Diastereoselective synthesis of chiral thiiranes by 1,3-dipolar cycloaddition of imidazo[2,1-b]thiazolium-4-olate systems with aromatic aldehydes

DOI: 10.1016/S0040-4039(00)60505-1

Source and publish data:

Tetrahedron Letters p. 2999 - 3002 (1993)

Update date:2022-08-03

Topics:

Authors:

Areces, Pilar

Avalos, Martin

Babiano, Reyes

Gonzalez, Luis

Jimenez, Jose L.

Mendez, Maria M.

Palacios, Juan C.

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Article abstract of DOI:10.1016/S0040-4039(00)60505-1

The regiospecific and diastereoselective 1,3-dipolar cycloaddition of imidazo[1,2-b]thiazolium-4-olate systems with aromatic aldehydes gives thiiranes, which undergo thermal decomposition to olefins.

Full text of DOI:10.1016/S0040-4039(00)60505-1

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Article Doi

Diastereoselective synthesis of chiral thiiranes by 1,3-dipolar cycloaddition of imidazo[2,1-b]thiazolium-4-olate systems with aromatic aldehydes

DOI: 10.1016/S0040-4039(00)60505-1

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4039(00)60505-1

Full text of DOI:10.1016/S0040-4039(00)60505-1

Products guided by the article

R&D Labs maybe for 150928-59-9

Relevant to this article

Synthesis and conformational characterization of diketopiperazines bearing a benzyl moiety

Regiocontrolled ring opening of monoprotected 2,3-epoxy-1,4-diols by using alkynyl aluminum reagents: Synthesis of differentially monoprotected alkynyl triol derivatives

Cooperative catalysis of p-aminophenol and titanocene dichloride in direct Mannich reactions with acetone

Organocopper(III) spiro complexes: Synthesis, structural characterization, and redox transformation

Sequence peptide polymers. 3. Poly Asp(OH)-Ser(H)-Gly and other serine-containing polymers.

A facile preparation method for α,α-difluoroalkanecarboxylic acids and esters. A formal difluoromethylene insertion to alkanecarboxylic acids using radical reaction