A novel thermolytic distillation process was developed to depolymerize polyhydroxybutyrate (PHB) for the selective production of crotonic acid. The conditions adopted (170°C, 150 mbar) were applied to pure PHB and...
The site-selective dearomatization of naphthols is realized in a straightforward manner through a gold(I)-catalyzed [3,3]-sigmatropic rearrangement/allene functionalization cascade sequence. The method employs readily available naphthylpropargyl ethers as starting materials. A range of densely functionalized dihydrofurylnaphthalen-2(1H)-ones are obtained in high yields (up to 98 %) and extremely mild reaction conditions (reagent grade solvent, air, 10 minute reaction time). A complete theoretical elucidation of the reaction machinery is also proposed, providing a rationale for important issues such as regio- and chemoselectivity.
Two novel protocols
for the chemical valorization of polyhydroxybutyrate
(PHB) were developed, aiming at the production of two bio-based molecules:
methyl 3-hydroxybutyrate (MHB) and methyl 3-methoxybutyrate (MMB).
Optimized reaction conditions were applied to pure PHB and PHB inclusions
inside bacterial cells as starting materials. MHB was synthesized
through a single-step catalytic methanolysis, while MMB was synthesized
through a three-step process: thermolytic distillation to give crotonic
acid (CA), esterification to give methyl crotonate (MC), and oxa-Michael
addition of MeOH. The obtained MHB and MMB were tested as solvents
for the recovery of PHB itself both from freeze-dried single strain
cultures (SSC) and mixed microbial cultures (MMC) with low to medium
contents of PHB (22–57 wt %). High PHB recovery was achieved:
up to 96 ± 1% through MHB and up to 98 ± 1% through MMB.
Extraction from MMC slurry (with a PHB content of 39% on dry weight)
was also performed, recovering 77 ± 2% using MHB and 92 ±
2% using MMB. High purities and excellent molecular weights and polydispersity
indexes of extracted PHB were obtained with both MHB and MMB. Solubility
in water, octanol/water partition coefficients (log K
ow), and aerobic ready biodegradability of both solvents
were also evaluated.
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