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Importance of C4a- and N5-covalent adducts in the flavin oxidation of carbanions.
Biochemistry. 1978 Oct 31;17(22):4784-93. doi: 10.1021/bi00615a028.

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2
Characterization and postulated structure of the primary emitter in the bacterial luciferase reaction.
Proc Natl Acad Sci U S A. 1984 May;81(10):2990-4. doi: 10.1073/pnas.81.10.2990.

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1
Spectral properties of an oxygenated luciferase-flavin intermediate isolated by low-temperature chromatography.
Proc Natl Acad Sci U S A. 1973 Dec;70(12 Pt 1-2):3468-72. doi: 10.1073/pnas.70.12.3468.
2
Decyl nitrite: an aldehyde analog in the bacterial bioluminescence reaction.
Biochem Biophys Res Commun. 1974 Feb 27;56(4):865-8. doi: 10.1016/s0006-291x(74)80268-8.
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A postulated mechanism for the bioluminescent oxidation of reduced flavin mononucleotide.
Biochem Biophys Res Commun. 1972 Apr 28;47(2):348-53. doi: 10.1016/0006-291x(72)90719-x.
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Radical mechanisms for 1,5-dihydro-5-methylflavine reduction of carbonyl compounds.
J Am Chem Soc. 1975 Sep 3;97(18):5263-71. doi: 10.1021/ja00851a041.
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The chemistry of an N5-methyl-1,5-dihydroflavin and its aminium cation radical.
J Am Chem Soc. 1976 Jun 23;98(13):3955-64. doi: 10.1021/ja00429a035.

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