Conformational dependent regio- and stereo-selectivity in transformations of germacrenes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference26 articles.
1. Conformational dependence in the photochemistry of (E,E )-germacra-1(10),4,7(11)-triene
2. Conformational isomerism in dihydropregeijerene and hedycaryol
3. Regio- and stereo-specificity in the cyclisation of medium ring 1,5-dienes
4. Stereochemical implications in sesquiterpene biogenesis
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1. Photochemistry of 4,5-dihydro-8-hydroxygermacrene B;Recueil des Travaux Chimiques des Pays-Bas;2010-09-02
2. Thermal reactions of endo- and exo-6-methylbicyclo[3.2.0]hept-2-enes: an experimental test for a potential ring inversion;Tetrahedron Letters;2001-01
3. The synthesis of germacrane sesquiterpenes and related compounds;Tetrahedron;1999-02
4. About the Chiral Stability of Germacrene B and the Biomimetic Synthesis of Guaiane Sesquiterpenes;The Journal of Organic Chemistry;1997-10-01
5. Acid cyclization of 5-ketogermacren-6,12-olides. A reactivity and conformational study;Tetrahedron;1996-09
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