Oxidation of dihydropyran with MoO5·HMPA

Aryeh A. Frimer

doi:10.1039/C39770000205

Oxidation of dihydropyran with MoO₅·HMPA

Aryeh A. Frimer

Department of Chemistry

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

12 Scopus citations

Abstract

The reaction of dihydropyran with MoO₅·HMPA yields C-formyloxybutanal, in inert solvents; in methanol, however, the solvolysis products of the epoxide of dihydropyran are obtained.

Original language	English
Pages (from-to)	205-206
Number of pages	2
Journal	Chemical Communications
Issue number	7
DOIs	https://doi.org/10.1039/C39770000205
State	Published - 1977

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title = "Oxidation of dihydropyran with MoO5·HMPA",

abstract = "The reaction of dihydropyran with MoO5·HMPA yields C-formyloxybutanal, in inert solvents; in methanol, however, the solvolysis products of the epoxide of dihydropyran are obtained.",

author = "Frimer, {Aryeh A.}",

year = "1977",

doi = "10.1039/C39770000205",

language = "אנגלית",

pages = "205--206",

journal = "Chemical Communications",

issn = "0022-4936",

publisher = "Royal Society of Chemistry",

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AU - Frimer, Aryeh A.

PY - 1977

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N2 - The reaction of dihydropyran with MoO5·HMPA yields C-formyloxybutanal, in inert solvents; in methanol, however, the solvolysis products of the epoxide of dihydropyran are obtained.

AB - The reaction of dihydropyran with MoO5·HMPA yields C-formyloxybutanal, in inert solvents; in methanol, however, the solvolysis products of the epoxide of dihydropyran are obtained.

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JO - Chemical Communications

JF - Chemical Communications

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Oxidation of dihydropyran with MoO₅·HMPA

Abstract

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