Deposition Number: 730192

Database Identifier: HULBEW

261. “Refined Syntheses of Hydrodipyrrin Precursors to Chlorin and Bacteriochlorin Building Blocks,” Krayer, M.; Balasubramanian, T.; Ruzié, C.; Ptaszek, M.; Cramer, D. L.; Taniguchi, M.; Lindsey, J. S. J. Porphyrins Phthalocyanines 2009, 13, 1098–1110. DOI: 10.1142/S1088424609001406

Deposition Number: 753822

Database Identifier: MUMGUX

260. “Synthesis and Photochemical Properties of 12-Substituted versus 13-Substituted Chlorins,” Mass, O.; Ptaszek, M.; Taniguchi, M.; Diers, J. R.; Kee, H. L.; Bocian, D. F.; Holten, D.; Lindsey, J. S. J. Org. Chem. 2009, 74, 5276–5289. DOI: 10.1021/jo900706x

Deposition Number: 753821

Database Identifier: MUMGOR

260. “Synthesis and Photochemical Properties of 12-Substituted versus 13-Substituted Chlorins,” Mass, O.; Ptaszek, M.; Taniguchi, M.; Diers, J. R.; Kee, H. L.; Bocian, D. F.; Holten, D.; Lindsey, J. S. J. Org. Chem. 2009, 74, 5276–5289. DOI: 10.1021/jo900706x

Deposition Number: 753820

Database Identifier: MUMGIL

260. “Synthesis and Photochemical Properties of 12-Substituted versus 13-Substituted Chlorins,” Mass, O.; Ptaszek, M.; Taniguchi, M.; Diers, J. R.; Kee, H. L.; Bocian, D. F.; Holten, D.; Lindsey, J. S. J. Org. Chem. 2009, 74, 5276–5289. DOI: 10.1021/jo900706x

Deposition Number: 753819

Database Identifier: MUMGEH

260. “Synthesis and Photochemical Properties of 12-Substituted versus 13-Substituted Chlorins,” Mass, O.; Ptaszek, M.; Taniguchi, M.; Diers, J. R.; Kee, H. L.; Bocian, D. F.; Holten, D.; Lindsey, J. S. J. Org. Chem. 2009, 74, 5276–5289. DOI: 10.1021/jo900706x

Deposition Number: 753818

Database Identifier: MUMGAD

260. “Synthesis and Photochemical Properties of 12-Substituted versus 13-Substituted Chlorins,” Mass, O.; Ptaszek, M.; Taniguchi, M.; Diers, J. R.; Kee, H. L.; Bocian, D. F.; Holten, D.; Lindsey, J. S. J. Org. Chem. 2009, 74, 5276–5289. DOI: 10.1021/jo900706x

Deposition Number: 662755

Database Identifier: TISPIV

230. “Synthesis and Structural Properties of Porphyrin Analogues of Bacteriochlorophyll c,” Ptaszek, M.; Yao, Z.; Dhanalekshmi, S.; Boyle, P. D.; Lindsey, J. S. Tetrahedron 2007, 63, 12629–12638. DOI: 10.1016/j.tet.2007.10.023

Deposition Number: 662534

Database Identifier: TISPER

230.  “Synthesis and Structural Properties of Porphyrin Analogues of Bacteriochlorophyll c,” Ptaszek, M.; Yao, Z.; Dhanalekshmi, S.; Boyle, P. D.; Lindsey, J. S. Tetrahedron 2007, 63, 12629–12638. DOI: 10.1016/j.tet.2007.10.023

Deposition Number: 666921

Database Identifier: XIPLEO

229. “Two Complementary Routes to 7-Substituted Chlorins.  Partial Mimics of Chlorophyll b,” Muthiah, C.; Ptaszek, M.; Nguyen, T. M.; Flack, K. M.; Lindsey, J. S. J. Org. Chem. 2007, 72, 7736–7749. DOI: 10.1021/jo701500d

Deposition Number: 663286

Database Identifier: VIPROC

223. “Design and synthesis of manganese porphyrins with tailored lipophilicity: Investigation of redox properties and superoxide dismutase activity,” Lahaye, D.; Muthukumaran, K.; Gryko, D.; Hung, C.-H.; Spasojevic, I.; Batinic-Haberle, I.; Lindsey, J. S. Bioorg. Med. Chem. 2007, 15, 7066–7086. DOI: 10.1016/j.bmc.2007.07.015

Deposition Number: 663285

Database Identifier: VIPRIW

223. “Design and synthesis of manganese porphyrins with tailored lipophilicity: Investigation of redox properties and superoxide dismutase activity,” Lahaye, D.; Muthukumaran, K.; Gryko, D.; Hung, C.-H.; Spasojevic, I.; Batinic-Haberle, I.; Lindsey, J. S. Bioorg. Med. Chem. 2007, 15, 7066–7086. DOI: 10.1016/j.bmc.2007.07.015

Deposition Number: 644305

Database Identifier: NIDFEM

213. “Sparsely substituted chlorins as core constructs in chlorophyll analogue chemistry. Part 3: Spectral and structural properties,” Taniguchi, M.; Ptaszek, M.; McDowell, B. E.; Boyle, P. D.; Lindsey, J. S. Tetrahedron 2007, 63, 3850–3863. DOI: 10.1016/j.tet.2007.02.040

Deposition Number: 644304

Database Identifier: NIDFAI

213. “Sparsely substituted chlorins as core constructs in chlorophyll analogue chemistry. Part 3: Spectral and structural properties,” Taniguchi, M.; Ptaszek, M.; McDowell, B. E.; Boyle, P. D.; Lindsey, J. S. Tetrahedron 2007, 63, 3850–3863. DOI: 10.1016/j.tet.2007.02.040

Deposition Number: 635679

Database Identifier: KEWFIC

208. “Masked Imidazolyl-Dipyrromethanes in the Synthesis of Imidazole-Substituted Porphyrins,” Bhaumik, J.; Yao, Z.; Borbas, K. E.; Taniguchi, M.; Lindsey, J. S. J. Org. Chem. 2006, 71, 8807–8817. DOI: 10.1021/jo061461r

Deposition Number: 623022

Database Identifier: KENZOT

205. “A New Route for Installing the Isocyclic Ring in Chlorins Yielding 13¹-Oxophorbines,” Laha, J. K.; Muthiah, C.; Taniguchi, M.; Lindsey, J. S. J. Org. Chem. 2006, 71, 7049–7052. DOI: 10.1021/jo0608265

Deposition Number: 1421175

Database Identifier: SUPHOC

193. “Alkylthio Unit as an α-Pyrrole Protecting Group for use in Dipyrromethane Synthesis,” Thamyongkit, P.; Bhise, A. D.; Taniguchi, M.; Lindsey, J. S. J. Org. Chem. 2006, 71, 903–910. DOI: 10.1021/jo051806q

Deposition Number: 289672

Database Identifier: VAWFAB

187. “Structural Control of the Photodynamics of Boron-Dipyrrin Complexes,” Kee, H. L.; Kirmaier, C.; Yu, L.; Thamyongkit, P.; Youngblood, W. J.; Calder, M. E.; Ramos, L.; Noll, B. C.; Bocian, D. F.; Scheidt, W. R.; Birge, R. R.; Lindsey, J. S.; Holten, D. J. Phys. Chem. B 2005, 109, 20433–20443. DOI: 10.1021/jp0525078

Deposition Number: 289671

Database Identifier: VAWDUT

187. “Structural Control of the Photodynamics of Boron-Dipyrrin Complexes,” Kee, H. L.; Kirmaier, C.; Yu, L.; Thamyongkit, P.; Youngblood, W. J.; Calder, M. E.; Ramos, L.; Noll, B. C.; Bocian, D. F.; Scheidt, W. R.; Birge, R. R.; Lindsey, J. S.; Holten, D. J. Phys. Chem. B 2005, 109, 20433–20443. DOI: 10.1021/jp0525078

Deposition Number: 289670

Database Identifier: VAWDON

187. “Structural Control of the Photodynamics of Boron-Dipyrrin Complexes,” Kee, H. L.; Kirmaier, C.; Yu, L.; Thamyongkit, P.; Youngblood, W. J.; Calder, M. E.; Ramos, L.; Noll, B. C.; Bocian, D. F.; Scheidt, W. R.; Birge, R. R.; Lindsey, J. S.; Holten, D. J. Phys. Chem. B 2005, 109, 20433–20443. DOI: 10.1021/jp0525078

Deposition Number: 289669

Database Identifier: VAWDIH

187. “Structural Control of the Photodynamics of Boron-Dipyrrin Complexes,” Kee, H. L.; Kirmaier, C.; Yu, L.; Thamyongkit, P.; Youngblood, W. J.; Calder, M. E.; Ramos, L.; Noll, B. C.; Bocian, D. F.; Scheidt, W. R.; Birge, R. R.; Lindsey, J. S.; Holten, D. J. Phys. Chem. B 2005, 109, 20433–20443. DOI: 10.1021/jp0525078

Deposition Number: 289668

Database Identifier: VAWDED

187. “Structural Control of the Photodynamics of Boron-Dipyrrin Complexes,” Kee, H. L.; Kirmaier, C.; Yu, L.; Thamyongkit, P.; Youngblood, W. J.; Calder, M. E.; Ramos, L.; Noll, B. C.; Bocian, D. F.; Scheidt, W. R.; Birge, R. R.; Lindsey, J. S.; Holten, D. J. Phys. Chem. B 2005, 109, 20433–20443. DOI: 10.1021/jp0525078

Deposition Number: 259519

Database Identifier: FANPOA

178. “9-Acylation of 1-Acyldipyrromethanes Containing a Dialkylboron Mask for the α-Acylpyrrole Motif,” Zaidi, S. H. H.; Muthukumaran, K.; Tamaru, S.-I.; Lindsey, J. S. J. Org. Chem. 2004, 69, 8356–8365. DOI: 10.1021/jo048587d

Deposition Number: 243057

Database Identifier: EZISOV

160. “A Tin-Complexation Strategy for Use with Diverse Acylation Methods in the Preparation of 1,9-Diacyldipyrromethanes,” Tamaru, S.-I.; Yu, L.; Youngblood, W. J.; Muthukumaran, K.; Taniguchi, M.; Lindsey, J. S. J. Org. Chem. 2004, 69, 765–777. DOI: 10.1021/jo035622s

Deposition Number: 243056

Database Identifier: EZISIP

160. “A Tin-Complexation Strategy for Use with Diverse Acylation Methods in the Preparation of 1,9-Diacyldipyrromethanes,” Tamaru, S.-I.; Yu, L.; Youngblood, W. J.; Muthukumaran, K.; Taniguchi, M.; Lindsey, J. S. J. Org. Chem. 2004, 69, 765–777. DOI: 10.1021/jo035622s

Deposition Number: 223851

Database Identifier: EMUKEC

148. “Excited-State Energy-Transfer Dynamics in Self-Assembled Triads Composed of Two Porphyrins and an Intervening Bis(dipyrrinato)metal Complex,” Yu, L.; Muthukumaran, K.; Sazanovich, I. V.; Kirmaier, C.; Hindin, E.; Diers, J. R.; Boyle, P. D.; Bocian, D. F.; Holten, D.; Lindsey, J. S. Inorg. Chem. 2003, 42, 6629–6647. DOI: 10.1021/ic034559m

Deposition Number: 1119659

Database Identifier: CAJVUF

120. “Synthesis of meso-Substituted Chlorins via Tetrahydrobilene-a Intermediates,” Taniguchi, M.; Ra, D.; Mo, G.; Balasubramanian, T.; Lindsey, J. S. J. Org. Chem. 2001, 66, 7342–7354. DOI: 10.1021/jo0104835

Deposition Number:  158848

Database Identifier: QEZCED

101. “Rational Synthesis of β-Substituted Chlorin Building Blocks,” Balasubramanian, T.; Strachan, J.-P.; Boyle, P. D.; Lindsey, J. S. J. Org. Chem. 2000, 65, 7919–7929. DOI: 10.1021/jo000913b

Deposition Number: 158850

Database Identifier: LAFYIA

65. “Refined Synthesis of 5-Substituted Dipyrromethanes,” Littler, B. J.; Miller, M. A.; Hung, C.-H.; Wagner, R. W.; O’Shea, D. F.; Boyle, P. D.; Lindsey, J. S. J. Org. Chem. 1999, 64, 1391–1396. DOI: 10.1021/jo982015+

Deposition Number: 158851

Database Identifier: LAGBUQ

65. “Refined Synthesis of 5-Substituted Dipyrromethanes,” Littler, B. J.; Miller, M. A.; Hung, C.-H.; Wagner, R. W.; O’Shea, D. F.; Boyle, P. D.; Lindsey, J. S. J. Org. Chem. 1999, 64, 1391–1396. DOI: 10.1021/jo982015+

Deposition Number: 1175505

Database Identifier: HEXZEP

34. “Synthesis of porphyrins tailored with eight facially-encumbering groups. An approach to solid-state light-harvesting complexes,” Wagner, R. W.; Lindsey, J. S.; Turowska-Tyrk, I.; Scheidt, W. R. Tetrahedron 1994, 50, 11097–11112. DOI: 10.1016/S0040-4020(01)89413-8