A Novel Aromatic Iodination Method Using F2

Shlomo Rozen; Dov Zamir

doi:10.1021/jo00298a032

A Novel Aromatic Iodination Method Using F₂

Shlomo Rozen, Dov Zamir

School of Chemistry

Research output: Contribution to journal › Article › peer-review

Abstract

A new method for direct aromatic iodination with IF, made in situ from the corresponding elements, is described. Depending on the reaction time and temperature, mono- or polyiodination can be achieved. Even deactivated aromatic rings can be directly iodinated without the presence of any Friedel—Crafts catalyst. Sensitive groups such as aromatic aldehydes are not affected by the reagent.

Original language	English
Pages (from-to)	3552-3555
Number of pages	4
Journal	Journal of Organic Chemistry
Volume	55
Issue number	11
DOIs	https://doi.org/10.1021/jo00298a032
State	Published - 1990

Access to Document

10.1021/jo00298a032

Cite this

@article{d7b023c6edf24936837d80ac9930490b,

title = "A Novel Aromatic Iodination Method Using F2",

abstract = "A new method for direct aromatic iodination with IF, made in situ from the corresponding elements, is described. Depending on the reaction time and temperature, mono- or polyiodination can be achieved. Even deactivated aromatic rings can be directly iodinated without the presence of any Friedel—Crafts catalyst. Sensitive groups such as aromatic aldehydes are not affected by the reagent.",

author = "Shlomo Rozen and Dov Zamir",

year = "1990",

doi = "10.1021/jo00298a032",

language = "אנגלית",

volume = "55",

pages = "3552--3555",

journal = "Journal of Organic Chemistry",

issn = "0022-3263",

publisher = "American Chemical Society",

number = "11",

}

TY - JOUR

T1 - A Novel Aromatic Iodination Method Using F2

AU - Rozen, Shlomo

AU - Zamir, Dov

PY - 1990

Y1 - 1990

N2 - A new method for direct aromatic iodination with IF, made in situ from the corresponding elements, is described. Depending on the reaction time and temperature, mono- or polyiodination can be achieved. Even deactivated aromatic rings can be directly iodinated without the presence of any Friedel—Crafts catalyst. Sensitive groups such as aromatic aldehydes are not affected by the reagent.

AB - A new method for direct aromatic iodination with IF, made in situ from the corresponding elements, is described. Depending on the reaction time and temperature, mono- or polyiodination can be achieved. Even deactivated aromatic rings can be directly iodinated without the presence of any Friedel—Crafts catalyst. Sensitive groups such as aromatic aldehydes are not affected by the reagent.

UR - http://www.scopus.com/inward/record.url?scp=2942725815&partnerID=8YFLogxK

U2 - 10.1021/jo00298a032

DO - 10.1021/jo00298a032

M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???

AN - SCOPUS:2942725815

VL - 55

SP - 3552

EP - 3555

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

SN - 0022-3263

IS - 11

ER -

A Novel Aromatic Iodination Method Using F₂

Abstract

Access to Document

Other files and links

Fingerprint

Cite this