flavin-adenine-dinucleotide and spiropentaneacetic-acid

Both diastereomeric 4-butylspiropentylcarbinyl bromides (14a and 14b) were synthesized in seven steps starting from 1-heptyne, and the stereochemical assignments based upon NOE experiments were confirmed by converting their immediate alcohol precursors (13a and 13b) to 1,4-dibutylspiropentanes (17a and 17b) with C(1) and C(2) symmetry. Each bromide was used to generate its corresponding spiropentylcarbinyl radical (18a and 18b) via its AIBN-initiated tri-n-butyltin hydride reduction. The radical-trapped products are identified, the preferred ring scission mode is identified (C1[bond] C2 bond cleavage), and the estimated rates for the ring opening of 4-butylspiropentylcarbinyl radical (18, k(25) degrees C > or = approximately 5 x 10(9) s(-1)) and 2-butyl-1-vinylcyclopropylcarbinyl radical (33, k(25) degrees C approximately 5 x 10(8) s(-1)) are reported. High-level ab initio calculations addressing the ring-opening isomerizations of cyclopropylcarbinyl and spiropentylcarbinyl radicals also are presented. These results in conjunction with a previous study enable us to propose two structures for the enzyme-catalyzed FAD adducts resulting from spiropentylacetic acid-CoA, a synthetic byproduct of fatty acid metabolism.

Topics: Coenzyme A; Flavin-Adenine Dinucleotide; Free Radicals; Models, Chemical; Molecular Mimicry; Nucleic Acid Conformation; Spiro Compounds