Selective deprotection of propargyl ethers using tetrathiomolybdate

DOI: 10.1055/s-1997-6132

Source and publish data:

Synlett p. 513 - 514 (1997)

Update date:2022-08-30

Topics:

Authors:

Swamy Swamy

Ilankumaran, Palanichamy

Chandrasekaran, Srinivasan

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

Article abstract of DOI:10.1055/s-1997-6132

Benzyltriethylammonium tetrathiomolybdate, [PhCH₂NEt₃]₂MoS₄, 1 deprotects propargyl ethers of alcohols and phenols in a selective manner in high yields. Easily reducible groups like nitro, aldehyde, keto and allyl are not affected.

Full text of DOI:10.1055/s-1997-6132

Products guided by the article

Product name:4-Nitrophenol

Cas No:100-02-7

Relevant to this article

Magnetically separable carbon nanocomposite catalysts for efficient nitroarene reduction and Suzuki reactions

Doi:10.1016/j.apcata.2014.02.029
(2014)
Doi:10.1007/BF00569584
()
Electroreductive coupling of organic halides with aldehydes catalyzed by nickel(0) complex with 2,2′-bipyridine

Doi:10.1023/A:1012381707114
(2001)
Control of the catalytic effect of cetyltrimethylammonium bromide micelles by the addition of background electrolyte and nonionic surfactant

Doi:10.1007/s11172-007-0312-9
(2007)
Synthesis of ¹⁸O-labeled photosynthetically active chlorophylls at the 3- or 7-carbonyl group with high regioselectivity

Doi:10.1007/s11120-010-9590-4
(2010)
Vibrational Spectroscopic Characterization of Glycerol Reaction Pathways over Metal-Modified Molybdenum Carbide Surfaces

Doi:10.1002/cctc.201901629
(2020)

Article Doi

Selective deprotection of propargyl ethers using tetrathiomolybdate

DOI: 10.1055/s-1997-6132

Source and publish data:

Authors:

Article abstract of DOI:10.1055/s-1997-6132

Full text of DOI:10.1055/s-1997-6132

Products guided by the article

Relevant to this article

Hot Product