A practical entry to C18-constrained-E-ring analogues of methyllycaconitine (MLA): a concise new stereoselective approach to 8-oxa-decahydroisoquinolines accompanied by a simple microwaves-assisted synthesis of the succinimidobenzoate appendage of MLA-Reference-Cited by-同舟云学术

A practical entry to C18-constrained-E-ring analogues of methyllycaconitine (MLA): a concise new stereoselective approach to 8-oxa-decahydroisoquinolines accompanied by a simple microwaves-assisted synthesis of the succinimidobenzoate appendage of MLA

Published:2005-01 Issue:5 Volume:46 Page:759-762
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Simoni Daniele,Rossi Marcello,Rondanin Riccardo,Baruchello Riccardo,Grisolia Giuseppina,Eleopra Marco,Giovannini Riccardo,Bozzoli Andrea,Davalli Silvia,Di Fabio Romano,Donati Daniele

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference20 articles.

1. AN ALKALOID FROM DELPHINIUM BROWNII RYDB.

2. Diterpenoid and steroidal alkaloids

3. Methyllycaconitine: a selective probe for neuronal α-bungarotoxin binding sites

4. Exploring the Nature of Molecular Recognition in Nicotinic Acetylcholine Receptors

5. Preliminary Synthetic Studies of Methyllycaconitine, a Potent Nicotinic Acetylcholine Receptor Antagonist: Rapid Syntheses of AE-Bicyclic Analogues

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