Controlling 6-endo-selectivity in oxidation/bromocyclization cascades for synthesis of aplysiapyranoids and other 2,2,6,6-substituted tetrahydropyrans-Reference-Cited by-同舟云学术

Controlling 6-endo-selectivity in oxidation/bromocyclization cascades for synthesis of aplysiapyranoids and other 2,2,6,6-substituted tetrahydropyrans

Published:2012-08 Issue:34 Volume:68 Page:6968-6980
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Brücher Oliver,Bergsträßer Uwe,Kelm Harald,Hartung Jens,Greb Marco,Svoboda Ingrid,Fuess Hartmut

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference60 articles.

1. Novel cytotoxic monoterpenes having a halogenated tetrahydropyran from Aplysia kurodai

2. Structure and absolute configuration of aplysiapyranoid B, a new polyhalogenated pyranoid monoterpene from Aplysia kurodai

3. Efficient total synthesis of the cytotoxic halogenated monoterpene aplysiapyranoid A

4. Total Syntheses of the Cytotoxic Marine Natural Product, Aplysiapyranoid C1

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