Novel Oxidative α-Tosyloxylation of Alcohols with Iodosylbenzene and p-Toluenesulfonic Acid and Its Synthetic Use for Direct Preparation of Heteroaromatics-Reference-Cited by-同舟云学术

Novel Oxidative α-Tosyloxylation of Alcohols with Iodosylbenzene and p-Toluenesulfonic Acid and Its Synthetic Use for Direct Preparation of Heteroaromatics

Published:2003-07-11 Issue:16 Volume:68 Page:6424-6426
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Ueno Makoto¹,Nabana Takahiro¹,Togo Hideo¹

Affiliation:

1. Graduate School of Science and Technology, and Department of Chemistry, Faculty of Science, Chiba University, Yayoi-cho 1-33, Inage-ku, Chiba 263-8522 Japan togo@scichem.s.chiba-u.ac.jp

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo030045t

Reference21 articles.

1. Hypervalent organoiodine. Crystal structure of phenylhydroxytosyloxyiodine

2. The reaction of 7-chloronorbornadiene with thallium cyclopentadienide. A convenient one-step synthesis of hexahydro-3,4,7-methenocyclopenta[a]pentalene

3. [ Hydroxy(tosyloxy)iodo]benzene, a versatile reagent for the mild oxidation of aryl iodides at the iodine atom by ligand transfer

4. One-step .alpha.-tosyloxylation of ketones with [hydroxy(tosyloxy)iodo]benzene

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