Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Christopher, Wicks"'
Publikováno v:
IUCrData, Vol 5, Iss 3, p x200288 (2020)
In the title compound, C14H14O, the seven-membered ring is in a pseudo-chair conformation. In the crystal, molecules are linked by weak C—H...O hydrogen bonds forming layers parallel to (010). In addition, there are weak π–π stacking interactio
Externí odkaz:
https://doaj.org/article/905ae8a483e640289c20fee0731cb472
Autor:
Jeffrey Davidson, Charles Gauthier-Signore, Kevin P. Bishop, Christopher Wicks, Mario A. Monteiro, Pierre-Nicholas Roy, France-Isabelle Auzanneau
Publikováno v:
Organic & Biomolecular Chemistry. 20:2964-2980
CH3-6 of l-Rha and H-2 of d-Man give ROE correlation in the α-d-Manp-(1 → 4)-l-Rhap motif. C-2 in d-Man is shifted upfield in the 13C NMR spectrum of the β-d-Rhap-(1 → 3)-d-Manp motif.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c45ceb12af4acb301fc33fad3a69b26c
https://doi.org/10.1039/d2ob00131d
https://doi.org/10.1039/d2ob00131d
Autor:
Jeffrey, Davidson, Charles, Gauthier-Signore, Kevin P, Bishop, Christopher, Wicks, Mario A, Monteiro, Pierre-Nicholas, Roy, France-Isabelle, Auzanneau
Publikováno v:
Organicbiomolecular chemistry. 20(14)
Many children suffering from autism spectrum disorder (ASD) experience gastrointestinal (GI) conditions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b12c93325db86b4f1585e94532658ea8
https://pubmed.ncbi.nlm.nih.gov/35333269
https://pubmed.ncbi.nlm.nih.gov/35333269
Publikováno v:
The Alkaloids. Chemistry and biology. 86
This chapter provides a short overview of the history of morphine since it's isolation by Sertürner in 1805. The biosynthesis of the title alkaloid as well as all total and formal syntheses of morphine and codeine published after 1996 are discussed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3dab764a46fcbf4f9e87e3e3b0e514eb
https://pubmed.ncbi.nlm.nih.gov/34565506
https://pubmed.ncbi.nlm.nih.gov/34565506
Publikováno v:
The Alkaloids: Chemistry and Biology ISBN: 9780128246184
This chapter provides a short overview of the history of morphine since it's isolation by Serturner in 1805. The biosynthesis of the title alkaloid as well as all total and formal syntheses of morphine and codeine published after 1996 are discussed i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b15d9c938626cd5e10fefec12d9597b
https://doi.org/10.1016/bs.alkal.2021.04.001
https://doi.org/10.1016/bs.alkal.2021.04.001
Publikováno v:
IUCrData, Vol 5, Iss 3, p x200288 (2020)
In the title compound, C14H14O, the seven-membered ring is in a pseudo-chair conformation. In the crystal, molecules are linked by weak C—H...O hydrogen bonds forming layers parallel to (010). In addition, there are weak π–π stacking interactio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc5a769c3b6b9c47e143282788b7107d
http://scripts.iucr.org/cgi-bin/paper?S2414314620002886
http://scripts.iucr.org/cgi-bin/paper?S2414314620002886
Publikováno v:
IUCrData. 5(Pt 3)
In the title compound, C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::879b65221dab46b3f40b5e676e2dc259
https://pubmed.ncbi.nlm.nih.gov/36339480
https://pubmed.ncbi.nlm.nih.gov/36339480
Publikováno v:
Tetrahedron Letters. 60:151228
An investigation of intramolecular ring-opening reactions of various cyclopropanated oxabenzonorbornadienes (CPOBDs) with alcohol nucleophiles is reported, which forms two regioisomeric products in good yields. The effect of various tether lengths wa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2b6e810e79292e971150880c37350388
https://doi.org/10.1016/j.tetlet.2019.151228
https://doi.org/10.1016/j.tetlet.2019.151228
Publikováno v:
Tetrahedron Letters. 60:150990
The iridium-catalyzed ring-opening reaction of unsymmetrical oxabenzonorbornadienes (OBD) with water and alcohol nucleophiles is reported, with the effects of various C1-substituents explored. Electron-donating alkyl groups lead entirely to the subst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::525819982efef35229f5e9f9667e7a06
https://doi.org/10.1016/j.tetlet.2019.150990
https://doi.org/10.1016/j.tetlet.2019.150990
Autor:
and Timothy C. Walsgrove, Clive J. Moores, Richard Neville Saunders, Jerome F. Hayes, Richard J. Atkins, Lynne P. Crawford, Michael Anthony Harris, Christopher Wicks, Gary F. Breen, Trevor J. Grinter, Andrew C. Share
Publikováno v:
Organic Process Research & Development. 1:185-197
The 3,4,8-trisubstituted quinoline derivatives 2-butyryl-8-methoxy-4-[(2-methylphenyl)amino]quinoline and 3-butyryl-8-(2-hydroxyethoxy)-4-[(2-methylphenyl)amino]quinoline were prepared using five novel synthetic strategies, each involving a different
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::71bb87bb1625590969f1c2a8b0464cfc
https://doi.org/10.1021/op9700035
https://doi.org/10.1021/op9700035