Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Peter P, Molesworth"'
Autor:
Astrid Hyldbakk, Yrr Mørch, Sofie Snipstad, Andreas K.O. Åslund, Geir Klinkenberg, Vu To Nakstad, Ane-Marit Wågbø, Ruth Schmid, Peter P. Molesworth
Publikováno v:
International Journal of Pharmaceutics: X, Vol 4, Iss , Pp 100124- (2022)
Poly (alkyl cyanoacrylate) (PACA) polymeric nanoparticles (NPs) are promising drug carriers in drug delivery. However, the selection of commercially available alkyl cyanoacrylate (ACA) monomers is limited, because most monomers were designed for use
Externí odkaz:
https://doaj.org/article/25e19769b35c47c6b4460205bdec8409
Autor:
Wilhelm Robert Glomm, Peter Patrick Molesworth, Eugenia Mariana Sandru, Le Thuy Truong, Anders Brunsvik, Heidi Johnsen
Publikováno v:
Applied Sciences, Vol 11, Iss 9, p 3956 (2021)
Most liquid food flavours such as essential oils are volatile and prone to degradation in the presence of oxygen, light, moisture and high temperatures. Microencapsulation of volatile ingredients prior to use in food or beverages is a commonly used p
Externí odkaz:
https://doaj.org/article/16eed10ecaf543019a87a2f39f9e3b3e
Autor:
Astrid, Hyldbakk, Yrr, Mørch, Sofie, Snipstad, Andreas K O, Åslund, Geir, Klinkenberg, Vu To, Nakstad, Ane-Marit, Wågbø, Ruth, Schmid, Peter P, Molesworth
Publikováno v:
International Journal of Pharmaceutics: X
Poly (alkyl cyanoacrylate) (PACA) polymeric nanoparticles (NPs) are promising drug carriers in drug delivery. However, the selection of commercially available alkyl cyanoacrylate (ACA) monomers is limited, because most monomers were designed for use
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24a6e2892d37ee70389e9b01684e0566
https://hdl.handle.net/11250/3065045
https://hdl.handle.net/11250/3065045
Autor:
Peter P. Molesworth
Publikováno v:
Comprehensive Heterocyclic Chemistry IV ISBN: 9780128186565
Comprehensive Heterocyclic Chemistry IV
Comprehensive Heterocyclic Chemistry IV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f5c3b5e7e85762345803c8ce61cbe49f
https://doi.org/10.1016/b978-0-12-818655-8.00116-5
https://doi.org/10.1016/b978-0-12-818655-8.00116-5
Publikováno v:
Tetrahedron. 72:2084-2093
The formation of the macrocyclic core of crassin acetate from an acyclic precursor could be effected by ring-closing alkyne metathesis reactions while ring-closing olefin metathesis reactions failed. Installment of necessary stereochemistry was achie
Autor:
Jason A. Smith, Peter P. Molesworth, Sandra E. Davidson, Nathan D. Tivendale, James B. Reid, John Ross, Noel W. Davies, Edwin K. Lowe
Publikováno v:
Plant Physiology. 154:1957-1965
The tryptamine pathway is one of five proposed pathways for the biosynthesis of indole-3-acetic acid (IAA), the primary auxin in plants. The enzymes AtYUC1 (Arabidopsis thaliana), FZY (Solanum lycopersicum), and ZmYUC (Zea mays) are reported to catal
Publikováno v:
Rapid Communications in Mass Spectrometry. 24:1105-1110
It has been demonstrated that substituted indoles fully labelled with deuterium on the aromatic ring can undergo substantial exchange back to partial and even fully protonated forms during atmospheric pressure chemical ionisation (APCI) liquid chroma
Autor:
Peter P. Molesworth, Paul W. Walker, Jason A. Smith, Geoff R. Allen, Fredrik Andersson, Anna Nilsson, Erik Hedenström, Noel W. Davies
Publikováno v:
Journal of Chemical Ecology. 35:1411-1422
The sex pheromone of Mnesampela privata, an endemic pest of Eucalyptus plantations in Australia, was previously identified as a single bioactive compound, (3Z,6Z,9Z)-3,6,9-nonadecatriene (C19 triene). Initial field testing of lures containing 1 mg, 5
Autor:
Nathan D. Tivendale, Peter P. Molesworth, Noel W. Davies, John Ross, Jason A. Smith, Laura J. Quittenden
Publikováno v:
Plant Physiology. 151:1130-1138
One pathway leading to the bioactive auxin, indole-3-acetic acid (IAA), is known as the tryptamine pathway, which is suggested to proceed in the sequence: tryptophan (Trp), tryptamine, N-hydroxytryptamine, indole-3-acetaldoxime, indole-3-acetaldehyde
Publikováno v:
Tetrahedron. 61:8226-8230
The nucleophilicity of pyrrole has been exploited to rapidly assemble the bicyclic skeleton of the indolizidine alkaloids. The key sequence is the annulation of a second ring onto pyrrole from a γ-lactone and has been exploited in the synthesis of t