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Vibrational Circular Dichroism Detects Symmetry Breaking due to Conformational Mobility in C 2 -Symmetry Chiral Molecules and Provides Further Insight into Inter-Chromophoric Interactions.
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- Symmetry (20738994), 2020, v. 12, n. 11, p. 1752, doi. 10.3390/sym12111752
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- Article
N<sub>21</sub>,N<sub>22</sub>-carbonyl-bridged biliverdin. red-blue color change effected by conformation.
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- Journal of Heterocyclic Chemistry, 2005, v. 42, n. 1, p. 161, doi. 10.1002/jhet.5570420126
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- Article
Strongly fluorescent dipyrrinones-substituent effects.
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- Journal of Heterocyclic Chemistry, 2004, v. 41, n. 6, p. 1033, doi. 10.1002/jhet.5570410631
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Syntheses and properties of benzodipyrrinones.
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- Journal of Heterocyclic Chemistry, 2003, v. 40, n. 1, p. 181, doi. 10.1002/jhet.5570400127
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On the aggregation of bilirubins using vapor pressure osmometry.
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- Journal of Heterocyclic Chemistry, 2000, v. 37, n. 4, p. 863, doi. 10.1002/jhet.5570370431
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Synthesis and conformational analysis of a chiral fluorinated bilirubin analog lacking carboxyl groups.
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- Journal of Heterocyclic Chemistry, 1999, v. 36, n. 4, p. 969, doi. 10.1002/jhet.5570360424
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Intensely fluorescent dipyrrinones.
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- Journal of Physical Organic Chemistry, 2004, v. 17, n. 8, p. 675, doi. 10.1002/poc.755
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Carboxylic acid ionization constants by <sup>19</sup>F NMR spectroscopy.
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- Journal of Physical Organic Chemistry, 1999, v. 12, n. 10, p. 751, doi. 10.1002/(SICI)1099-1395(199910)12:10<751::AID-POC190>3.0.CO;2-P
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Cover Image, Volume 30, Issue 1.
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- Chirality, 2018, v. 30, n. 1, p. i, doi. 10.1002/chir.22802
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On the aggregation of bilirubinoids in solution as evidenced by VCD and ECD spectroscopy and DFT calculations.
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- Chirality, 2018, v. 30, n. 1, p. 19, doi. 10.1002/chir.22776
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Insights into the Structures of Bilirubin and Biliverdin from Vibrational and Electronic Circular Dichroism: History and Perspectives.
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- Molecules, 2023, v. 28, n. 6, p. 2564, doi. 10.3390/molecules28062564
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Exciton chirality in trans-1,2-diamidocyclohexanes: Fluorescent chromophores.
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- Chirality, 2005, v. 17, n. 6, p. 316, doi. 10.1002/chir.20170
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Chirality inversion in the bilirubin molecular exciton.
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- Chirality, 2001, v. 13, n. 5, p. 251, doi. 10.1002/chir.1027
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Relative steric size of SCH<sub>3</sub>, OCH<sub>3</sub>, and CH<sub>3</sub> groups from circular dichroism measurements.
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- Chirality, 2000, v. 12, n. 4, p. 204, doi. 10.1002/(SICI)1520-636X(2000)12:4<204::AID-CHIR7>3.0.CO;2-C
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- Article
Exciton chirality of bilirubin homologs.
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- Chirality, 1997, v. 9, n. 5/6, p. 604, doi. 10.1002/(SICI)1520-636X(1997)9:5/6<604::AID-CHIR31>3.0.CO;2-Q
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- Article