Year |
Citation |
Score |
2023 |
Mathius MA, Chhoeun JM, Kaufman RH, AbuSalim DI, Lash TD. Linear Extension of Carbaporphyrin Chromophores: Synthesis, Protonation, and Metalation of Anthro[2,3-]carbaporphyrins: Evidence for 30π-Electron Aromatic Circuits in a Palladium(II) Complex. The Journal of Organic Chemistry. PMID 38110335 DOI: 10.1021/acs.joc.3c01839 |
0.427 |
|
2022 |
Lash TD, Mathius MA, AbuSalim DI. Synthesis of Chrysoporphyrins and a Related Benzopyrene-Fused System. The Journal of Organic Chemistry. 87: 16276-16296. PMID 36459435 DOI: 10.1021/acs.joc.2c01859 |
0.392 |
|
2022 |
Cramer EK, AbuSalim DI, Lash TD. Oxyquinoliziniporphyrins: Introduction of a Heterocyclic Dimension to Carbaporphyrinoid Systems. Organic Letters. PMID 35848058 DOI: 10.1021/acs.orglett.2c02098 |
0.364 |
|
2022 |
Cramer EK, Lash TD. Synthesis of a Series of Tropone-Fused Porphyrinoids. The Journal of Organic Chemistry. 87: 952-962. PMID 35018780 DOI: 10.1021/acs.joc.1c02063 |
0.387 |
|
2021 |
Lash TD, AbuSalim DI, Ferrence GM. Telluracarbaporphyrins and a Related Palladium(II) Complex: Evidence for Hypervalent Interactions. Inorganic Chemistry. 60: 9833-9847. PMID 34134482 DOI: 10.1021/acs.inorgchem.1c01039 |
0.661 |
|
2020 |
Latham AN, Lash TD. Synthesis and Characterization of N-Methylporphyrins, Heteroporphyrins, Carbaporphyrins and Related Systems. The Journal of Organic Chemistry. PMID 32940469 DOI: 10.1021/Acs.Joc.0C01737 |
0.381 |
|
2020 |
Almejbel AS, Lash TD. Synthesis of 2-bromo- and 2-phenyl-neo-confused porphyrins. Organic & Biomolecular Chemistry. PMID 32914153 DOI: 10.1039/D0Ob01642J |
0.564 |
|
2020 |
Moriones JSD, Latham AN, Lash TD. Synthesis of internally alkylated azuliporphyrins Journal of Porphyrins and Phthalocyanines. 24: 817-829. DOI: 10.1142/S1088424619501876 |
0.413 |
|
2020 |
Lash TD, Rooney JM. Alkylation, metalation and ring contraction of tropiporphyrin Journal of Porphyrins and Phthalocyanines. 24: 181-190. DOI: 10.1142/S1088424619501098 |
0.341 |
|
2019 |
Lash TD, Stateman LM, AbuSalim DI. Synthesis of Azulitriphyrins(1.2.1) and Related Benzocarbatriphyrins. The Journal of Organic Chemistry. PMID 31608646 DOI: 10.1021/Acs.Joc.9B02315 |
0.467 |
|
2019 |
Noboa MA, AbuSalim DI, Lash TD. Azulichlorins and Benzocarbachlorins Derived Therefrom. The Journal of Organic Chemistry. PMID 31429281 DOI: 10.1021/Acs.Joc.9B01578 |
0.465 |
|
2019 |
Jain P, AbuSalim DI, Lash TD. adj-Dicarbaporphyrinoid Systems: Synthesis, Spectroscopic Characterization and Reactivity of 23-Carbabenziporphyrins. The Journal of Organic Chemistry. PMID 31331169 DOI: 10.1021/Acs.Joc.9B01410 |
0.529 |
|
2019 |
Lash TD, Darrow WT, Latham AN, Sahota N, Ferrence GM. Rhodium Complexes of Carbaporphyrins, Carbachlorins, adj-Dicarbaporphyrins, and an adj-Dicarbachlorin. Inorganic Chemistry. PMID 31088085 DOI: 10.1021/Acs.Inorgchem.9B00721 |
0.682 |
|
2019 |
Latham AN, Ferrence GM, Lash TD. Metalation and Methyl Group Migration in 21-, 22-, and 23-Methylcarbaporphyrins: Synthesis and Characterization of Palladium(II), Rhodium(I), and Rhodium(III) Derivatives Organometallics. 38: 575-585. DOI: 10.1021/Acs.Organomet.8B00863 |
0.7 |
|
2018 |
AbuSalim DI, Lash TD. Tropylium and Porphyrinoid Character in Carbaporphyrinoid Systems. Relative Stability and Aromatic Characteristics of Azuliporphyrin and Tropiporphyrin Tautomers, Protonated Species, and Related Structures. The Journal of Physical Chemistry. A. PMID 30512952 DOI: 10.1021/Acs.Jpca.8B10020 |
0.406 |
|
2018 |
Lash TD, Fosu SC, Smolczyk TJ, AbuSalim DI. Synthesis of Expanded Porphyrinoids with Azulene and Indene Subunits and an opp-Dioxadicarbaporphyrin from Fulvene Carbinols and a Dioxacarbatripyrrin. The Journal of Organic Chemistry. PMID 30247904 DOI: 10.1021/Acs.Joc.8B01929 |
0.461 |
|
2018 |
Grabowski EY, AbuSalim DI, Lash TD. Naphtho[2,3- b]carbaporphyrins. The Journal of Organic Chemistry. PMID 30168327 DOI: 10.1021/Acs.Joc.8B01748 |
0.543 |
|
2018 |
Smolczyk TJ, Lash TD. Alphabet soup within a porphyrinoid cavity: synthesis of heterocarbaporphyrins with CNNO, CNOO, CNSO and CNSeO Cores from an oxacarbatripyrrin. Chemical Communications (Cambridge, England). PMID 30059085 DOI: 10.1039/C8Cc04976A |
0.439 |
|
2017 |
Lash TD, Ferrence GM. Metalation and Selective Oxidation of Diphenyl-23-oxa-, -thia-, and -selena-21-carbaporphyrins. Inorganic Chemistry. PMID 28872863 DOI: 10.1021/Acs.Inorgchem.7B01946 |
0.719 |
|
2017 |
Sahota N, Ferrence GM, Lash TD. Synthesis and properties of carbaporphyrin and carbachlorin dimethyl esters derived from cyclopentanedialdehydes. The Journal of Organic Chemistry. PMID 28849655 DOI: 10.1021/Acs.Joc.7B01831 |
0.745 |
|
2017 |
Gao R, Lash TD, AbuSalim DI. Pyreniporphyrins, porphyrin analogues that incorporate a polycyclic aromatic hydrocarbon subunit within the macrocyclic framework. The Journal of Organic Chemistry. PMID 28574261 DOI: 10.1021/Acs.Joc.7B00829 |
0.556 |
|
2017 |
Pokharel K, Ferrence GM, Lash TD. Late transition metal complexes of oxypyriporphyrin and the platinum(II) complex of oxybenziporphyrin Journal of Porphyrins and Phthalocyanines. 21: 493-501. DOI: 10.1142/S1088424617500535 |
0.68 |
|
2017 |
Darrow WT, Lash TD. An alternative synthesis of benziporphyrins starting from isophthaloyl chloride Journal of Porphyrins and Phthalocyanines. 21: 532-538. DOI: 10.1142/S1088424617500493 |
0.471 |
|
2017 |
Li D, Lash TD. Synthesis and Oxidation of Internally Chlorinated Carbachlorins European Journal of Organic Chemistry. 2017: 6775-6780. DOI: 10.1002/Ejoc.201701257 |
0.432 |
|
2016 |
Adiraju VA, Ferrence GM, Lash TD. Regioselective oxidation and metalation of meso-unsubstituted azuliporphyrins. Organic & Biomolecular Chemistry. 14: 10523-10533. PMID 27775128 DOI: 10.1039/C6Ob02052F |
0.718 |
|
2016 |
Lash TD. Carbaporphyrinoid Systems. Chemical Reviews. PMID 27657332 DOI: 10.1021/acs.chemrev.6b00326 |
0.385 |
|
2016 |
Adiraju VA, Ferrence GM, Lash TD. Rhodium(i), rhodium(iii) and iridium(iii) carbaporphyrins. Dalton Transactions (Cambridge, England : 2003). 45: 13691-4. PMID 27529466 DOI: 10.1039/C6Dt03093A |
0.698 |
|
2016 |
Lash TD. Out of the Blue! Azuliporphyrins and Related Carbaporphyrinoid Systems. Accounts of Chemical Research. 49: 471-82. PMID 26853353 DOI: 10.1021/Acs.Accounts.5B00523 |
0.444 |
|
2016 |
Lash TD. What’s in a name? The MacDonald condensation Journal of Porphyrins and Phthalocyanines. 20: 855-888. DOI: 10.1142/S1088424616300147 |
0.463 |
|
2016 |
Georghiou PE, Schneider C, Shamov G, Lash TD, Rahman S, Sabrina Giddings D. Mechanochemical formation of a 1:1 C 60: Tert -butylcalix[4]azulene supramolecular complex: Solid-state NMR and DFT computational studies Supramolecular Chemistry. 28: 396-402. DOI: 10.1080/10610278.2015.1108416 |
0.331 |
|
2015 |
AbuSalim DI, Lash TD. In Pursuit of Novel Porphyrin Isomers. Aromatic Character and Relative Stability of Conjugated Tetrapyrroles with Two Neo-Confused Rings or with Mixed Neo-Confused and N-Confused Subunits. The Journal of Physical Chemistry. A. 119: 11440-53. PMID 26509278 DOI: 10.1021/Acs.Jpca.5B08682 |
0.379 |
|
2015 |
Lash TD, AbuSalim DI, Ferrence GM. adj-Dicarbachlorin, the first free base carbaporphyrinoid system with an internal methylene unit. Chemical Communications (Cambridge, England). 51: 15952-5. PMID 26376706 DOI: 10.1039/C5Cc06890H |
0.618 |
|
2015 |
Stateman LM, Lash TD. Syntheses of Carbaporphyrinoid Systems Using a Carbatripyrrin Methodology. Organic Letters. 17: 4522-5. PMID 26327564 DOI: 10.1021/Acs.Orglett.5B02219 |
0.461 |
|
2015 |
Lash TD, Colby DA, El-Beck JA, AbuSalim DI, Ferrence GM. Preparation, Structural Characterization, Assessment of Potential Antiaromaticity and Metalation of 21-Oxyazuliporphyrins. Inorganic Chemistry. 54: 9174-87. PMID 26325126 DOI: 10.1021/Acs.Inorgchem.5B01587 |
0.711 |
|
2015 |
Celis AI, Streit BR, Moraski GC, Kant R, Lash TD, Lukat-Rodgers GS, Rodgers KR, DuBois JL. Unusual Peroxide-Dependent, Heme-Transforming Reaction Catalyzed by HemQ. Biochemistry. PMID 26083961 DOI: 10.1021/Acs.Biochem.5B00492 |
0.444 |
|
2015 |
Lash TD. Benziporphyrins, a unique platform for exploring the aromatic characteristics of porphyrinoid systems. Organic & Biomolecular Chemistry. 13: 7846-78. PMID 26061097 DOI: 10.1039/C5Ob00892A |
0.329 |
|
2015 |
Stateman LM, Ferrence GM, Lash TD. Rhodium(III) Azuliporphyrins Organometallics. 34: 3842-3848. DOI: 10.1021/Acs.Organomet.5B00433 |
0.699 |
|
2014 |
Fosu SC, Ferrence GM, Lash TD. Synthesis and metalation of dimethoxybenziporphyrins, thiabenziporphyrins, and dibenziporphyrins. The Journal of Organic Chemistry. 79: 11061-74. PMID 25321316 DOI: 10.1021/Jo502063W |
0.745 |
|
2014 |
AbuSalim DI, Lash TD. Relative stability of benziporphyrin and naphthiporphyrin tautomers and the emergence of macrocyclic diatropicity. Organic & Biomolecular Chemistry. 12: 8719-36. PMID 25257815 DOI: 10.1039/C4Ob01659A |
0.397 |
|
2014 |
Lash TD, Gilot GC, AbuSalim DI. Tropone-fused carbaporphyrins. The Journal of Organic Chemistry. 79: 9704-16. PMID 25229306 DOI: 10.1021/Jo5018553 |
0.528 |
|
2014 |
Li D, Lash TD. Synthesis and reactivity of carbachlorins and carbaporphyrins. The Journal of Organic Chemistry. 79: 7112-21. PMID 25000116 DOI: 10.1021/Jo501287Q |
0.544 |
|
2014 |
AbuSalim DI, Ferrence GM, Lash TD. Synthesis of an adj-dicarbaporphyrin and the formation of an unprecedented tripalladium sandwich complex. Journal of the American Chemical Society. 136: 6763-72. PMID 24738618 DOI: 10.1021/Ja502795X |
0.71 |
|
2014 |
Li R, Lammer AD, Ferrence GM, Lash TD. Synthesis, structural characterization, aromatic characteristics, and metalation of neo-confused porphyrins, a newly discovered class of porphyrin isomers. The Journal of Organic Chemistry. 79: 4078-93. PMID 24697282 DOI: 10.1021/Jo500580E |
0.745 |
|
2014 |
Lash TD. Metal complexes of carbaporphyrinoid systems. Chemistry, An Asian Journal. 9: 682-705. PMID 24482394 DOI: 10.1002/Asia.201301594 |
0.33 |
|
2014 |
Lash TD, El-Beck JA, Ferrence GM. Synthesis, structural characterization and reactivity of heteroazuliporphyrins. Organic & Biomolecular Chemistry. 12: 316-29. PMID 24253355 DOI: 10.1039/C3Ob41992D |
0.711 |
|
2013 |
AbuSalim DI, Lash TD. Aromatic character and relative stability of neo-confused porphyrin tautomers and related compounds. Organic & Biomolecular Chemistry. 11: 8306-23. PMID 24201817 DOI: 10.1039/C3Ob42063A |
0.343 |
|
2013 |
AbuSalim DI, Lash TD. Relative stability and diatropic character of carbaporphyrin, dicarbaporphyrin, tricarbaporphyrin, and quatyrin tautomers. The Journal of Organic Chemistry. 78: 11535-48. PMID 24188188 DOI: 10.1021/Jo4021198 |
0.335 |
|
2013 |
Young AM, Lash TD. 6-Oxopyriphlorins. Organic & Biomolecular Chemistry. 11: 6841-8. PMID 24175332 DOI: 10.1039/c3ob41506f |
0.411 |
|
2013 |
AbuSalim DI, Merfeld ML, Lash TD. Dicarbaporphyrinoid systems. Synthesis of oxo-adj-dibenziphlorins. The Journal of Organic Chemistry. 78: 10360-8. PMID 24063344 DOI: 10.1021/Jo401756Q |
0.452 |
|
2013 |
Lash TD, Toney AM, Castans KM, Ferrence GM. Synthesis of benziporphyrins and heterobenziporphyrins and an assessment of the diatropic characteristics of the protonated species. The Journal of Organic Chemistry. 78: 9143-52. PMID 23944643 DOI: 10.1021/Jo401365P |
0.744 |
|
2013 |
Li R, Ferrence GM, Lash TD. Synthesis of a neo-confused porphyrin and an unusual dihydroporphyrin derivative. Chemical Communications (Cambridge, England). 49: 7537-9. PMID 23868015 DOI: 10.1039/C3Cc44248A |
0.688 |
|
2012 |
Lash TD, Pokharel K, Zeller M, Ferrence GM. Iridium(III) azuliporphyrins. Chemical Communications (Cambridge, England). 48: 11793-5. PMID 23111425 DOI: 10.1039/C2Cc37104A |
0.666 |
|
2012 |
Lash TD, Bergman KM. Further observations on conformational and substituent effects in acid-catalyzed "3 + 1" cyclizations of tripyrranes with aromatic dialdehydes. The Journal of Organic Chemistry. 77: 9774-83. PMID 23030771 DOI: 10.1021/Jo301945F |
0.518 |
|
2012 |
Lash TD, Lammer AD, Ferrence GM. Two-step synthesis of stable dioxadicarbaporphyrins from bis(3-indenyl)methane. Angewandte Chemie (International Ed. in English). 51: 10871-5. PMID 23001702 DOI: 10.1002/Anie.201206385 |
0.652 |
|
2012 |
Lash TD, Lammer AD, Idate AS, Colby DA, White K. Preparation of azulene-derived fulvenedialdehydes and their application to the synthesis of stable adj-dicarbaporphyrinoids. The Journal of Organic Chemistry. 77: 2368-81. PMID 22288783 DOI: 10.1021/Jo2026977 |
0.5 |
|
2012 |
Lash TD. Carbaporphyrins, porphyrin isomers and the legacy of Emanuel Vogel Journal of Porphyrins and Phthalocyanines. 16: 423-433. DOI: 10.1142/S1088424612300017 |
0.44 |
|
2011 |
Lash TD, Lammer AD, Ferrence GM. Neo-confused porphyrins, a new class of porphyrin isomers. Angewandte Chemie (International Ed. in English). 50: 9718-21. PMID 21948730 DOI: 10.1002/Anie.201104826 |
0.597 |
|
2011 |
Lash TD. Unexpected alkyl group migration in palladium(II) benzocarbaporphyrins. Organic Letters. 13: 4632-5. PMID 21812402 DOI: 10.1021/Ol2018483 |
0.463 |
|
2011 |
Young AM, Von Ruden AL, Lash TD. Pyrazole analogues of porphyrins and oxophlorins. Organic & Biomolecular Chemistry. 9: 6293-305. PMID 21792456 DOI: 10.1039/C1Ob05603D |
0.543 |
|
2011 |
Taylor VM, Cedeño DL, Muñoz DL, Jones MA, Lash TD, Young AM, Constantino MH, Esposito N, Vélez ID, Robledo SM. In vitro and in vivo studies of the utility of dimethyl and diethyl carbaporphyrin ketals in treatment of cutaneous leishmaniasis. Antimicrobial Agents and Chemotherapy. 55: 4755-64. PMID 21788471 DOI: 10.1128/Aac.00671-11 |
0.307 |
|
2011 |
Lash TD, Miyake K, Xu L, Ferrence GM. Synthesis of a series of aromatic benziporphyrins and heteroanalogues via tripyrrane-like intermediates derived from resorcinol and 2-methylresorcinol. The Journal of Organic Chemistry. 76: 6295-308. PMID 21692522 DOI: 10.1021/Jo201098C |
0.735 |
|
2011 |
Lash TD, Young AM, Rasmussen JM, Ferrence GM. Naphthiporphyrins. The Journal of Organic Chemistry. 76: 5636-51. PMID 21604773 DOI: 10.1021/jo200622s |
0.719 |
|
2011 |
Lash TD, Smith BE, Melquist MJ, Godfrey BA. Synthesis of indenoporphyrins, highly modified porphyrins with reduced diatropic characteristics. The Journal of Organic Chemistry. 76: 5335-45. PMID 21598988 DOI: 10.1021/Jo2006895 |
0.477 |
|
2011 |
Lash TD, Lamm TR, Schaber JA, Chung WH, Johnson EK, Jones MA. Normal and abnormal heme biosynthesis. Part 7. Synthesis and metabolism of coproporphyrinogen-III analogues with acetate or butyrate side chains on rings C and D. Development of a modified model for the active site of coproporphyrinogen oxidase. Bioorganic & Medicinal Chemistry. 19: 1492-504. PMID 21277781 DOI: 10.1016/J.Bmc.2010.12.053 |
0.413 |
|
2011 |
Lash TD. Origin of aromatic character in porphyrinoid systems Journal of Porphyrins and Phthalocyanines. 15: 1093-1115. DOI: 10.1142/S1088424611004063 |
0.344 |
|
2010 |
Jain P, Ferrence GM, Lash TD. Preparation of furan and thiophene-derived fulvene dialdehydes: synthesis and structural characterization of a 22-oxa-21-carbaporphyrin and a related palladium(II) organometallic complex. The Journal of Organic Chemistry. 75: 6563-73. PMID 20828115 DOI: 10.1021/Jo101310M |
0.74 |
|
2010 |
Lash TD, Jones SA, Ferrence GM. Synthesis and characterization of tetraphenyl-21,23-dideazaporphyrin: the best evidence yet that porphyrins really are the [18]annulenes of nature. Journal of the American Chemical Society. 132: 12786-7. PMID 20795621 DOI: 10.1021/Ja105146A |
0.663 |
|
2010 |
Lash TD, Mani UN, Keck AS, Jones MA. Normal and abnormal heme biosynthesis. 6. Synthesis and metabolism of a series of monovinylporphyrinogens related to harderoporphyrinogen. Further insights into the oxidative decarboxylation of porphyrinogen substrates by coproporphyrinogen oxidase. The Journal of Organic Chemistry. 75: 3183-92. PMID 20387847 DOI: 10.1021/Jo100083T |
0.386 |
|
2010 |
Boedigheimer H, Ferrence GM, Lash TD. Porphyrin on a half-shell! Synthesis and characterization of corannulenoporphyrins. The Journal of Organic Chemistry. 75: 2518-27. PMID 20297807 DOI: 10.1021/Jo902592U |
0.744 |
|
2010 |
Smith BE, Lash TD. Porphyrins with exocyclic rings. Part 25: synthesis of porphyrins with a fused cyclic ether subunit from tetrahydro-4H-pyan-4-one Tetrahedron. 66: 4413-4422. DOI: 10.1016/J.Tet.2010.04.069 |
0.531 |
|
2010 |
Gandhi V, Thompson ML, Lash TD. Porphyrins with exocyclic rings. Part 24. Synthesis and spectroscopic properties of pyrenoporphyrins, potential building blocks for porphyrin molecular wires Tetrahedron. 66: 1787-1799. DOI: 10.1016/J.Tet.2010.01.046 |
0.497 |
|
2010 |
Graham SR, Ferrence GM, Lash TD. ChemInform Abstract: Conjugated Macrocycles Related to the Porphyrins. Part 20. Organometallic Chemistry of Carbaporphyrinoids: Synthesis and Characterization of Nickel(II) and Palladium(II) Azuliporphyrins. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200227153 |
0.648 |
|
2010 |
Lash TD, Werner TM, Thompson ML, Manley JM. ChemInform Abstract: Porphyrins with Exocyclic Rings. Part 16. Synthesis and Spectroscopic Characterization of Fluoranthoporphyrins, a New Class of Highly Conjugated Porphyrin Chromophores. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200137123 |
0.372 |
|
2010 |
Lash TD, Romanic JL, Hayes MJ, Spence JD. ChemInform Abstract: Conjugated Macrocycles Related to the Porphyrins. Part 15. Towards Hydrocarbon Analogues of the Porphyrins: Synthesis and Spectroscopic Characterization of the First Dicarbaporphyrin. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199934138 |
0.373 |
|
2010 |
NOVAK BH, LASH TD. ChemInform Abstract: Porphyrins with Exocyclic Rings. Part 11. Synthesis and Characterization of Phenanthroporphyrins, a New Class of Modified Porphyrin Chromophores. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199844117 |
0.348 |
|
2010 |
LASH TD, CHANEY ST. ChemInform Abstract: Conjugated Macrocycles Related to the Porphyrins. Part 6. Oxypyriporphyrin, the First Fully Aromatic Porphyrinoid Macrocycle with a Pyridine Subunit. Cheminform. 27: no-no. DOI: 10.1002/chin.199646121 |
0.31 |
|
2010 |
LASH TD. ChemInform Abstract: Synthesis of Porphyrins with Exocyclic Rings from Cycloalkenopyrroles Cheminform. 26: no-no. DOI: 10.1002/chin.199539294 |
0.335 |
|
2010 |
LASH TD, BLADEL KA, SHINER CM, ZAJESKI DL, BALASUBRAMANIAM RP. ChemInform Abstract: Porphyrins with Exocyclic Rings. Part 1. Chemistry of 4,5,6,7- Tetrahydro-1H-indoles: Synthesis of Acetoxy Derivatives, Dihydroindoles, and Novel Porphyrins with Four Exocyclic Rings. Cheminform. 24: no-no. DOI: 10.1002/chin.199305253 |
0.344 |
|
2010 |
LASH TD. ChemInform Abstract: Conjugated Macrocycles Related to the Porphyrins. Part 4. Synthesis of a 23,24-Dioxa-5-oxophlorin (III). Cheminform. 23: no-no. DOI: 10.1002/chin.199250234 |
0.355 |
|
2009 |
Lash TD, El-Beck JA, Colby DA. Synthesis of a tetraazulene porphodimethene analogue. The Journal of Organic Chemistry. 74: 8830-3. PMID 19908914 DOI: 10.1021/Jo901959K |
0.432 |
|
2009 |
Zhang Z, Ferrence GM, Lash TD. MacDonald-type reactions using bis-acrylaldehydes: synthesis of an expanded sapphyrin and vinylogous hexaphyrins. Organic Letters. 11: 1249-52. PMID 19245245 DOI: 10.1021/Ol802945S |
0.678 |
|
2009 |
Zhang Z, Ferrence GM, Lash TD. adj-Diazuliporphyrins, a new family of dicarbaporphyrinoids with unprecedented mesoionic characteristics. Organic Letters. 11: 101-4. PMID 19049407 DOI: 10.1021/Ol802406F |
0.67 |
|
2009 |
Davis RN, Lash TD. Preparation of stable fulvene and difulvene aldehydes from benzaldehydes and an indene-derived enamine: formation of novel indene-fused benzodiazepines and attempted syntheses of di- and tricarbaporphyrinoid systems Tetrahedron. 65: 9935-9943. DOI: 10.1016/J.Tet.2009.10.013 |
0.497 |
|
2009 |
Lash TD, Yant VR. Improved syntheses of meso-tetraarylbenziporphyrins and observations of substituent effects on the diatropic characteristics of these formally nonaromatic carbaporphyrinoids Tetrahedron. 65: 9527-9535. DOI: 10.1016/J.Tet.2009.09.060 |
0.544 |
|
2008 |
Lash TD, Young AM, Von Ruden AL, Ferrence GM. Adding to the confusion! Synthesis and metalation of pyrazole analogues of the porphyrins. Chemical Communications (Cambridge, England). 6309-11. PMID 19048138 DOI: 10.1039/B816057K |
0.645 |
|
2008 |
Lash TD, Von Ruden AL. Synthesis and reactivity of N-methyl and N-phenyl meso-unsubstituted N-confused porphyrins. The Journal of Organic Chemistry. 73: 9417-25. PMID 18991377 DOI: 10.1021/Jo802040Q |
0.53 |
|
2007 |
Lash TD, Colby DA, Idate AS, Davis RN. Fulvene dialdehyde strategy for adj-dicarbaporphyrinoid synthesis: preparation of a 22-carbaazuliporphyrin. Journal of the American Chemical Society. 129: 13800-1. PMID 17944474 DOI: 10.1021/Ja076414A |
0.478 |
|
2007 |
Lash TD, El-Beck JA, Ferrence GM. Syntheses and reactivity of meso-unsubstituted azuliporphyrins derived from 6-tert-butyl- and 6-phenylazulene. The Journal of Organic Chemistry. 72: 8402-15. PMID 17918898 DOI: 10.1021/Jo701523S |
0.747 |
|
2007 |
Lash TD, Szymanski JT, Ferrence GM. Tetraaryldimethoxybenziporphyrins. At the edge of carbaporphyrinoid aromaticity. The Journal of Organic Chemistry. 72: 6481-92. PMID 17655255 DOI: 10.1021/Jo070947K |
0.727 |
|
2007 |
Lash TD, Pokharel K, Serling JM, Yant VR, Ferrence GM. Aromatic and nonaromatic pyriporphyrins. Organic Letters. 9: 2863-6. PMID 17602489 DOI: 10.1021/Ol071052X |
0.677 |
|
2007 |
Stephenson JR, Stacey JA, Morgenthaler JB, Friesen JA, Lash TD, Jones MA. Role of aspartate 400, arginine 262, and arginine 401 in the catalytic mechanism of human coproporphyrinogen oxidase. Protein Science : a Publication of the Protein Society. 16: 401-10. PMID 17242372 DOI: 10.1110/Ps.062636907 |
0.328 |
|
2007 |
Ferrence GM, Lash TD. (23-tert-Butyl-5,10,15,20-tetraphenylazuliporphyrinato)palladium(II) dichloromethane solvate Acta Crystallographica Section E Structure Reports Online. 63: m1351-m1353. DOI: 10.1107/S1600536807015528 |
0.626 |
|
2007 |
Lash TD, Marron TG, Bastian JA. Porphyrins with exocyclic rings. Part 23: Synthesis of porphyrins with large exocyclic rings—cyclohexadeca[b]pyrroles and porphyrins therefrom Tetrahedron. 63: 12343-12351. DOI: 10.1016/J.Tet.2007.09.060 |
0.494 |
|
2007 |
Lash TD, Li W, Quizon-Colquitt DM. Porphyrins with exocyclic rings. Part 22: Synthesis of deoxophylloerythroetioporphyrin (DPEP), three ring homologues, and five related nonpolar bacteriopetroporphyrins using a western ring closure and an improved b-bilene methodology Tetrahedron. 63: 12324-12342. DOI: 10.1016/J.Tet.2007.09.059 |
0.47 |
|
2007 |
El-Beck JA, Lash TD. Synthesis and Reactivity of 23-tert-Butyl- and 23-Phenyltetraarylazuliporphyrins: an Analysis of the Effect of Bulky Substituents on Oxidative Ring Contractions to Benzocarbaporphyrins (Eur. J. Org. Chem. 24/2007) European Journal of Organic Chemistry. 2007: 3953-3953. DOI: 10.1002/Ejoc.200790057 |
0.417 |
|
2007 |
El-Beck JA, Lash TD. Synthesis and Reactivity of 23-tert-Butyl- and 23-Phenyltetraarylazuliporphyrins: an Analysis of the Effect of Bulky Substituents on Oxidative Ring Contractions to Benzocarbaporphyrins European Journal of Organic Chemistry. 2007: 3981-3990. DOI: 10.1002/Ejoc.200700526 |
0.541 |
|
2007 |
Lash TD. Recent Advances on the Synthesis and Chemistry of Carbaporphyrins and Related Porphyrinoid Systems European Journal of Organic Chemistry. 2007: 5461-5481. DOI: 10.1002/Ejoc.200700478 |
0.408 |
|
2007 |
Xu L, Ferrence GM, Lash TD. Conjugated Macrocycles Related to the Porphyrins. Part 39. [22]Porphyrin-(3.1.1.3), a New Vinylogous Expanded Porphyrin System. Cheminform. 38. DOI: 10.1002/CHIN.200705112 |
0.591 |
|
2006 |
El-Beck JA, Lash TD. Tetraphenyloxybenziporphyrin, a new organometallic ligand for silver(III) and gold(III). Organic Letters. 8: 5263-6. PMID 17078693 DOI: 10.1021/Ol062108A |
0.493 |
|
2006 |
Xu L, Ferrence GM, Lash TD. [22]Porphyrin-(3.1.1.3), a new vinylogous expanded porphyrin system. Organic Letters. 8: 5113-6. PMID 17048856 DOI: 10.1021/Ol062043B |
0.722 |
|
2006 |
Xu L, Lash TD. Synthesis of aromatic dicarbaporphyrinoids from resorcinol and 2-methylresorcinol Tetrahedron Letters. 47: 8863-8866. DOI: 10.1016/J.Tetlet.2006.10.053 |
0.442 |
|
2006 |
Shiner CM, Lash TD. Porphyrins with Exocyclic Rings. Part 21. Influence of Pyrrolic and Carbocyclic Ring Alkyl Substituents on the Synthesis of Porphyrins Bearing Six-Membered Exocyclic Rings. Cheminform. 37. DOI: 10.1016/J.Tet.2005.10.019 |
0.53 |
|
2006 |
Cillo CM, Lash TD. Porphyrins with Exocyclic Rings. Part 20. Synthesis and Spectroscopic Characterization of Porphyrins with Fused 2,1,3-Benzoxadiazole and 2,1,3-Benzoselenadiazole Moieties. Cheminform. 37. DOI: 10.1002/CHIN.200605102 |
0.392 |
|
2006 |
Lash TD, Lin Y, Novak BH, Parikh MD. Porphyrins with Exocyclic Rings. Part 19. Efficient Syntheses of Phenanthrolinoporphyrins. Cheminform. 37. DOI: 10.1002/CHIN.200605101 |
0.304 |
|
2005 |
Cooper CL, Stob CM, Jones MA, Lash TD. Metabolism of pentacarboxylate porphyrinogens by highly purified human coproporphyrinogen oxidase: further evidence for the existence of an abnormal pathway for heme biosynthesis. Bioorganic & Medicinal Chemistry. 13: 6244-51. PMID 16084099 DOI: 10.1016/J.Bmc.2005.06.051 |
0.336 |
|
2005 |
Lash TD. The enigma of coproporphyrinogen oxidase: how does this unusual enzyme carry out oxidative decarboxylations to afford vinyl groups? Bioorganic & Medicinal Chemistry Letters. 15: 4506-9. PMID 16061377 DOI: 10.1016/J.Bmcl.2005.07.010 |
0.303 |
|
2005 |
Manley JM, Roper TJ, Lash TD. Synthesis of isomeric angularly annealed dinaphthoporphyrin systems: examination of the relative positioning and orientation of ring fusion as factors influencing the porphyrin chromophore. The Journal of Organic Chemistry. 70: 874-91. PMID 15675845 DOI: 10.1021/Jo040269R |
0.454 |
|
2005 |
He J, Kaprak TA, Jones MA, Lash TD. Normal and abnormal heme biosynthesis Part 4: Molecular dynamics simulations of coproporphyrinogen-III and related di- and tricarboxylic acids Journal of Porphyrins and Phthalocyanines. 9: 170-185. DOI: 10.1142/S1088424605000241 |
0.326 |
|
2005 |
Lash TD, Chen S. Syntheses of per-15N labeled etioporphyrins I–IV and a related tetrahydrobenzoporphyrin for applications in organic geochemistry and vibrational spectroscopy Tetrahedron. 61: 11577-11600. DOI: 10.1016/J.Tet.2005.09.105 |
0.427 |
|
2005 |
Cillo CM, Lash TD. Porphyrins with exocyclic rings. Part 20: Synthesis and spectroscopic characterization of porphyrins with fused 2,1,3-benzoxadiazole and 2,1,3-benzoselenadiazole moieties Tetrahedron. 61: 11615-11627. DOI: 10.1016/J.Tet.2005.09.090 |
0.565 |
|
2005 |
Lash TD, Lin Y, Novak BH, Parikh MD. Porphyrins with exocyclic rings. Part 19: Efficient syntheses of phenanthrolinoporphyrins Tetrahedron. 61: 11601-11614. DOI: 10.1016/J.Tet.2005.09.089 |
0.501 |
|
2004 |
Lash TD, Colby DA, Graham SR, Chaney ST. Synthesis, spectroscopy, and reactivity of meso-unsubstituted azuliporphyrins and their heteroanalogues. Oxidative ring contractions to carba-, oxacarba-, thiacarba-, and selenacarbaporphyrins. The Journal of Organic Chemistry. 69: 8851-64. PMID 15575767 DOI: 10.1021/Jo0402531 |
0.51 |
|
2004 |
Richter DT, Lash TD. Synthesis of sapphyrins, heterosapphyrins, and carbasapphyrins by a "4 + 1" approach. The Journal of Organic Chemistry. 69: 8842-50. PMID 15575766 DOI: 10.1021/Jo040239O |
0.477 |
|
2004 |
Bergman KM, Ferrence GM, Lash TD. Tropiporphyrins, cycloheptatrienyl analogues of the porphyrins: synthesis, spectroscopy, chemistry, and structural characterization of a silver(III) derivative. The Journal of Organic Chemistry. 69: 7888-97. PMID 15527266 DOI: 10.1021/Jo040213X |
0.716 |
|
2004 |
Liu D, Ferrence GM, Lash TD. Oxybenziporphyrins, oxypyriporphyrins, benzocarbaporphyrins, and their 23-oxa and 23-thia analogues: synthesis, spectroscopic characterization, metalation, and structural characterization of a palladium(II) organometallic derivative. The Journal of Organic Chemistry. 69: 6079-93. PMID 15373493 DOI: 10.1021/Jo040180L |
0.75 |
|
2004 |
Colby DA, Ferrence GM, Lash TD. Oxidative metalation of azuliporphyrins with copper(II) salts: formation of a porphyrin analogue system with a unique fully conjugated nonaromatic azulene subunit. Angewandte Chemie (International Ed. in English). 43: 1346-9. PMID 15368402 DOI: 10.1002/Anie.200353189 |
0.648 |
|
2004 |
Lash TD, Colby DA, Szczepura LF. New riches in carbaporphyrin chemistry: silver and gold organometallic complexes of benzocarbaporphyrins. Inorganic Chemistry. 43: 5258-67. PMID 15310203 DOI: 10.1021/Ic0400540 |
0.503 |
|
2004 |
Lash TD, Rasmussen JM, Bergman KM, Colby DA. Carbaporphyrinoid chemistry has a silver lining! silver(III) oxybenzi-, oxynaphthi-, tropi-, and benzocarbaporphyrins. Organic Letters. 6: 549-52. PMID 14961620 DOI: 10.1021/Ol0363265 |
0.38 |
|
2004 |
Miyake K, Lash TD. Preparation of tripyrrane analogues from resorcinol and 2-methylresorcinol for applications in the synthesis of new benziporphyrin systems. Chemical Communications (Cambridge, England). 178-9. PMID 14737537 DOI: 10.1039/B313229N |
0.481 |
|
2004 |
Cillo CM, Lash TD. Benzo[1,2-c:3,4-c']bis[1,2,5]selenadiazole, [1,2,5]selenadiazolo-[3,4-e]-2,1,3-benzothiadiazole, furazanobenzo-2,1,3-thiadiazole, furazanobenzo-2,1,3-selenadiazole and related heterocyclic systems Journal of Heterocyclic Chemistry. 41: 955-962. DOI: 10.1002/Jhet.5570410616 |
0.308 |
|
2004 |
Zhang B, Lash TD. Total Synthesis of the Porphyrin Mineral Abelsonite and Related Petroporphyrins with Five-Membered Exocyclic Rings. Cheminform. 35. DOI: 10.1002/CHIN.200401096 |
0.304 |
|
2003 |
Lash TD, Colby DA, Graham SR, Ferrence GM, Szczepura LF. Organometallic chemistry of azuliporphyrins: synthesis, spectroscopy, electrochemistry, and structural characterization of nickel(II), palladium(II), and platinum(II) complexes of azuliporphyrins. Inorganic Chemistry. 42: 7326-38. PMID 14577805 DOI: 10.1021/Ic030166B |
0.701 |
|
2003 |
Lash TD, Muckey MA, Hayes MJ, Liu D, Spence JD, Ferrence GM. 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. The Journal of Organic Chemistry. 68: 8558-70. PMID 14575486 DOI: 10.1021/Jo030127H |
0.712 |
|
2003 |
Jiao W, Lash TD. Tert-butyl-substituted tripyrranes: insights into the steric and conformational factors that influence porphyrinoid ring formation in the "3 + 1" methodology. The Journal of Organic Chemistry. 68: 3896-901. PMID 12737569 DOI: 10.1021/Jo0207628 |
0.52 |
|
2003 |
Liu D, Lash TD. 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. The Journal of Organic Chemistry. 68: 1755-61. PMID 12608788 DOI: 10.1021/Jo020703U |
0.343 |
|
2003 |
Zhang B, Lash TD. Total synthesis of the porphyrin mineral abelsonite and related petroporphyrins with five-membered exocyclic rings Tetrahedron Letters. 44: 7253-7256. DOI: 10.1016/J.Tetlet.2003.08.007 |
0.429 |
|
2003 |
Lash TD, Colby DA, Ferrence GM. Further Studies on the Synthesis of meso-Tetraarylazuliporphyrins under Lindsey-Rothemund Reaction Conditions and Their Conversion into Benzocarbaporphyrins European Journal of Organic Chemistry. 4533-4548. DOI: 10.1002/Ejoc.200300530 |
0.718 |
|
2003 |
Jiao W, Lash TD. Conjugated Macrocycles Related to the Porphyrins. Part 26. tert-Butyl-Substituted Tripyrranes: Insights into the Steric and Conformational Factors that Influence Porphyrinoid Ring Formation in the [3 + 2] Methodology. Cheminform. 34. DOI: 10.1002/CHIN.200332081 |
0.314 |
|
2002 |
Graham SR, Colby DA, Lash TD. An azulene analogue of the tripyrranes and carbaporphyrinoids therefrom. Angewandte Chemie (International Ed. in English). 41: 1371-4. PMID 19750768 DOI: 10.1002/1521-3773(20020415)41:8<1371::Aid-Anie1371>3.0.Co;2-Q |
0.364 |
|
2002 |
Colby DA, Lash TD. Adaptation of the Rothemund reaction for carbaporphyrin synthesis: preparation of meso-tetraphenylazuliporphyrin and related benzocarbaporphyrins. Chemistry (Weinheim An Der Bergstrasse, Germany). 8: 5397-402. PMID 12561311 DOI: 10.1002/1521-3765(20021202)8:23<5397::Aid-Chem5397>3.0.Co;2-D |
0.467 |
|
2002 |
Liu D, Lash TD. Synthesis, spectroscopy and metallation of mixed carbaporphyrinoid systems. Chemical Communications (Cambridge, England). 2426-7. PMID 12430473 DOI: 10.1039/B206276N |
0.52 |
|
2002 |
Muckey MA, Szczepura LF, Ferrence GM, Lash TD. Silver(III) carbaporphyrins: the first organometallic complexes of true carbaporphyrins. Inorganic Chemistry. 41: 4840-2. PMID 12230385 DOI: 10.1021/Ic020285B |
0.694 |
|
2002 |
Graham SR, Ferrence GM, Lash TD. Organometallic chemistry of carbaporphyrinoids: synthesis and characterization of nickel(II) and palladium(II) azuliporphyrins. Chemical Communications (Cambridge, England). 894-5. PMID 12123032 DOI: 10.1039/B200131B |
0.696 |
|
2002 |
Lash TD, Hayes MJ, Spence JD, Muckey MA, Ferrence GM, Szczepura LF. Conjugated macrocycles related to the porphyrins. 21. Synthesis, spectroscopy, electrochemistry, and structural characterization of carbaporphyrins. The Journal of Organic Chemistry. 67: 4860-74. PMID 12098299 DOI: 10.1021/Jo020267B |
0.723 |
|
2002 |
Colby DA, Lash TD. Calix[4]azulene. The Journal of Organic Chemistry. 67: 1031-3. PMID 11856059 DOI: 10.1021/Jo0110101 |
0.421 |
|
2002 |
Jones MA, He J, Lash TD. Kinetic studies of novel di- and tri-propionate substrates for the chicken red blood cell enzyme coproporphyrinogen oxidase. Journal of Biochemistry. 131: 201-5. PMID 11820932 DOI: 10.1093/Oxfordjournals.Jbchem.A003088 |
0.314 |
|
2002 |
Boggess JM, Czernuszewicz RS, Lash TD. Fingerprinting petroporphyrin structures with vibrational spectroscopy. Part 6: resonance Raman characterization of regioisomers of nickel(II) benzoetioporphyrin Organic Geochemistry. 33: 1111-1126. DOI: 10.1016/S0146-6380(02)00055-4 |
0.361 |
|
2001 |
Stepień M, Latos-Grazyński L, Lash TD, Szterenberg L. Palladium (II) complexes of oxybenziporphyrin. Inorganic Chemistry. 40: 6892-900. PMID 11754269 DOI: 10.1021/Ic010394A |
0.401 |
|
2001 |
Lash TD, Hall T, Mani UN, Jones MA. Normal and abnormal heme biosynthesis. 3.(1)Synthesis and metabolism of tripropionate analogues of coproporphyrinogen-III: novel probes for the active site of coproporphyrinogen oxidase. The Journal of Organic Chemistry. 66: 3753-9. PMID 11374994 DOI: 10.1021/Jo001697+ |
0.384 |
|
2001 |
Lash TD, Werner TM, Thompson ML, Manley JM. Porphyrins with exocyclic rings. 16. Synthesis and spectroscopic characterization of fluoranthoporphyrins, a new class of highly conjugated porphyrin chromophores. The Journal of Organic Chemistry. 66: 3152-9. PMID 11325282 DOI: 10.1021/Jo010066S |
0.555 |
|
2001 |
Richter DT, Lash TD. Conjugated macrocycles related to the porphyrins. Part 18: Synthesis and spectroscopic characterization of electron-rich benzi- and oxybenziporphyrins: influence of steric and electronic factors on porphyrinoid aromaticity Tetrahedron. 57: 3657-3671. DOI: 10.1016/S0040-4020(01)00256-3 |
0.497 |
|
2001 |
LASH TD. Modification of the porphyrin chromophore by ring fusion: identifying trends due to annelation of the porphyrin nucleus Journal of Porphyrins and Phthalocyanines. 5: 267-288. DOI: 10.1002/Jpp.313 |
0.351 |
|
2000 |
Lash TD, Gandhi V. Porphyrins with exocyclic rings. 15. Synthesis of quino- and isoquinoporphyrins, aza analogues of the naphthoporphyrins Journal of Organic Chemistry. 65: 8020-8026. PMID 11073612 DOI: 10.1021/Jo001216M |
0.489 |
|
2000 |
Spence JD, Lash TD. Porphyrins with exocyclic rings. 14. Synthesis of tetraacenaphthoporphyrins, a new family of highly conjugated porphyrins with record-breaking long-wavelength electronic absorptions. The Journal of Organic Chemistry. 65: 1530-9. PMID 10814118 DOI: 10.1021/Jo991730W |
0.389 |
|
2000 |
Lash TD, Thompson ML, Werner TM, Spence JD. Synthesis of Novel Pyrrolic Compounds from Nitroarenes and Isocyanoacetates Using a Phosphazene Superbase Synlett. 2000: 213-216. DOI: 10.1055/S-2000-6504 |
0.363 |
|
2000 |
Burns DH, Shi DC, Lash TD. Synthesis of the chlorin macrocycle by the ‘3 + 1’ approach Chemical Communications. 299-300. DOI: 10.1039/A908784B |
0.422 |
|
1999 |
Schertz T, Lash TD, Petryka JC, Reiter RC, Stevenson CD. Ion Association Assisted Lithium Ion "Claw" The Journal of Organic Chemistry. 64: 1849-1852. PMID 11674273 DOI: 10.1021/Jo981672Z |
0.388 |
|
1999 |
Lash TD, Romanic JL, Hayes MJ, Spence JD. Towards hydrocarbon analogues of the porphyrins: synthesis and spectroscopic characterization of the first dicarbaporphyrin† Chemical Communications. 819-820. DOI: 10.1039/A809639B |
0.514 |
|
1999 |
Lash TD, Richter DT, Shiner CM. Conjugated Macrocycles Related to the Porphyrins. Part 16.1Synthesis of Hexa- and Heptaalkyl-Substituted Inverted or N-Confused Porphyrins by the “3 + 1” Methodology The Journal of Organic Chemistry. 64: 7973-7982. DOI: 10.1021/Jo991019R |
0.501 |
|
1999 |
Lash TD, Mani UN, Lyons EA, Thientanavanich P, Jones MA. Normal and Abnormal Heme Biosynthesis. 2.1Synthesis and Metabolism of Type-III Pentacarboxylic Porphyrinogens: Further Experimental Evidence for the Enzymic Clockwise Decarboxylation of Uroporphyrinogen-III The Journal of Organic Chemistry. 64: 478-487. DOI: 10.1021/Jo9814748 |
0.437 |
|
1999 |
Lash TD, Mani UN, Drinan MA, Zhen C, Hall T, Jones MA. Normal and Abnormal Heme Biosynthesis. 1. Synthesis and Metabolism of Di- and Monocarboxylic Porphyrinogens Related to Coproporphyrinogen-III and Harderoporphyrinogen: A Model for the Active Site of Coproporphyrinogen Oxidase The Journal of Organic Chemistry. 64: 464-477. DOI: 10.1021/Jo981473F |
0.362 |
|
1999 |
Rankin JG, Cantu R, Czernuszewicz RS, Lash TD. Fingerprinting petroporphyrin structures with vibrational spectroscopy. Part 5. Structural influences of the porphyrin 13-alkyl substituent on Resonance Raman scattering from nickel(II) cycloalkanoporphyrins Organic Geochemistry. 30: 201-228. DOI: 10.1016/S0146-6380(98)00215-0 |
0.38 |
|
1999 |
Richter DT, Lash TD. Oxidation with dilute aqueous ferric chloride solutions greatly improves yields in the ‘4+1’ synthesis of sapphyrins Tetrahedron Letters. 40: 6735-6738. DOI: 10.1016/S0040-4039(99)01352-0 |
0.375 |
|
1998 |
Hayes MJ, Spence JD, Lash TD. Facile oxidation of a carbaporphyrin at the internal carbon atom: synthesis of novel benzo[18]annulene ketals† Chemical Communications. 2409-2410. DOI: 10.1039/A806394J |
0.328 |
|
1998 |
Lash TD. The azuliporphyrin-carbaporphyrin connection† Chemical Communications. 1683-1684. DOI: 10.1039/A803575J |
0.315 |
|
1998 |
Lash TD, Chaney ST, Richter DT. Conjugated Macrocycles Related to the Porphyrins. 12.1Oxybenzi- and Oxypyriporphyrins: Aromaticity and Conjugation in Highly Modified Porphyrinoid Structures The Journal of Organic Chemistry. 63: 9076-9088. DOI: 10.1021/Jo981872A |
0.497 |
|
1998 |
Lash TD, Chandrasekar P, Osuma AT, Chaney ST, Spence JD. Porphyrins with Exocyclic Rings. 13.1Synthesis and Spectroscopic Characterization of Highly Modified Porphyrin Chromophores with Fused Acenaphthylene and Benzothiadiazole Rings The Journal of Organic Chemistry. 63: 8455-8469. DOI: 10.1021/Jo9815655 |
0.508 |
|
1998 |
Novak BH, Lash TD. Porphyrins with exocyclic rings. 11.1 Synthesis and characterization of phenanthroporphyrins, a new class of modified porphyrin chromophores Journal of Organic Chemistry. 63: 3998-4010. DOI: 10.1021/Jo980043M |
0.539 |
|
1998 |
Xu K, Rankin J, Lash TD. Infrared spectroscopy of geoporphyrins Vibrational Spectroscopy. 18: 175-186. DOI: 10.1016/S0924-2031(98)00064-2 |
0.358 |
|
1998 |
Xu K, Rankin J, Lash TD. Infrared spectroscopy of geoporphyrins Vibrational Spectroscopy. 18: 157-174. DOI: 10.1016/S0924-2031(98)00063-0 |
0.374 |
|
1998 |
Li W, Lash TD. Synthesis of deoxophylloerythroetioporphyrin (DPEP) and three ring homologs by an improved b-bilene methodology Tetrahedron Letters. 39: 8571-8574. DOI: 10.1016/S0040-4039(98)01960-1 |
0.373 |
|
1998 |
Bastian JA, Lash TD. Porphyrins with exocyclic rings. Part 12. Synthesis of meso,β-butano- and meso,β-pentanoporphyrins from cycloalka[b]pyrroles Tetrahedron. 54: 6299-6310. DOI: 10.1016/S0040-4020(98)00327-5 |
0.41 |
|
1998 |
Lash TD. Porphyrins with exocyclic rings. Part 10. Synthesis of meso,β-propanoporphyrins from 4,5,6,7-tetrahydro-1H-indoles Tetrahedron. 54: 359-374. DOI: 10.1016/S0040-4020(97)10288-5 |
0.502 |
|
1997 |
Lash TD, Wijesinghe C, Osuma AT, Patel JR. Synthesis of novel porphyrin chromophores from nitroarenes: Further applications of the Barton-Zard pyrrole condensation Tetrahedron Letters. 38: 2031-2034. DOI: 10.1016/S0040-4039(97)00287-6 |
0.475 |
|
1997 |
Chen S, Lash TD. Porphyrins with exocyclic rings. Part 8. Synthesis of nitrogen-15 and carbon-13 labeled 2,3:7,8:12,13:17,18-tetrabutanoporphyrin Journal of Heterocyclic Chemistry. 34: 273-278. DOI: 10.1002/Jhet.5570340141 |
0.357 |
|
1997 |
LASH TD. Porphyrins with Exocyclic Rings: Part 9 [1] Synthesis of Porphyrins by
the ‘3 + 1’ approach Journal of Porphyrins and Phthalocyanines. 1: 29-44. DOI: 10.1002/(Sici)1099-1409(199701)1:1<29::Aid-Jpp7>3.0.Co;2-S |
0.497 |
|
1996 |
Lash TD, Chandrasekar P. Synthesis of Tetraphenyltetraacenaphthoporphyrin: A New Highly Conjugated Porphyrin System with Remarkably Red-Shifted Electronic Absorption Spectra Journal of the American Chemical Society. 118: 8767-8768. DOI: 10.1021/Ja961227Q |
0.364 |
|
1996 |
Lash TD, Chaney ST. Conjugated macrocycles related to the porphyrins. Part 7.1 Tropiporphyrin: Tropylium versus porphyrinoid aromaticity Tetrahedron Letters. 37: 8825-8828. DOI: 10.1016/S0040-4039(96)02064-3 |
0.452 |
|
1996 |
Chandrasekar P, Lash TD. Versatile “3 + 1” syntheses of acenaphthoporphyrins, a new family of highly conjugated tetrapyrroles Tetrahedron Letters. 37: 4873-4876. DOI: 10.1016/0040-4039(96)00998-7 |
0.448 |
|
1996 |
Lash TD. Porphyrin Synthesis by the “3+1” Approach: New Applications for an Old Methodology Chemistry - a European Journal. 2: 1197-1200. DOI: 10.1002/Chem.19960021004 |
0.489 |
|
1996 |
Lash TD, Chaney ST. Oxypyriporphyrin, the First Fully Aromatic Porphyrinoid Macrocycle with a Pyridine Subunit Chemistry - a European Journal. 2: 944-948. DOI: 10.1002/Chem.19960020808 |
0.552 |
|
1995 |
Rankin JG, Czernuszewicz RS, Lash TD. Fingerprinting Petroporphyrin Structures with Vibrational Spectroscopy. 3. Resonance Raman Characterization of Regioisomers of Nickel(II) Tetrahydrobenzoporphyrin Inorganic Chemistry. 34: 3025-3037. DOI: 10.1021/Ic00115A033 |
0.335 |
|
1995 |
Rankin J, Czernuszewicz RS, Lash TD. Fingerprinting petroporphyrin structures with vibrational spectroscopy: II. Resonance Raman marker bands for the exocyclic rings of nickel tetrahydrobenzoporphyrins and nickel cycloalkanoporphyrins Organic Geochemistry. 23: 419-427. DOI: 10.1016/0146-6380(95)00016-8 |
0.376 |
|
1995 |
Lin V, Lash TD. Porphyrin synthesis by the “3 + 1” methodology: A superior approach for the preparation of porphyrins with fused 9,10-phenanthroline subunits Tetrahedron Letters. 36: 9441-9444. DOI: 10.1016/0040-4039(95)02100-0 |
0.451 |
|
1995 |
Lash TD, Novak BH. New highly conjugated porphyrin chromophores: Synthesis of mono- and diphenanthroporphyrins Tetrahedron Letters. 36: 4381-4384. DOI: 10.1016/0040-4039(95)00818-W |
0.428 |
|
1995 |
Lash TD, Denny CP. Porphyrins with exocyclic rings. Part 5. Synthesis of a naphtho[1,2-b]porphyrin. Tetrahedron. 51: 59-66. DOI: 10.1016/0040-4020(94)00963-U |
0.489 |
|
1995 |
Lash TD. Oxybenziporphyrin, a Fully Aromatic Semiquinone Porphyrin Analog with Pathways for 18π-Electron Delocalization Angewandte Chemie International Edition in English. 34: 2533-2535. DOI: 10.1002/Anie.199525331 |
0.308 |
|
1995 |
Lash TD. Oxybenziporphyrin, ein vollständig aromatisches Semichinon-Porphyrin-Analogon mit Delokalisierungsmöglichkeiten für 18 π-Elektronen Angewandte Chemie. 107: 2703-2705. DOI: 10.1002/Ange.19951072210 |
0.351 |
|
1994 |
Lash TD, Bellettini JR, Bastian JA, Couch KB. Synthesis of Pyrroles from Benzyl Isocyanoacetate Synthesis. 1994: 170-172. DOI: 10.1055/S-1994-25431 |
0.468 |
|
1994 |
Hu Z, Lash TD. Synthesis of a Porphyrin with Fused Five- and Seven-membered Exocyclic Rings from a Cross-conjugated Tetracyclic Dipyrrole Synlett. 1994: 909-910. DOI: 10.1055/S-1994-23044 |
0.412 |
|
1994 |
Lash TD, Nguyen TH, Hu Z. Reactivity of 1-Aza-1,4,5,6-tetrahydroazulenes and their Utility in the Preparation of Dipyrrolic Intermediates Needed for Petroporphyrin Synthesis Synlett. 1994: 905-908. DOI: 10.1055/S-1994-23043 |
0.433 |
|
1994 |
Lash TD, Drinan MA, Zhen C, Mani UN, Jones MA. Synthetic substrates for coproporophyrinogen oxidase: mesoporphyrinogen-VI revisited Bioorganic & Medicinal Chemistry Letters. 4: 1607-1612. DOI: 10.1016/S0960-894X(01)80575-8 |
0.393 |
|
1994 |
Lash TD, Novak BH, Lin Y. Synthesis of phenanthropyrroles and phenanthrolinopyrroles from isocyanoacetates: An extension of the barton-zard pyrrole condensation Tetrahedron Letters. 35: 2493-2494. DOI: 10.1016/S0040-4039(00)77152-8 |
0.445 |
|
1994 |
Lash TD, Roper TJ. Synthesis of dinaphthoporphyrins from dihydronaphtho[1,2-c]pyrroles Tetrahedron Letters. 35: 7715-7718. DOI: 10.1016/0040-4039(94)80100-2 |
0.456 |
|
1994 |
Drinan MA, Lash TD. Synthesis of benzyl and tert‐butyl 3‐(2‐methoxycarbonylethyl)‐4‐methylpyrrole‐2‐carboxylates from methyl 4‐oxobutanoate Journal of Heterocyclic Chemistry. 31: 255-257. DOI: 10.1002/Jhet.5570310144 |
0.373 |
|
1993 |
Lash TD, Quizon-Colquitt DM, Shiner CM, Nguyen TH, Hu Z. Recent advances in the synthesis of porphyrins with five-membered exocyclic rings Energy & Fuels. 7: 172-178. DOI: 10.1021/Ef00038A002 |
0.47 |
|
1993 |
Lash TD. Geochemical origins of sedimentary benzoporphyrins and tetrahydrobenzoporphyrins Energy & Fuels. 7: 166-171. DOI: 10.1021/Ef00038A001 |
0.325 |
|
1993 |
Lash TD, Catarello JJ. Porphyrins with exocyclic rings. Part 3. A reassessment on the utility of cyclopenta[b]pyrroles in the synthesis of porphyrin molecular fossils. Preparation of three type II porphyrins related to deoxophylloerythroetioporphyrin (DPEP). Tetrahedron. 49: 4159-4172. DOI: 10.1016/S0040-4020(01)85734-3 |
0.475 |
|
1993 |
Lash TD, Bellettini JR, Voiles SJ. One step synthesis of dihydropyrrolo[3,2‐e]indoles from 1,4‐cyclohexanedione Journal of Heterocyclic Chemistry. 30: 525-528. DOI: 10.1002/Jhet.5570300242 |
0.332 |
|
1993 |
Quizon-Colquitt DM, Lash TD. Porphyrins with exocyclic rings. Part 4. An improved one step synthesis of cyclopenta[b]pyrroles†‡ Journal of Heterocyclic Chemistry. 30: 477-482. DOI: 10.1002/Jhet.5570300233 |
0.455 |
|
1992 |
May DA, Lash TD. Porphyrins with exocyclic rings. 2. Synthesis of geochemically significant tetrahydrobenzoporphyrins from 4,5,6,7-tetrahydro-2H-isoindoles The Journal of Organic Chemistry. 57: 4820-4828. DOI: 10.1021/Jo00044A013 |
0.426 |
|
1992 |
Lash TD, Bladel KA, Shiner CM, Zajeski DL, Balasubramaniam RP. Porphyrins with exocyclic rings. 1. Chemistry of 4,5,6,7-tetrahydro-1H-indoles: synthesis of acetoxy derivatives, dihydroindoles, and novel porphyrins with four exocyclic rings Journal of Organic Chemistry. 57: 4809-4820. DOI: 10.1021/Jo00044A012 |
0.408 |
|
1992 |
Lash TD. Conjugated macrocycles related to the porphyrins. 4. Synthesis of a 23,24-dioxa-5-oxophlorin Journal of Organic Chemistry. 57: 4312-4315. DOI: 10.1021/Jo00041A051 |
0.401 |
|
1992 |
Armiger YLS, Lash TD. Conjugated macrocycles related to the porphyrins. Part 3 . Acid catalyzed condensations of thiophenecarboxaldehydes with a dipyrrylmethane Journal of Heterocyclic Chemistry. 29: 523-527. DOI: 10.1002/Jhet.5570290240 |
0.414 |
|
1991 |
Lash TD, Hoehner MC. An improved synthesis of pyrroles fromN-p-toluenesulfonylglycine esters and α,β-unsaturated aldehydes and ketones Journal of Heterocyclic Chemistry. 28: 1671-1676. DOI: 10.1002/Jhet.5570280705 |
0.344 |
|
1991 |
Lash TD, Armiger YLS. Conjugated macrocycles related to the porphyrins. Part2. Further synthetic and spectroscopic studies on difuryl analogs of the oxophlorins Journal of Heterocyclic Chemistry. 28: 965-970. DOI: 10.1002/Jhet.5570280421 |
0.445 |
|
1990 |
Lash TD, Balasubramaniam RP, Catarello JJ, Johnson MC, May DA, Bladel KA, Feeley JM, Hoehner MC, Marron TG. Influence of carbocyclic rings on porphyrin cyclizations: synthesis of geochemically significant cycloalkanoporphyrins Energy & Fuels. 4: 668-674. DOI: 10.1021/Ef00024A010 |
0.533 |
|
1989 |
Lash TD, Johnson MC. Total synthesis of the C31 and C32 15,17-butanoporphyrins from oil shales Tetrahedron Letters. 30: 5697-5698. DOI: 10.1016/S0040-4039(00)76173-9 |
0.417 |
|
1989 |
Lash TD. Synthesis of the porphyrins from petroleum Organic Geochemistry. 14: 213-225. DOI: 10.1016/0146-6380(89)90076-4 |
0.487 |
|
1988 |
Lash TD. On the modifying influence of six-membered carbocyclic rings in porphyrin cyclizations: Synthesis of meso, β-propanoporphyrins Tetrahedron Letters. 29: 6877-6880. DOI: 10.1016/S0040-4039(00)88464-6 |
0.421 |
|
1987 |
Lash TD, Bladel KA, Johnson MC. Synthesis of porphyrins with four exocyclic rings from 4,5,6,7-tetrahydroindoles Tetrahedron Letters. 28: 1135-1138. DOI: 10.1016/S0040-4039(00)95308-5 |
0.39 |
|
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