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Diastereoselection in the Formation of Spirocyclic Oxindoles by the Intramolecular Heck Reaction
Diastereoselective double Heck cyclizations of cyclohexene diamides 1 and 3 form contiguous quaternary stereocenters, with diastereoselection being controlled by the trans diol-protecting group. In this, the first in a series of two papers, the origin of diastereoselection in the first ring closure...
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| Autori principali: | , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2006
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2585599/ https://ncbi.nlm.nih.gov/pubmed/16555809 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/jo052335a |
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