Tetrahedron, volume 54, issue 22, pages 6147-6158

Reactions of chloromethyl aryl sulfones carbanions with anthraquinone derivatives

Mieczysz Shtslslaw Ma̧kosza 1
, 
Shamil Nizamov 1
, 
Zofia Urbańczyk-Lipkowska 1
1
 
Institute of Organic Chemistry Polish Academy of Sciences, Kasprzaka 44/52, 01-224 Warsaw (Poland). | 
Publication type: Journal Article
Publication date: 1998-05-01
Journal: Tetrahedron
scimago Q3
wos Q2
SJR: 0.406
CiteScore: 3.9
Impact factor: 2.1
ISSN: 00404020, 14645416
Organic Chemistry
Drug Discovery
Biochemistry
Abstract
Carbanions of chloromethyl phenyl sulfone and chloromethyl p -tolyl sulfone react with anthraquinone containing electrondonating substituents in two major ways: vicarious nucleophilic substitution (VNS) of hydrogen and addition to the carbonyl group. The reaction course depends on electrondonating effects of these substituents-strong electron donors promote the VNS reaction. Graphic
Found 0
By date By citations
Found 0
By date By citations

Top-30

Journals

1
Tetrahedron
Tetrahedron, 1, 33.33%
ChemInform
ChemInform, 1, 33.33%
1

Publishers

1
Elsevier
Elsevier, 1, 33.33%
Wiley
Wiley, 1, 33.33%
1
  • We do not take into account publications without a DOI.
  • Statistics recalculated only for publications connected to researchers, organizations and labs registered on the platform.
  • Statistics recalculated weekly.

Are you a researcher?

Create a profile to get free access to personal recommendations for colleagues and new articles.
Metrics
Share
Cite this
GOST | RIS | BibTex | MLA
Found error?