Enantiospecific synthesis of angular triquinanes
| Data(s) |
31/07/2011
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|---|---|
| Resumo |
The enantiospecific synthesis of angular triquinanes has been developed starting from the readily available (S)-campholenaldehyde. Two alternate strategies have been used, one employing a Johnson's orthoester Claisen rearrangement followed by an intramolecular cyclopropanation and regioselective cyclopropane ring cleavage, and a second one based on a RCM reaction. (C) 2011 Elsevier Ltd. All rights reserved. |
| Formato |
application/pdf |
| Identificador |
http://eprints.iisc.ernet.in/42852/1/Enantiospecific.pdf Srikrishna, Adusumilli and Gowni, Vijayendran (2011) Enantiospecific synthesis of angular triquinanes. In: Tetrahedron: Asymmetry, 22 (14-15). pp. 1553-1559. |
| Publicador |
Elsevier Science |
| Relação |
http://dx.doi.org/10.1016/j.tetasy.2011.08.016 http://eprints.iisc.ernet.in/42852/ |
| Palavras-Chave | #Organic Chemistry |
| Tipo |
Journal Article PeerReviewed |
