Please use this identifier to cite or link to this item: http://hdl.handle.net/11189/6442
DC FieldValueLanguage
dc.contributor.authorGreen, Ivan Ren_US
dc.contributor.authorHugo, Victor Ien_US
dc.contributor.authorMei, Mawonga Nen_US
dc.date.accessioned2018-07-11T09:38:13Z-
dc.date.available2018-07-11T09:38:13Z-
dc.date.issued2006-
dc.identifier.citationGreen, I.R., Hugo, V.I. and Mei, M.N.2006. Bromination Products of 2‐Substituted 5, 7‐Dimethoxy‐4‐Naphthols. Synthetic communications, 36(3): 331-346en_US
dc.identifier.issn0039-7911-
dc.identifier.urihttp://hdl.handle.net/11189/6442-
dc.description.abstractBromination in acetic acid is favored at C‐8 in 5,7‐dimethoxy‐4‐naphthol when the C‐2 substituent is methyl carboxylate, whereas C‐1 is favored when the C‐2 substituent is either acetoxymethylene or methyl.en_US
dc.language.isoenen_US
dc.publisherTaylor & Francisen_US
dc.relation.ispartofSynthetic Communicationsen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/za/-
dc.subject2‐Acetoxymethyl‐5,7‐dimethoxy‐4‐naphtholen_US
dc.subjectBrominationsen_US
dc.subject5,7‐dimethoxy‐2‐methyl‐4‐naptholen_US
dc.subjectMethyl 5,7‐dimethoxy‐4‐hydroxy‐2‐naphthoateen_US
dc.titleBromination products of 2-subsituted 5,7-dimethoxy-4-naphthols.en_US
dc.type.patentArticleen_US
dc.identifier.doihttps://doi.org/10.1080/00397910500377370-
Appears in Collections:Appsc - Journal Articles (DHET subsidised)
Files in This Item:
File Description SizeFormat 
Bromination products.pdf184.46 kBAdobe PDFView/Open
Show simple item record

Page view(s)

73
Last Week
0
Last month
1
checked on Aug 12, 2026

Download(s)

18
checked on Aug 12, 2026

Google ScholarTM

Check

Altmetric


This item is licensed under a Creative Commons License Creative Commons