Details
| Original language | English |
|---|---|
| Pages (from-to) | 8930-8933 |
| Number of pages | 4 |
| Journal | Organic Letters |
| Volume | 21 |
| Issue number | 22 |
| Early online date | 30 Oct 2019 |
| Publication status | Published - 15 Nov 2019 |
Abstract
The work describes three principal Diels-Alder cycloaddition approaches toward chromanes that are designed for the de novo construction of the benzene ring. This study specifically focuses on the potential exploitation in the total synthesis of chromane-bearing natural products such as cebulactam A.
ASJC Scopus subject areas
- Biochemistry, Genetics and Molecular Biology(all)
- Biochemistry
- Chemistry(all)
- Physical and Theoretical Chemistry
- Chemistry(all)
- Organic Chemistry
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In: Organic Letters, Vol. 21, No. 22, 15.11.2019, p. 8930-8933.
Research output: Contribution to journal › Article › Research › peer review
}
TY - JOUR
T1 - Toward Chromanes by de Novo Construction of the Benzene Ring
AU - Geist, Egor
AU - Berneaud-Kötz, Helge
AU - Baikstis, Tomas
AU - Dräger, Gerald
AU - Kirschning, Andreas
N1 - Funding Information: We thank Dr. Jörg Fohrer (Leibniz Universitä t Hannover, Hannover, Germany) for excellent support in the structural analysis of NMR spectroscopic data.
PY - 2019/11/15
Y1 - 2019/11/15
N2 - The work describes three principal Diels-Alder cycloaddition approaches toward chromanes that are designed for the de novo construction of the benzene ring. This study specifically focuses on the potential exploitation in the total synthesis of chromane-bearing natural products such as cebulactam A.
AB - The work describes three principal Diels-Alder cycloaddition approaches toward chromanes that are designed for the de novo construction of the benzene ring. This study specifically focuses on the potential exploitation in the total synthesis of chromane-bearing natural products such as cebulactam A.
UR - http://www.scopus.com/inward/record.url?scp=85074728333&partnerID=8YFLogxK
U2 - 10.1021/acs.orglett.9b03209
DO - 10.1021/acs.orglett.9b03209
M3 - Article
C2 - 31664844
AN - SCOPUS:85074728333
VL - 21
SP - 8930
EP - 8933
JO - Organic Letters
JF - Organic Letters
SN - 1523-7060
IS - 22
ER -