Stereoselective synthesis of 3,4-disubstituted tetrahydrofurans and 2,3,4-trisubstituted tetrahydrofurans using an intramolecular allylation strategy employing allylsilanes-Reference-Cited by-同舟云学术

Stereoselective synthesis of 3,4-disubstituted tetrahydrofurans and 2,3,4-trisubstituted tetrahydrofurans using an intramolecular allylation strategy employing allylsilanes

Published:2008-04 Issue:16 Volume:49 Page:2514-2518
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Jervis Peter J.,Kariuki Benson M.,Cox Liam R.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference28 articles.

1. Enantioselective Synthesis of C(8)-Hydroxylated Lignans—Early Approaches and Recent Advances

2. Annonaceous Acetogenins - Synthetic Approaches Towards a Novel Class of Natural Products

3. Pachastrissamine, a Cytotoxic Anhydrophytosphingosine from a Marine Sponge, Pachastrissa sp.

4. Jaspines A and B: two new cytotoxic sphingosine derivatives from the marine sponge Jaspis sp.

5. Stereoselective total synthesis of pachastrissamine (jaspine B)

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