Generation of β-carboline azomethine ylides via trimethylsilylmethyl trifluoromethane sulfonate quaternisations: Entry into the new class of 11H-indolizino[8,7-b]indole heterocycles-Reference-Cited by-同舟云学术

Generation of β-carboline azomethine ylides via trimethylsilylmethyl trifluoromethane sulfonate quaternisations: Entry into the new class of 11H-indolizino[8,7-b]indole heterocycles

Published:1989-01 Issue:26 Volume:30 Page:3423-3426
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Poissonnet Guillaume,Potier Pierre,Dodd Robert H.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference7 articles.

1. Three Alkaloids as Selective Destroyers of Cancer Cells in Mice

2. Ylides by the desilylation of .alpha.-silyl onium salts

3. N-(TRIMETHYLSILYLMETHYL) PYRIDINIUM TRIFLUOROMETHANESULFONATES AS FACILE PRECURSORS FOR NONSTABIL1ZED PYRID1NIUM METHYLIDES

4. Generation of azomethine ylides via the desilylation reaction of immonium salts

5. Urinary and brain beta-carboline-3-carboxylates as potent inhibitors of brain benzodiazepine receptors.

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1. Azomethine Ylides in Organic Synthesis;Current Organic Chemistry;2003-07-01

2. Cytotoxic activities of novel hexahydroindolizino[8,7-b]indole derivatives prepared by 1,3-dipolar cycloaddition reactions of 3,4-dihydro-β-carboline ylides;Bioorganic & Medicinal Chemistry;2001-08

3. New entries into theindolizino[8,7-b]indole ring system;Tetrahedron;1999-08

4. Synthesis of some indolylpyrroles and indolylpyrrolylketones;Tetrahedron;1997-06

5. Preparation and 1,3-Dipolar Cycloaddition Reactions of β-Carboline Azomethine Ylides: A Direct Entry into C-1- and/or C-2-Functionalized Indolizino[8,7-b]indole Derivatives;The Journal of Organic Chemistry;1996-01-01