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

The asymmetric synthesis of both enantiomers of piclavines A1, A2, A3, and A4 has been achieved using an iterative asymmetric dihydroxylation with enantiomeric enhancement.

Detalles Bibliográficos
Autores principales: Saito, Yukako, Okamoto, Naoki, Takahata, Hiroki
Formato: Texto
Lenguaje:English
Publicado: Beilstein-Institut 2007
Materias:
Full Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2200665/
https://www.ncbi.nlm.nih.gov/pubmed/17967195
http://dx.doi.org/10.1186/1860-5397-3-37
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author Saito, Yukako
Okamoto, Naoki
Takahata, Hiroki
author_facet Saito, Yukako
Okamoto, Naoki
Takahata, Hiroki
author_sort Saito, Yukako
collection PubMed
description The asymmetric synthesis of both enantiomers of piclavines A1, A2, A3, and A4 has been achieved using an iterative asymmetric dihydroxylation with enantiomeric enhancement.
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spelling pubmed-22006652008-01-16 An asymmetric synthesis of all stereoisomers of piclavines A1-4 using an iterative asymmetric dihydroxylation Saito, Yukako Okamoto, Naoki Takahata, Hiroki Beilstein J Org Chem Full Research Paper The asymmetric synthesis of both enantiomers of piclavines A1, A2, A3, and A4 has been achieved using an iterative asymmetric dihydroxylation with enantiomeric enhancement. Beilstein-Institut 2007-10-29 /pmc/articles/PMC2200665/ /pubmed/17967195 http://dx.doi.org/10.1186/1860-5397-3-37 Text en Copyright © 2007, Saito et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Saito, Yukako
Okamoto, Naoki
Takahata, Hiroki
An asymmetric synthesis of all stereoisomers of piclavines A1-4 using an iterative asymmetric dihydroxylation
title An asymmetric synthesis of all stereoisomers of piclavines A1-4 using an iterative asymmetric dihydroxylation
title_full An asymmetric synthesis of all stereoisomers of piclavines A1-4 using an iterative asymmetric dihydroxylation
title_fullStr An asymmetric synthesis of all stereoisomers of piclavines A1-4 using an iterative asymmetric dihydroxylation
title_full_unstemmed An asymmetric synthesis of all stereoisomers of piclavines A1-4 using an iterative asymmetric dihydroxylation
title_short An asymmetric synthesis of all stereoisomers of piclavines A1-4 using an iterative asymmetric dihydroxylation
title_sort asymmetric synthesis of all stereoisomers of piclavines a1-4 using an iterative asymmetric dihydroxylation
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2200665/
https://www.ncbi.nlm.nih.gov/pubmed/17967195
http://dx.doi.org/10.1186/1860-5397-3-37
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