Exploring Heterotropones and Examining Their Propensity to Undergo [4 + 2] Cycloadditions

Casper Larsen Barløse; Jonas Faghtmann; Mikk Kaasik; Roberta Mastroddi; Karl Anker Jørgensen

doi:10.1021/acs.orglett.3c04080

Exploring Heterotropones and Examining Their Propensity to Undergo [4 + 2] Cycloadditions

Casper Larsen Barløse, Jonas Faghtmann, Mikk Kaasik, Roberta Mastroddi, Karl Anker Jørgensen^*

^*Corresponding author af dette arbejde

Institut for Kemi

Publikation: Bidrag til tidsskrift/Konferencebidrag i tidsskrift /Bidrag til avis › Letter › peer review

Abstract

An efficient strategy to obtain a broad array of chiral and achiral heterotropones and their corresponding [4 + 2] cycloadducts is disclosed. This strategy enables access to unique heterotropones and intricate bicyclic structures in high yields and diastereoselectivities through a simple procedure and from easily accessible starting materials.

Originalsprog	Engelsk
Tidsskrift	Organic Letters
Vol/bind	26
Nummer	8
Sider (fra-til)	1539-1543
Antal sider	5
ISSN	1523-7060
DOI	https://doi.org/10.1021/acs.orglett.3c04080
Status	Udgivet - mar. 2024

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10.1021/acs.orglett.3c04080

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title = "Exploring Heterotropones and Examining Their Propensity to Undergo [4 + 2] Cycloadditions",

abstract = "An efficient strategy to obtain a broad array of chiral and achiral heterotropones and their corresponding [4 + 2] cycloadducts is disclosed. This strategy enables access to unique heterotropones and intricate bicyclic structures in high yields and diastereoselectivities through a simple procedure and from easily accessible starting materials.",

author = "Barl{\o}se, {Casper Larsen} and Jonas Faghtmann and Mikk Kaasik and Roberta Mastroddi and J{\o}rgensen, {Karl Anker}",

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T1 - Exploring Heterotropones and Examining Their Propensity to Undergo [4 + 2] Cycloadditions

AU - Barløse, Casper Larsen

AU - Faghtmann, Jonas

AU - Kaasik, Mikk

AU - Mastroddi, Roberta

AU - Jørgensen, Karl Anker

PY - 2024/3

Y1 - 2024/3

N2 - An efficient strategy to obtain a broad array of chiral and achiral heterotropones and their corresponding [4 + 2] cycloadducts is disclosed. This strategy enables access to unique heterotropones and intricate bicyclic structures in high yields and diastereoselectivities through a simple procedure and from easily accessible starting materials.

AB - An efficient strategy to obtain a broad array of chiral and achiral heterotropones and their corresponding [4 + 2] cycloadducts is disclosed. This strategy enables access to unique heterotropones and intricate bicyclic structures in high yields and diastereoselectivities through a simple procedure and from easily accessible starting materials.

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U2 - 10.1021/acs.orglett.3c04080

DO - 10.1021/acs.orglett.3c04080

M3 - Letter

C2 - 38364106

SN - 1523-7060

VL - 26

SP - 1539

EP - 1543

JO - Organic Letters

JF - Organic Letters

IS - 8

ER -

Exploring Heterotropones and Examining Their Propensity to Undergo [4 + 2] Cycloadditions

Abstract

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