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Stereoselective Addition of Organocopper Reagents to Cyclic N-Acyliminium Ions.

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This article is published in Acta Chemica Scandinavica.The article was published on 1994-01-01 and is currently open access. It has received 21 citations till now.

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Synthesis of bridged azabicyclic structures via ring-closing olefin metathesis.

TL;DR: A new strategy for the facile synthesis of azabicyclo[m.n.1]alkenes has been developed that involves the ring-closing metathesis (RCM) reaction of cis-2,6-dialkenyl-N-acyl piperidine derivatives, which may serve as a useful intermediate in syntheses of several Sarpagine alkaloids.
Journal ArticleDOI

Synthesis of functionally diverse bicyclic sulfonamides as constrained proline analogues and application to the design of potential thrombin inhibitors

TL;DR: A sulfonamide counterpart of an indolizidinone 2-carboxylic acid was synthesized and evaluated for its activity against the enzyme thrombin.
Journal ArticleDOI

Rhodium-Catalyzed Cyclohydrocarbonylation: Application to the Synthesis of (+)-Prosopinine and (−)-Deoxoprosophylline†

TL;DR: These two short total syntheses clearly demonstrate the usefulness of the extremely regioselective cyclohydrocarbonylation process developed in these laboratories for the concise syntheses of piperidine alkaloids and related compounds.
Journal ArticleDOI

Stereocontrolled total synthesis of (--)-kaitocephalin.

TL;DR: This paper describes the successful implementation of a stereocontrolled strategy for the total chemical synthesis of the pyrrolidine-based alkaloid (--)-kaitocephalin that profits from the strategic utilization of substrate-controlled manipulations for the iterative installation of the requisite stereogenic centers.
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