2020–2021

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