Lash TD - Search Results

1

Grabowski EY, AbuSalim DI, Lash TD. Grabowski EY, et al. Among authors: lash td. J Org Chem. 2018 Oct 5;83(19):11825-11838. doi: 10.1021/acs.joc.8b01748. Epub 2018 Sep 11. J Org Chem. 2018. PMID: 30168327

2

Porphyrins with exocyclic rings. 14. Synthesis of tetraacenaphthoporphyrins, a new family of highly conjugated porphyrins with record-breaking long-wavelength electronic absorptions.

Spence JD, Lash TD. Spence JD, et al. Among authors: lash td. J Org Chem. 2000 Mar 10;65(5):1530-9. doi: 10.1021/jo991730w. J Org Chem. 2000. PMID: 10814118

3

Porphyrins with exocyclic rings. 15.(1) synthesis of quino- and isoquinoporphyrins, aza analogues of the naphthoporphyrins.

Lash TD, Gandhi V. Lash TD, et al. J Org Chem. 2000 Nov 17;65(23):8020-6. doi: 10.1021/jo001216m. J Org Chem. 2000. PMID: 11073612

4

Porphyrins with exocyclic rings. 16. Synthesis and spectroscopic characterization of fluoranthoporphyrins, a new class of highly conjugated porphyrin chromophores.

Lash TD, Werner TM, Thompson ML, Manley JM. Lash TD, et al. J Org Chem. 2001 May 4;66(9):3152-9. doi: 10.1021/jo010066s. J Org Chem. 2001. PMID: 11325282

5

Calix[4]azulene.

Colby DA, Lash TD. Colby DA, et al. Among authors: lash td. J Org Chem. 2002 Feb 8;67(3):1031-3. doi: 10.1021/jo0110101. J Org Chem. 2002. PMID: 11856059

6

Conjugated macrocycles related to the porphyrins. 21. Synthesis, spectroscopy, electrochemistry, and structural characterization of carbaporphyrins.

Lash TD, Hayes MJ, Spence JD, Muckey MA, Ferrence GM, Szczepura LF. Lash TD, et al. J Org Chem. 2002 Jul 12;67(14):4860-74. doi: 10.1021/jo020267b. J Org Chem. 2002. PMID: 12098299

7

Silver(III) carbaporphyrins: the first organometallic complexes of true carbaporphyrins.

Muckey MA, Szczepura LF, Ferrence GM, Lash TD. Muckey MA, et al. Among authors: lash td. Inorg Chem. 2002 Sep 23;41(19):4840-2. doi: 10.1021/ic020285b. Inorg Chem. 2002. PMID: 12230385

8

Conjugated macrocycles related to the porphyrins. 25. Proton NMR spectroscopic evidence for a preferred [18]annulene substructure in carbaporphyrins from the magnitude of selected 4J(H,H) CH=C-CH3 coupling constants.

Liu D, Lash TD. Liu D, et al. Among authors: lash td. J Org Chem. 2003 Mar 7;68(5):1755-61. doi: 10.1021/jo020703u. J Org Chem. 2003. PMID: 12608788

9

Tert-butyl-substituted tripyrranes: insights into the steric and conformational factors that influence porphyrinoid ring formation in the "3 + 1" methodology.

Jiao W, Lash TD. Jiao W, et al. Among authors: lash td. J Org Chem. 2003 May 16;68(10):3896-901. doi: 10.1021/jo0207628. J Org Chem. 2003. PMID: 12737569

10

Regioselective oxidations of benzocarbaporphyrins with ferric chloride: a facile synthesis of bridged [18]annulene ketals with strong absorptions in the far red and an unexpected halogenation reaction at the interior carbon atom.

Lash TD, Muckey MA, Hayes MJ, Liu D, Spence JD, Ferrence GM. Lash TD, et al. J Org Chem. 2003 Oct 31;68(22):8558-70. doi: 10.1021/jo030127h. J Org Chem. 2003. PMID: 14575486

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