Asymmetric Synthesis Utilizing Circularly Polarized Light Mediated by the Photoequilibrium of Chiral Olefins in Conjunction with Asymmetric Autocatalysis

The light touch: Asymmetric photoequilibrium and autocatalysis act as sources of homochirality in a highly enantioselective preparation of chiral alcohols (see scheme). This process is initiated by left‐ and right‐circularly polarized light (CPL) and exploits the resulting photoequilibrium between c...

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Veröffentlicht in:Angewandte Chemie International Edition 2004-08, Vol.43 (34), p.4490-4492
Hauptverfasser: Sato, Itaru, Sugie, Rie, Matsueda, Yohei, Furumura, Yuri, Soai, Kenso
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container_issue 34
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container_title Angewandte Chemie International Edition
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creator Sato, Itaru
Sugie, Rie
Matsueda, Yohei
Furumura, Yuri
Soai, Kenso
description The light touch: Asymmetric photoequilibrium and autocatalysis act as sources of homochirality in a highly enantioselective preparation of chiral alcohols (see scheme). This process is initiated by left‐ and right‐circularly polarized light (CPL) and exploits the resulting photoequilibrium between chiral olefin substrates to yield 2‐alkynyl‐5‐pyrimidyl alkanols.
doi_str_mv 10.1002/anie.200454162
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source Wiley Online Library Journals Frontfile Complete
subjects alkenes
asymmetric amplification
asymmetric catalysis
autocatalysis
chirality
title Asymmetric Synthesis Utilizing Circularly Polarized Light Mediated by the Photoequilibrium of Chiral Olefins in Conjunction with Asymmetric Autocatalysis
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