Total synthesis and absolute stereochemistry of (+)-batzellaside B and its C8-epimer, a new class of piperidine alkaloids from the sponge Batzella sp.-Reference-Cited by-同舟云学术

Total synthesis and absolute stereochemistry of (+)-batzellaside B and its C8-epimer, a new class of piperidine alkaloids from the sponge Batzella sp.

Published:2011-03 Issue:11 Volume:52 Page:1173-1175
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Wierzejska Jolanta,Ohshima Manami,Inuzuka Toshiyasu,Sengoku Tetsuya,Takahashi Masaki,Yoda Hidemi

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference17 articles.

1. A Madagascar Sponge Batzella sp. as a Source of Alkylated Iminosugars

2. Syntheses with Partially Benzylated Sugars. II.1 The Anomeric 1-O-Benzoyl-L-arabinopyranoses and 1-O-Benzoyl-L-arabinofuranoses and Their Tendencies to Undergo Acyl Migration

3. Asymmetric total synthesis of natural pyrrolizidine alkaloid, (+)-alexine

4. A new procedure for the synthesis of azasugars

5. An efficient asymmetric functionalization to highly substituted pyrrolidines

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