## Synthesis of a Hybrid Analogue of the Esperamicin and Dynemicin Cores. -The compound (VI) represents an enediyne analogue hybrid of the core structures of esperamicin and dynemicin. Key step in the sequence is the intramolecular Reissert-type reaction of the anion of the Z-1,3-diyn-2-ene (III)
โฆ LIBER โฆ
ChemInform Abstract: Synthesis of an Esperamicin Core Analogue with an Epoxide Trigger.
โ Scribed by H. MASTALERZ; T. W. DOYLE; J. F. KADOW; D. M. VYAS
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 29 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
ChemInform Abstract: Synthesis of a Hybr
โ
H. MASTALERZ; T. W. DOYLE; J. F. KADOW; D. M. VYAS
๐
Article
๐
2010
๐
John Wiley and Sons
โ 31 KB
๐ 2 views
ChemInform Abstract: Synthesis of an Unn
โ
Ivan R. Green; Felismino E. Tocoli
๐
Article
๐
2010
๐
John Wiley and Sons
โ 32 KB
๐ 2 views
ChemInform Abstract: Synthesis of an Epo
โ
F. FERRI; R. BRUECKNER
๐
Article
๐
2010
๐
John Wiley and Sons
โ 27 KB
๐ 2 views
ChemInform Abstract: Synthesis of an 1โฒ-
โ
Vinni Andreassen; Birte Svensson; Mikael Bols
๐
Article
๐
2010
๐
John Wiley and Sons
โ 27 KB
๐ 2 views
ChemInform Abstract: Enantioselective Sy
โ
Margaret A. Brimble; Prabhakar Bachu; Jonathan Sperry
๐
Article
๐
2008
๐
John Wiley and Sons
โ 16 KB
๐ 2 views
ChemInform Abstract: An Epoxide Rearrang
โ
David M. Hodgson; Christopher R. Maxwell; Ian R. Matthews
๐
Article
๐
2010
๐
John Wiley and Sons
โ 31 KB
๐ 1 views
An Epoxide Rearrangement -Radical Rearrangement Approach to 6-Substituted 2-Azabicyclo[2.2.1]-5-heptenes: Synthesis of an Epibatidine Analogue. -Base-promoted isomerization of the epoxide (I) provides the azanortricyclanol (II). The latter can be readily converted to the derivatives (V) as precurso