Stereospecificity in Intramolecular Photoredox Reactions of Naphthoquinones: Enantioselective Total Synthesis of (-)-SpiroxinC
Intramolecular photoredox reactions of naphthoquinone derivatives were found to proceed in a stereospecific manner. This method was used as a basis for the enantioselective total synthesis of (-)-spiroxinC.
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| Published in | Angewandte Chemie Vol. 129; no. 38; p. 11618 |
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| Main Authors | , , , , |
| Format | Journal Article |
| Language | German |
| Published |
Weinheim
Wiley Subscription Services, Inc
11.09.2017
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| Subjects | |
| Online Access | Get full text |
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| Abstract | Intramolecular photoredox reactions of naphthoquinone derivatives were found to proceed in a stereospecific manner. This method was used as a basis for the enantioselective total synthesis of (-)-spiroxinC. |
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| AbstractList | Intramolecular photoredox reactions of naphthoquinone derivatives were found to proceed in a stereospecific manner. This method was used as a basis for the enantioselective total synthesis of (-)-spiroxinC. |
| Author | Hanaki, Atsuko Ohmori, Ken Ando, Yoshio Suzuki, Keisuke Sasaki, Ryota |
| Author_xml | – sequence: 1 givenname: Yoshio surname: Ando fullname: Ando, Yoshio – sequence: 2 givenname: Atsuko surname: Hanaki fullname: Hanaki, Atsuko – sequence: 3 givenname: Ryota surname: Sasaki fullname: Sasaki, Ryota – sequence: 4 givenname: Ken surname: Ohmori fullname: Ohmori, Ken – sequence: 5 givenname: Keisuke surname: Suzuki fullname: Suzuki, Keisuke |
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| DOI | 10.1002/ange.201705562 |
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| Snippet | Intramolecular photoredox reactions of naphthoquinone derivatives were found to proceed in a stereospecific manner. This method was used as a basis for the... |
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| Title | Stereospecificity in Intramolecular Photoredox Reactions of Naphthoquinones: Enantioselective Total Synthesis of (-)-SpiroxinC |
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