Toward Chromanes by de Novo Construction of the Benzene Ring

Egor Geist; Helge Berneaud-Kötz; Tomas Baikstis; Gerald Dräger; Andreas Kirschning

doi:10.1021/acs.orglett.9b03209

Toward Chromanes by de Novo Construction of the Benzene Ring

Egor Geist
, Helge Berneaud-Kötz
, Tomas Baikstis
, Gerald Dräger
, Andreas Kirschning^*

^*Corresponding author for this work

Sygnature Discovery

Research output: Contribution to journal › Article › Research › peer review

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.

Original language	English
Pages (from-to)	8930-8933
Number of pages	4
Journal	Organic Letters
Volume	21
Issue number	22
E-pub ahead of print	30 Oct 2019
DOIs	https://doi.org/10.1021/acs.orglett.9b03209
Publication status	Published - 15 Nov 2019

ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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10.1021/acs.orglett.9b03209

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title = "Toward Chromanes by de Novo Construction of the Benzene Ring",

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.",

author = "Egor Geist and Helge Berneaud-K{\"o}tz and Tomas Baikstis and Gerald Dr{\"a}ger and Andreas Kirschning",

note = "Funding Information: We thank Dr. J{\"o}rg Fohrer (Leibniz Universit{\"a} t Hannover, Hannover, Germany) for excellent support in the structural analysis of NMR spectroscopic data.",

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doi = "10.1021/acs.orglett.9b03209",

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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 - https://www.scopus.com/pages/publications/85074728333

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DO - 10.1021/acs.orglett.9b03209

M3 - Article

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AN - SCOPUS:85074728333

SN - 1523-7060

VL - 21

SP - 8930

EP - 8933

JO - Organic Letters

JF - Organic Letters

IS - 22

ER -

Toward Chromanes by de Novo Construction of the Benzene Ring

Abstract

ASJC Scopus subject areas

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