A MILD PROCEDURE FOR HYDROLYSIS OF ALKOXYMETHYL ARYL ETHERS TO GIVE HYDROXYARENES. A RATIONAL SYNTHESIS OF ASCOFURANONE

DOI: 10.1016/S0040-4039(00)84326-9

Source and publish data:

Tetrahedron Letters p. 1607 - 1610 (1986)

Update date:2022-08-10

Topics:

Authors:

Saimoto, Hiroyuki

Kusano, Yukari

Hiyama, Tamejiro

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1016/S0040-4039(00)84326-9

A mild procedure is reported for cleavage of alkoxymethyl aryl ethers with P₂I₄ to afford hydroxyarenes, and this deprotection method was successfully applied to the synthesis of an antibiotic ascofuranone through a rational approach.

Full text of DOI:10.1016/S0040-4039(00)84326-9

Products guided by the article

Product name:4-Nitrophenol

Cas No:100-02-7

Relevant to this article

Erratum: N-tosyl- S -difluoromethyl- S -phenylsulfoximine: A new difluoromethylation reagent for S-, N-, and C-nucleophiles (Organic Letters (2111))

Doi:10.1021/ol402896j
(2013)
Hydrogenation of toluene over La_0.8Sr_0.2Fe_1-x Co_xO_3-zz perovskite catalysts

Doi:10.1515/znb-1997-0807
(1997)
Doi:10.1039/P19730000626
(1973)
Synthesis of novel fluorophenylpyrazole-picolinamide derivatives and determination of their anticancer activity

Doi:10.1080/00397911.2020.1791341
(2020)
Unusual reaction of trifluorophenylsilane with dimethyl sulfoxide

Doi:10.1023/A:1012337030680
(2001)
Synthesis and potassium channel opening activity of substituted 10H-benzo[4,5]furo[3,2-b]indole- and 5,10-dihydro-indeno[1,2-b]indole-1-carboxylic acids

Doi:10.1016/S0960-894X(01)00385-7
(2001)

Article Doi

A MILD PROCEDURE FOR HYDROLYSIS OF ALKOXYMETHYL ARYL ETHERS TO GIVE HYDROXYARENES. A RATIONAL SYNTHESIS OF ASCOFURANONE

DOI: 10.1016/S0040-4039(00)84326-9

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4039(00)84326-9

Full text of DOI:10.1016/S0040-4039(00)84326-9

Products guided by the article

Relevant to this article

Hot Product