2010–2015

Deposition Number: 1052029

Database Identifier: UYITIH

333.  "Elaboration of an Unexplored Substitution Site in Synthetic Bacteriochlorins," Zhang, N.; Reddy, K. R.; Jiang, J.; Taniguchi, M.; Sommer, R. D.; Lindsey, J. S. J. Porphyrins Phthalocyanines 2015, 19, 887–902. DOI: 10.1142/S1088424615500534 

Deposition Number: 1029006

Database Identifier: UYIPEZ

327. "Progress Towards Synthetic Chlorins with Graded Polarity, Conjugatable Substituents, and Wavelength Tunability," Ra, D.; Gauger, K. A.; Muthukumaran, K.; Balasubramanian, T.; Chandrashaker, V.; Taniguchi, M.; Yu, Z.; Talley, D. C.; Ehudin, M.; Ptaszek, M.; Lindsey, J. S. J. Porphyrins Phthalocyanines 2015, 19, 547–572. DOI: 10.1142/S1088424615500042

Deposition Number: 978333

Database Identifier: VISYUT

313. "Synthesis of 24 Bacteriochlorin Isotopologues, Each Containing a Symmetrical Pair of 13C or 15N Atoms in the Inner Core of the Macrocycle," Chen, C.-Y.; Bocian, D. F.; Lindsey, J. S. J. Org. Chem. 2014, 79, 1001–1016. DOI: 10.1021/jo402488n

Deposition Number: 974412

Database Identifier: LIXLUB

317. "Regioselective β-Pyrrolic Bromination of Hydrodipyrrin–Dialkylboron Complexes Facilitates Access to Synthetic Models for Chlorophyll f," Liu, M.; Ptaszek, M.; Mass, O.; Minkler, D. F.; Sommer, R. D.; Bhaumik, J.; Lindsey, J. S. New J. Chem. 2014, 38, 1717–1730.DOI: 10.1039/C3NJ01508D

Deposition Number: 974411

Database Identifier: LIXLOV

317. "Regioselective β-Pyrrolic Bromination of Hydrodipyrrin–Dialkylboron Complexes Facilitates Access to Synthetic Models for Chlorophyll f," Liu, M.; Ptaszek, M.; Mass, O.; Minkler, D. F.; Sommer, R. D.; Bhaumik, J.; Lindsey, J. S. New J. Chem. 2014, 38, 1717–1730. DOI: 10.1039/C3NJ01508D

Deposition Number: 974410

Database Identifier: LIXDON

317. "Regioselective β-Pyrrolic Bromination of Hydrodipyrrin–Dialkylboron Complexes Facilitates Access to Synthetic Models for Chlorophyll f," Liu, M.; Ptaszek, M.; Mass, O.; Minkler, D. F.; Sommer, R. D.; Bhaumik, J.; Lindsey, J. S. New J. Chem. 2014, 38, 1717–1730. DOI: 10.1039/C3NJ01508D

Deposition Number: 974409

Database Identifier: LIXLIP

317. "Regioselective β-Pyrrolic Bromination of Hydrodipyrrin–Dialkylboron Complexes Facilitates Access to Synthetic Models for Chlorophyll f," Liu, M.; Ptaszek, M.; Mass, O.; Minkler, D. F.; Sommer, R. D.; Bhaumik, J.; Lindsey, J. S. New J. Chem. 2014, 38, 1717–1730. DOI: 10.1039/C3NJ01508D

Deposition Number: 958397

Database Identifier: MIQHOL

312. "Hydrophilic Tetracarboxy Bacteriochlorins for Photonics Applications," Jiang, J.; Vairaprakash, P.; Reddy, K. R.; Sahin, T.; Pavan, M. P.; Lubian, E.; Lindsey, J. S. Org. Biomol. Chem. 2014, 12, 86–103. DOI: 10.1039/C3OB41791C

Deposition Number: 958396

Database Identifier: MIQHUR

312. "Hydrophilic Tetracarboxy Bacteriochlorins for Photonics Applications," Jiang, J.; Vairaprakash, P.; Reddy, K. R.; Sahin, T.; Pavan, M. P.; Lubian, E.; Lindsey, J. S. Org. Biomol. Chem. 2014, 12, 86–103. DOI: 10.1039/C3OB41791C

Deposition Number: 941758

Database Identifier: NIGTUU

309. "Serendipitous Synthetic Entrée to Tetradehydro Analogues of Cobalamins," Deans, R. M.; Mass, O.; Diers, J. R.; Bocian, D. F.; Lindsey, J. S. New J. Chem. 2013, 37, 3964–3975. DOI: 10.1039/C3NJ00574G

Deposition Number: 919107

Database Identifier: BENRET

294. “Synthesis and Physicochemical Properties of Metallobacteriochlorins,” Chen, C.-Y.; Sun, E.; Fan, D.; Taniguchi, M.; McDowell, B. E.; Yang, E.; Diers, J. R.; Bocian, D. F.; Holten, D.; Lindsey, J. S. Inorg. Chem. 2012, 51, 9443–9464. DOI: 10.1021/ic301262k

Deposition Number: 919106

Database Identifier: BENRIX

294. “Synthesis and Physicochemical Properties of Metallobacteriochlorins,” Chen, C.-Y.; Sun, E.; Fan, D.; Taniguchi, M.; McDowell, B. E.; Yang, E.; Diers, J. R.; Bocian, D. F.; Holten, D.; Lindsey, J. S. Inorg. Chem. 2012, 51, 9443–9464. DOI: 10.1021/ic301262k

Deposition Number: 919105

Database Identifier: BENROD

294. “Synthesis and Physicochemical Properties of Metallobacteriochlorins,” Chen, C.-Y.; Sun, E.; Fan, D.; Taniguchi, M.; McDowell, B. E.; Yang, E.; Diers, J. R.; Bocian, D. F.; Holten, D.; Lindsey, J. S. Inorg. Chem. 2012, 51, 9443–9464. DOI: 10.1021/ic301262k

Deposition Number: 881530

Database Identifier: NEJMIA

293. “Competing Knorr and Fischer-Fink Pathways to pyrroles in neutral aqueous solution,” Chandrashaker, V.; Taniguchi, M.; Ptaszek, M.; Lindsey, J. S. Tetrahedron 2012, 68, 6957–6967. DOI: 10.1016/j.tet.2012.05.080

Deposition Number: 881529

Database Identifier: NEJMEW

293. “Competing Knorr and Fischer-Fink Pathways to pyrroles in neutral aqueous solution,” Chandrashaker, V.; Taniguchi, M.; Ptaszek, M.; Lindsey, J. S. Tetrahedron 2012, 68, 6957–6967. DOI: 10.1016/j.tet.2012.05.080

Deposition Number: 809306

Database Identifier: OTIXUL

279. “Faile Synthesis of a B,D-Tetradehydrocorrin and Rearrangement to Bacteriochlorins,” Aravindu, K.; Krayer, M.; Kim, H.-J.; Lindsey, J. S. New J. Chem. 2011, 35, 1376–1384. DOI: 10.1039/c1nj20027e

Deposition Number: 769377

Database Identifier: PACSAP

270. “Structural Studies of Sparsely Substituted Chlorins and Phorbines Establish Benchmarks for Changes in the Ligand Core and Framework of Chlorophyll Macrocycles,” Taniguchi, M.; Mass, O.; Boyle, P. D.; Tang, Q.; Diers, J. R.; Bocian, D. F.; Holten, D.; Lindsey, J. S. J. Mol. Structure 2010, 979, 27–45. DOI: 10.1016/j.molstruc.2010.05.035

Deposition Number: 769376

Database Identifier: PACRUI

270. “Structural Studies of Sparsely Substituted Chlorins and Phorbines Establish Benchmarks for Changes in the Ligand Core and Framework of Chlorophyll Macrocycles,” Taniguchi, M.; Mass, O.; Boyle, P. D.; Tang, Q.; Diers, J. R.; Bocian, D. F.; Holten, D.; Lindsey, J. S. J. Mol. Structure 2010, 979, 27–45. DOI: 10.1016/j.molstruc.2010.05.035

Deposition Number: 769375

Database Identifier: PACROC

270. “Structural Studies of Sparsely Substituted Chlorins and Phorbines Establish Benchmarks for Changes in the Ligand Core and Framework of Chlorophyll Macrocycles,” Taniguchi, M.; Mass, O.; Boyle, P. D.; Tang, Q.; Diers, J. R.; Bocian, D. F.; Holten, D.; Lindsey, J. S. J. Mol. Structure 2010, 979, 27–45. DOI: 10.1016/j.molstruc.2010.05.035

Deposition Number: 769374

Database Identifier: PACRIW

270. “Structural Studies of Sparsely Substituted Chlorins and Phorbines Establish Benchmarks for Changes in the Ligand Core and Framework of Chlorophyll Macrocycles,” Taniguchi, M.; Mass, O.; Boyle, P. D.; Tang, Q.; Diers, J. R.; Bocian, D. F.; Holten, D.; Lindsey, J. S. J. Mol. Structure 2010, 979, 27–45. DOI: 10.1016/j.molstruc.2010.05.035

Deposition Number: 769373

Database Identifier: PACRES

270. “Structural Studies of Sparsely Substituted Chlorins and Phorbines Establish Benchmarks for Changes in the Ligand Core and Framework of Chlorophyll Macrocycles,” Taniguchi, M.; Mass, O.; Boyle, P. D.; Tang, Q.; Diers, J. R.; Bocian, D. F.; Holten, D.; Lindsey, J. S. J. Mol. Structure 2010, 979, 27–45. DOI: 10.1016/j.molstruc.2010.05.035

Deposition Number: 812864

Database Identifier: OKUNAK

265. “Expanded Scope of Synthetic Bacteriochlorins via Improved Acid Catalysis Conditions and Diverse Dihydrodipyrrin-Acetals,” Krayer, M.; Ptaszek, M.; Kim, H.-J.; Meneely, K. R.; Fan, D.; Secor, K.; Lindsey, J. S. J. Org. Chem. 2010, 75, 1016–1039. DOI: 10.1021/jo9025572

Deposition Number: 812175

Database Identifier: OJOXUH

267. “De Novo Synthesis of Long-Wavelength Absorbing Chlorin-13,15-Dicarboximides,” Ptaszek, M.; Lahaye, D.; Krayer, M.; Muthiah, C.; Lindsey, J. S. J. Org. Chem. 2010, 75, 1659–1673. DOI: 10.1021/jo902649d

Deposition Number: 812174

Database Identifier: OJOXOB

267. “De Novo Synthesis of Long-Wavelength Absorbing Chlorin-13,15-Dicarboximides,” Ptaszek, M.; Lahaye, D.; Krayer, M.; Muthiah, C.; Lindsey, J. S. J. Org. Chem. 2010, 75, 1659–1673. DOI: 10.1021/jo902649d

Deposition Number: 812173

Database Identifier: OJOXIV

267. “De Novo Synthesis of Long-Wavelength Absorbing Chlorin-13,15-Dicarboximides,” Ptaszek, M.; Lahaye, D.; Krayer, M.; Muthiah, C.; Lindsey, J. S. J. Org. Chem. 2010, 75, 1659–1673. DOI: 10.1021/jo902649d