TY - JOUR
T1 - Exploiting Chitin as a Source of Biologically Fixed Nitrogen
T2 - Formation and Full Characterization of Small-Molecule Hetero- and Carbocyclic Pyrolysis Products
AU - Nikahd, Maryam
AU - Mikusek, Jiri
AU - Yu, Li Juan
AU - Coote, Michelle L.
AU - Banwell, Martin G.
AU - Ma, Chenxi
AU - Gardiner, Michael G.
PY - 2020/4/3
Y1 - 2020/4/3
N2 - Pyrolysis of variously pretreated or untreated samples of chitin (1) and certain congeners at 150-350 °C afforded a range of platform molecules, as exemplified by compounds 4, 5, 6, 8, 12 and 13. All of these products have been fully characterized, including by single-crystal X-ray analysis. Pathways for the formation of them are proposed and theoretical studies of certain aspects of these described.
AB - Pyrolysis of variously pretreated or untreated samples of chitin (1) and certain congeners at 150-350 °C afforded a range of platform molecules, as exemplified by compounds 4, 5, 6, 8, 12 and 13. All of these products have been fully characterized, including by single-crystal X-ray analysis. Pathways for the formation of them are proposed and theoretical studies of certain aspects of these described.
KW - Chitin
KW - Nitrogen
KW - mall-Molecule Hetero
KW - Carbocyclic Pyrolysis
UR - http://www.scopus.com/inward/record.url?scp=85084207631&partnerID=8YFLogxK
UR - http://purl.org/au-research/grants/ARC/FL170100041
UR - http://purl.org/au-research/grants/ARC/CE140100012
U2 - 10.1021/acs.joc.9b03438
DO - 10.1021/acs.joc.9b03438
M3 - Article
C2 - 32019306
AN - SCOPUS:85084207631
SN - 0022-3263
VL - 85
SP - 4583
EP - 4593
JO - Journal of Organic Chemistry
JF - Journal of Organic Chemistry
IS - 7
ER -