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^*

^*Korrespondierende*r Autor*in für diese Arbeit

Sygnature Discovery

Publikation: Beitrag in Fachzeitschrift › Artikel › Forschung › 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.

Originalsprache	Englisch
Seiten (von - bis)	8930-8933
Seitenumfang	4
Fachzeitschrift	Organic Letters
Jahrgang	21
Ausgabenummer	22
Elektronisch veröffentlicht (E-Pub)	30 Okt. 2019
DOIs	https://doi.org/10.1021/acs.orglett.9b03209
Publikationsstatus	Veröffentlicht - 15 Nov. 2019

ASJC Scopus Sachgebiete

Biochemie
Physikalische und Theoretische Chemie
Organische Chemie

Zugriff auf Dokument

10.1021/acs.orglett.9b03209

Andere Dateien und Links

Link zur Publikation in Scopus

Dieses zitieren

@article{f18b615b316e4d91b8dda4974d9773ff,

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.",

year = "2019",

month = nov,

day = "15",

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

language = "English",

volume = "21",

pages = "8930--8933",

journal = "Organic Letters",

issn = "1523-7060",

publisher = "American Chemical Society",

number = "22",

}

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

U2 - 10.1021/acs.orglett.9b03209

DO - 10.1021/acs.orglett.9b03209

M3 - Article

C2 - 31664844

AN - SCOPUS:85074728333

SN - 1523-7060

VL - 21

SP - 8930

EP - 8933

JO - Organic Letters

JF - Organic Letters

IS - 22

ER -