
1.
Self-Assembly of a tetrapeptide in which a unique supramolecular helical structure is formed via intermolecular hydrogen bonding in the solid state.
S. K. Maji, A. Banerjee, M. G. B. Drew, Debasish Haldar and A. Banerjee.
Tetrahedron Lett. 2002, 43, 6759-6762.
50
IISER Kolkata.
Main Campus, Mohanpur,
Nadia - 741246, W.B. India.
 50 50