STEREOSPECIFIC CYCLISATIONS OF SUBSTITUTED α'-LITHIATED α(Z),γ-BUTADIENYL SULFOXIDES

DOI: 10.1016/S0040-4039(00)98128-0

Source and publish data:

Tetrahedron Letters p. 2655 - 2658 (1985)

Update date:2022-07-29

Authors:

Reglier, Marius

Julia, Sylvestre A.

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Article abstract of DOI:10.1016/S0040-4039(00)98128-0

The title compounds 2(b-d) were prepared and converted stereospecifically to the lithiated derivatives of cyclic sulfoxides 3(b-d) through a proposed concerted disrotatory electrocyclisation.

Full text of DOI:10.1016/S0040-4039(00)98128-0

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Article Doi

STEREOSPECIFIC CYCLISATIONS OF SUBSTITUTED α'-LITHIATED α(Z),γ-BUTADIENYL SULFOXIDES

DOI: 10.1016/S0040-4039(00)98128-0

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4039(00)98128-0

Full text of DOI:10.1016/S0040-4039(00)98128-0

Products guided by the article

R&D Labs maybe for 100420-75-5

Relevant to this article

Stereoselective synthesis of β-methoxytyrosine derivatives for identification of the absolute configuration of callipeltin E

Luminescent gold(I) carbenes from 2-pyridylisocyanide complexes: Structural consequences of intramolecular versus intermolecular hydrogen-bonding interactions

Alkylzinc carboxylates as efficient precursors for zinc oxocarboxylates and sulfidocarboxylates

Transition-Metal-Free N-Arylation of Pyrazoles with Diaryliodonium Salts

Chemoselective and Diastereoconvergent Cu(II)-Catalyzed Aerobic Endoperoxidation of Polycarbonyls

A stable, convertible isonitrile as a formic acid carbanion [ -COOH] equivalent and its application in multicomponent reactions

A stable, convertible isonitrile as a formic acid carbanion [ ^-COOH] equivalent and its application in multicomponent reactions