A versatile regio- and stereospecific annulation method - II-Reference-Cited by-同舟云学术

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A versatile regio- and stereospecific annulation method - II

Published:1989-01 Issue:5 Volume:45 Page:1391-1408
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Böhm Karin,Gössinger Edda,Müller Renate

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference32 articles.

1. Gössinger, E., Müller, R. preceding publication.

2. Stereoelectronic effects on acetal hydrolysis

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1. Towards EPC-syntheses of the structural class of cochleamycins and macquarimicins. Part 2: EPC-synthesis of the hydrindene subunit of the macquarimicins;Tetrahedron;2007-08

2. Towards EPC-syntheses of the structural class of cochleamycins and macquarimicins. Part 1: EPC-synthesis of the hydrindene subunit of the cochleamycins;Tetrahedron;2007-08

3. A simple entry into enantiopure hydrindanes, hydroisoquinolones and diquinanes from 3,10-dioxygenated dicyclopentadienes: Application to the synthesis of (+)-coronafacic acid and a formal synthesis of (+)-coriolin;Journal of the Chemical Society, Perkin Transactions 1;2001

4. Total synthesis of chatancin;ANGEW CHEM INT EDIT;1998

5. Totalsynthese von Chatancin;Angewandte Chemie;1998-08-17

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