Crystal Structures
2020–2021
16 structures
Deposition Number: 2086067
Database Identifier: IZITET
414. “Synthesis of AD-Dihydrodipyrrins Equipped with Latent Substituents of Native Chlorophylls and Bacteriochlorophylls,” Wang, P.; Lindsey, J. S. J. Org. Chem. 2021, 86, 11794–11811. DOI: 10.1021/acs.joc.1c01239
Deposition Number: 2086066
Database Identifier: IZITAP
414. “Synthesis of AD-Dihydrodipyrrins Equipped with Latent Substituents of Native Chlorophylls and Bacteriochlorophylls,” Wang, P.; Lindsey, J. S. J. Org. Chem. 2021, 86, 11794–11811. DOI: 10.1021/acs.joc.1c01239
Deposition Number: 2086065
Database Identifier: IZISUI
414. “Synthesis of AD-Dihydrodipyrrins Equipped with Latent Substituents of Native Chlorophylls and Bacteriochlorophylls,” Wang, P.; Lindsey, J. S. J. Org. Chem. 2021, 86, 11794–11811. DOI: 10.1021/acs.joc.1c01239
Deposition Number: 2083661
Database Identifier: OXIJUD
413. “Synthesis of model bacteriochlorophylls containing substituents of native rings A, C and E,” Chung, D. T. M.; Tran, P. V.; Chau Nguyen, K.; Wang, P.; Lindsey, J. S. New J. Chem. 2021, 45, 13302–13316. DOI: 10.1039/D1NJ02469H
Deposition Number: 2083660
Database Identifier: OXIJOX
413. “Synthesis of model bacteriochlorophylls containing substituents of native rings A, C and E,” Chung, D. T. M.; Tran, P. V.; Chau Nguyen, K.; Wang, P.; Lindsey, J. S. New J. Chem. 2021, 45, 13302–13316. DOI: 10.1039/D1NJ02469H
Deposition Number: 2083659
Database Identifier: OXIJIR
413. “Synthesis of model bacteriochlorophylls containing substituents of native rings A, C and E,” Chung, D. T. M.; Tran, P. V.; Chau Nguyen, K.; Wang, P.; Lindsey, J. S. New J. Chem. 2021, 45, 13302–13316. DOI: 10.1039/D1NJ02469H
Deposition Number: 2083658
Database Identifier: OXIJEN
413. “Synthesis of model bacteriochlorophylls containing substituents of native rings A, C and E,” Chung, D. T. M.; Tran, P. V.; Chau Nguyen, K.; Wang, P.; Lindsey, J. S. New J. Chem. 2021, 45, 13302–13316. DOI: 10.1039/D1NJ02469H
Deposition Number: 1956625
Database Identifier: ZACTAC
395. "Fourfold alkyl wrapping of a Copper(II) Porphyrin Thwarts Macrocycle π–π stacking in a compact supramolecular package," Nalaoh, P.; Bureekaew, S.; Promarak, V.; Lindsey, J. S. Acta Cryst. C 2020, C76, 647–654. DOI: 10.1107/S2053229620007172
Deposition Number: 1999189
Database Identifier: WUXLAF
394. "Crystal Structure of 1,9-Dibromo-5-phenyldipyrrin, Tetrapyrrole Synthesis Derivative and Free Base Ligand of BODIPY Building Blocks," O’Shea, D. F.; Sommer, R. D.; Taniguchi, M.; Lindsey, J. S. X-Ray Struct. Anal. Online 2020, 36, 21–22. DOI: 10.2116/xraystruct.36.21
Deposition Number: 1988555
Database Identifier: DURMIP
392. "Asymmetric Synthesis of a Bacteriochlorophyll Model Compound Containing trans-Dialkyl Substituents in Ring D," Chau Nguyen, K.; Wang, P.; Sommer, R. D.; Lindsey, J. S. J. Org. Chem. 2020, 85, 6605–6619. DOI: 10.1021/acs.joc.0c00608
Deposition Number: 1902485
Database Identifier: GUKDAU
388. "Chromogenic agents built around a multifunctional double-triazine framework for enzymatically triggered cross-linking under physiological conditions," Fujita, H.; Zhang, Y.; Wu, Z.; Lindsey, J. S. New J. Chem. 2020, 44, 3856–3867. DOI: 10.1039/C9NJ06187H
Deposition Number: 1958437
Database Identifier: SUHPET
387. "Use of the Nascent Isocyclic Ring to Anchor Assembly of the Full Skeleton of Model Chlorophylls,” Wang, P.; Lu, F.; Lindsey, J. S. J. Org. Chem. 2020, 85, 702–715. DOI: 10.1021/acs.joc.9b02770
Deposition Number: 1958436
Database Identifier: SUHPAP
387. "Use of the Nascent Isocyclic Ring to Anchor Assembly of the Full Skeleton of Model Chlorophylls,” Wang, P.; Lu, F.; Lindsey, J. S. J. Org. Chem. 2020, 85, 702–715. DOI: 10.1021/acs.joc.9b02770
Deposition Number: 1958435
Database Identifier: SUHNUH
387. "Use of the Nascent Isocyclic Ring to Anchor Assembly of the Full Skeleton of Model Chlorophylls,” Wang, P.; Lu, F.; Lindsey, J. S. J. Org. Chem. 2020, 85, 702–715. DOI: 10.1021/acs.joc.9b02770
Deposition Number: 1902488
Database Identifier: ROWKUM
386. “Enzymatically triggered chromogenic cross-linking agents under physiological conditions,” Fujita, H.; Dou, J.; Matsumoto, N.; Wu, Z.; Lindsey, J. S. New J. Chem. 2020, 44, 719–743. DOI: 10.1039/C9NJ04126E
Deposition Number: 1902489
Database Identifier: ROWLAT
386. “Enzymatically triggered chromogenic cross-linking agents under physiological conditions,” Fujita, H.; Dou, J.; Matsumoto, N.; Wu, Z.; Lindsey, J. S. New J. Chem. 2020, 44, 719–743. DOI: 10.1039/C9NJ04126E