Intramolecular Cycloadditions of Keteniminium Salts. A Practical Asymmetric Synthesis of Prostaglandins

DOI: 10.1016/S0957-4166(00)80017-8

Source and publish data:

Tetrahedron Asymmetry p. 1181 - 1184 (1991)

Update date:2022-07-29

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Authors:

Chen, Lian-yong

Ghosez, Leon

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Article abstract of DOI:10.1016/S0957-4166(00)80017-8

The intramolecular <2 + 2> cycloaddition of keteniminium salt 5 derived from (2S,5S)-dimethylpyrrolidine is the key step of a short synthetic route toward prostaglandins.

Full text of DOI:10.1016/S0957-4166(00)80017-8

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Article Doi

Intramolecular Cycloadditions of Keteniminium Salts. A Practical Asymmetric Synthesis of Prostaglandins

DOI: 10.1016/S0957-4166(00)80017-8

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0957-4166(00)80017-8

Full text of DOI:10.1016/S0957-4166(00)80017-8

Products guided by the article

R&D Labs maybe for 139108-46-6

Relevant to this article

Metal-free arylation of pyrimidines through a photochemical process

Photoinduced energy and electron transfer in phenylethynyl-bridged zinc porphyrin-oligothienylenevinylene-C60 ensembles

Enantioselective construction of 3-hydroxy oxindoles via decarboxylative addition of β-ketoacids to isatins

Alumina-Catalyzed Addition of Thiols to Methyl Propiolate

A photochromic ATP analogue driving a motor protein with reversible light-controlled motility: Controlling velocity and binding manner of a kinesin-microtubule system in an in vitro motility assay

Tunneling rearrangement of 1-azulenylcarbene

Photoinduced energy and electron transfer in phenylethynyl-bridged zinc porphyrin-oligothienylenevinylene-C₆₀ ensembles