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An asymmetric synthesis of all stereoisomers of piclavines A1-4 using an iterative asymmetric dihydroxylation

Beilstein Journal of Organic Chemistry (2007) 3
DOI: 10.1186/1860-5397-3-37
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Abstract

The asymmetric synthesis of both enantiomers of piclavines A1, A2, A3, and A4 has been achieved using an iterative asymmetric dihydroxylation with enantiomeric enhancement. © 2007 Saito et al; licensee Beilstein-Institut.

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Saito, Y., Okamoto, N., & Takahata, H. (2007). An asymmetric synthesis of all stereoisomers of piclavines A1-4 using an iterative asymmetric dihydroxylation. Beilstein Journal of Organic Chemistry, 3. https://doi.org/10.1186/1860-5397-3-37

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