Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Orlando D. C. C. de Azevedo"'
Autor:
Christopher Pullen, Paul I. P. Elliott, Christopher D. Gabbutt, B. Mark Heron, Orlando D. C. C. de Azevedo, Kyle Jack Lord
Publikováno v:
The Journal of Organic Chemistry. 85:10772-10796
Multitarget synthetic strategies to access novel photochromic 3H-naphtho[2,1-b]pyrans decorated with pyridyl units are described. The new pyridyl-substituted 3H-naphtho[2,1-b]pyrans display good photochromic properties with reversible generation of p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3acde27c91ade9736c9ac1766c59371c
https://doi.org/10.1021/acs.joc.0c01296
https://doi.org/10.1021/acs.joc.0c01296
Autor:
Orlando D. C. C. de Azevedo, Thomas Driscoll, Kieran Chauhan, Stuart Aiken, B. Mark Heron, Paul I. P. Elliott, Christopher D. Gabbutt
Publikováno v:
The Journal of Organic Chemistry. 85:952-966
A study of the ring-contraction of a model 3H-naphtho[2,1-b]pyran is described to elucidate and optimize the ring-contraction of naphthopyrans. Two efficient base-mediated protocols to access multi...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e678b04a6ca4a1baf07cb20899d01a8
https://doi.org/10.1021/acs.joc.9b02901
https://doi.org/10.1021/acs.joc.9b02901
Autor:
Mike W. J. Urquhart, Abby J. Mills, B. Mark Heron, Stuart Aiken, Ross J.L. Edgar, Lewis Cowen, Orlando D. C. C. de Azevedo, Craig R. Rice, Kelechi Anozie, Philippa A. Lawrence, Christopher D. Gabbutt, Dimitrios Zonidis
Publikováno v:
Organic & Biomolecular Chemistry. 17:9585-9604
Diversely substituted 1,2-oxathiine 2,2-dioxides, including 3,5,6-triaryl-, 3,6-diaryl-, 3,5-diaryl-, 5,6-diaryl- and selected fused heterocyclic analogues, have been efficiently obtained by the application of a mild Cope elimination of a 4-amino moi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2c27639f0b9031c0ab9898cc1bf566e
https://doi.org/10.1039/c9ob01657k
https://doi.org/10.1039/c9ob01657k
Autor:
Craig R. Rice, Orlando D. C. C. de Azevedo, Denis Jacquemin, Christopher D. Gabbutt, Paul A. Scattergood, Mark Heron, Paul I. P. Elliott
Publikováno v:
Dalton Transactions
Dalton Transactions, Royal Society of Chemistry, 2021, 50 (3), pp.830-834. ⟨10.1039/d0dt04220j⟩
Dalton Transactions, Royal Society of Chemistry, 2021, 50 (3), pp.830-834. ⟨10.1039/d0dt04220j⟩
International audience; Re(i) complexes bearing thermally reversible photochromic naphthopyran axial ligands undergo highly efficient, reversible phosphorescence quenching actuated by either visible or UV irradiation. The photoinduced quenching of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54a13b2b462c8b808cbdcf1f09a49cbe
https://pubmed.ncbi.nlm.nih.gov/33427837
https://pubmed.ncbi.nlm.nih.gov/33427837
Publikováno v:
Synlett. 26:1379-1384
A novel route for the synthesis of new (E)-8-styrylflavones is reported. This methodology involves the regio- and stereoselective Heck cross-coupling reaction of 8-iodoflavones and styrene derivatives. The Heck precursors, 8-iodoflavones, were obtain
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::57615f54760b9602f59042bd245ac07b
https://doi.org/10.1055/s-0034-1380208
https://doi.org/10.1055/s-0034-1380208