Mark A Honey - Publications
Affiliations: | Faculty of Engineering and Science | University of Greenwich |
Area:
Organic chemistry, medicinal chemistryWebsite:
https://honeyresearchgroup.comYear | Citation | Score | |||
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2018 | Henderson SH, West RA, Ward SE, Honey MA. Metal-free selective mono-halodecarboxylation of heteroarenes under mild conditions. Royal Society Open Science. 5: 180333. PMID 30110478 DOI: 10.1098/Rsos.180333 | 0.355 | |||
2016 | Mallinger A, Schiemann K, Rink C, Sejberg J, Honey MA, Czodrowski P, Stubbs M, Poeschke O, Busch M, Schneider R, Schwarz D, Musil D, Burke R, Urbahns K, Workman P, et al. 2,8-Disubstituted-1,6-Naphthyridines and 4,6-Disubstituted-Isoquinolines with Potent, Selective Affinity for CDK8/19. Acs Medicinal Chemistry Letters. 7: 573-8. PMID 27326329 DOI: 10.1021/Acsmedchemlett.6B00022 | 0.413 | |||
2014 | Honey MA, Yamashita Y, Kobayashi S. A cooperative water effect in proazaphosphatrane-catalysed heterocycle synthesis. Chemical Communications (Cambridge, England). 50: 3288-91. PMID 24525763 DOI: 10.1039/C3Cc49808E | 0.393 | |||
2014 | Honey MA, Moody CJ. Synthesis of indoxylic acid esters by rhodium-catalyzed carbene n-h insertion and thermal cyclization Australian Journal of Chemistry. 67: 1211-1216. DOI: 10.1071/Ch14116 | 0.473 | |||
2012 | Honey MA, Pasceri R, Lewis W, Moody CJ. Diverse trifluoromethyl heterocycles from a single precursor. The Journal of Organic Chemistry. 77: 1396-405. PMID 22264218 DOI: 10.1021/Jo202201W | 0.475 | |||
2009 | Honey MA, Blake AJ, Campbell IB, Judkins BD, Moody CJ. One-pot synthesis of N-methylindoles from N-methylanilines and of benzofurans from phenols using transition-metal carbene X-H insertion reactions Tetrahedron. 65: 8995-9001. DOI: 10.1016/J.Tet.2009.07.077 | 0.463 | |||
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