Are bis(pyridine)iodine(i) complexes applicable for asymmetric halogenation?-Reference-Cited by-同舟云学术

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Are bis(pyridine)iodine(i) complexes applicable for asymmetric halogenation?

Published:2021 Issue:38 Volume:19 Page:8307-8323
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

von der Heiden Daniel¹^ORCID,Németh Flóra Boróka²,Andreasson Måns³^ORCID,Sethio Daniel¹^ORCID,Pápai Imre²⁴^ORCID,Erdelyi Mate¹^ORCID

Affiliation:

1. Department of Chemistry – BMC, Uppsala University, SE-751 23 Uppsala, Sweden

2. Institute of Organic Chemistry, Research Centre for Natural Sciences, H-1117 Budapest, Hungary

3. Department of Chemistry and Molecular Biology, University of Gothenburg, SE-412 96 Gothenburg, Sweden

4. Department of Chemistry, University J. Selyeho, 94505 Komárno, Slovakia

Abstract

The enantioselectivity of the iodine(i) transfer process from chiral bis(pyridine)iodine(i) complexes to alkenes is explored.

Funder

European Regional Development Fund

FP7 Ideas: European Research Council

Vetenskapsrådet

VINNOVA

Svenska Forskningsrådet Formas

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/OB/D1OB01532J

Reference84 articles.

1. The Halogenation of Ethylenes

2. The Mechanism of Addition Reactions. A Kinetic Study of the Addition of Methyl Hypobromite to Stilbene

3. C. K.Ingold , Structure and Mechanism in Organic Chemistry , Cornell University Press , Ithaca , 1953

4. Stable carbonium ions. XXXIII. Primary alkoxycarbonium ions

5. stable carbonium ions. lvii catalysts with olefins.ang. .ang.

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