Stereospecific nitromethane coniugate addition to 4-oxygenated-2-substituted cyclopent-2-enones: A simple approach to prostaglandins.

P. . G. . BARALDI; A. . BARCO; BENETTI, Simonetta; G. . P. . POLLINI; D. . SIMONI; V. . ZANIRATO

oai:iris.unife.it:11392/460284

Stereospecific nitromethane coniugate addition to 4-oxygenated-2-substituted cyclopent-2-enones: A simple approach to prostaglandins.

Authors: P. . G. . BARALDI
A. . BARCO
Simonetta BENETTI
G. . P. . POLLINI
D. . SIMONI
V. . ZANIRATO
Publication date: 1 January 1987
Publisher

Abstract

The compatibility of nitromethane conjugate addition to 2-cyclopentenones bearing a 4-oxygenated funtion has been illustrated trough a short and proctical sunthesis of Corey aldehyde. A new synthesis of PGF2a featuring the introduction of the omega-chain via [3+2] cycloaddition has been described

info:eu-repo/semantics/article

Similar works

Full text

Archivio istituzionale della ricerca - Università di Ferrara

oai:iris.unife.it:11392/460284

Last time updated on 12/11/2016

This paper was published in Archivio istituzionale della ricerca - Università di Ferrara.

Having an issue?

Is data on this page outdated, violates copyrights or anything else? Report the problem now and we will take corresponding actions after reviewing your request.