Get all the updates for this publication
Letters
Synthetic approaches to komarovispiranes. Enantiospecific synthesis of bicyclo[3.3.0]octanespiro[3.1′]cyclohexanesPublished in Elsevier BV
2007
Volume: 48
Issue: 13
Pages: 2291 - 2294
A ring-closing metathesis based spiroannulation of cyclopentane and cyclohexanes at the C-3 carbon atom of a bicyclo[3.3.0]octane, as a model study directed towards the enantiospecific synthesis of the novel diterpenes komarovispiranes, is described.
Content may be subject to copyright.
About the journal
| Journal | Data powered by TypesetTetrahedron Letters |
|---|---|
| Publisher | Data powered by TypesetElsevier BV |
| Open Access | No |
Authors (1)
Beeraiah Baire- Ag(I)-Catalyzed Cyclizative Hydration of Alkynes and Propargylic Alcohols. A Mild Approach to 2-Acylfuran Derivatives
- Intercepted Meyer–Schuster Rearrangements in Organic Synthesis
- Formal Halo-Meyer-Schuster Rearrangement of Propargylic Acetates through a Novel Intermediate and an Unexampled Mechanistic Pathway
- Mild Approach to 2-Acylfurans via Intercepted Meyer-Schuster Rearrangement of 6-Hydroxyhex-2-en-4-ynals
