Trapping of a phosphazide intermediate in the Staudinger reaction of tertiary phosphines with azides and its application to the synthesis of analogs of the marine alkaloid midpacamide-Reference-Cited by-同舟云学术

Trapping of a phosphazide intermediate in the Staudinger reaction of tertiary phosphines with azides and its application to the synthesis of analogs of the marine alkaloid midpacamide

Published:2004-02 Issue:8 Volume:45 Page:1655-1657
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Fresneda Pilar M.,Castañeda Marta,Sanz Miguel A.,Molina Pedro

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference32 articles.

1. Recent advances in the staudinger reaction

2. Unexpected Staudinger reaction of α-azidoacetonitriles α-phenyl substituted with triphenylphosphine. Preparation, X-ray crystal and molecular structures of a phosphazine, an aminophosphonium carbanion salt and a phosphazide, with (Z)-configuration

3. New Cage Compounds: Preparation and Characterization of ChiralC3-Symmetric Macrobicyclic Tris(phosphazides)

4. Isolation, Reactivity and Intramolecular Trapping of Phosphazide Intermediates in the Staudinger Reaction of Tertiary Phosphines with Azides

5. Intramolecular trapping of a phosphazide by an imine: Formation of 2,3-diamino-2H-indazole derivatives from o-azidobenzaldimines and tertiary phosphines

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