Home > Research > Publications & Outputs > A light touch for complex products

Research

Associated organisational unit

Electronic data

Links

Text available via DOI:

View graph of relations

A light touch for complex products

Research output: Contribution to Journal/Magazine › Journal article

Published

Standard

A light touch for complex products. / Coote, S.
In: Nature Chemistry, Vol. 12, 01.10.2020, p. 889-890.

Research output: Contribution to Journal/Magazine › Journal article

Harvard

Coote, S 2020, 'A light touch for complex products', Nature Chemistry, vol. 12, pp. 889-890. https://doi.org/10.1038/s41557-020-0536-y

APA

Coote, S. (2020). A light touch for complex products. Nature Chemistry, 12, 889-890. https://doi.org/10.1038/s41557-020-0536-y

Vancouver

Coote S. A light touch for complex products. Nature Chemistry. 2020 Oct 1;12:889-890. Epub 2020 Sept 23. doi: 10.1038/s41557-020-0536-y

Author

Coote, S. / A light touch for complex products. In: Nature Chemistry. 2020 ; Vol. 12. pp. 889-890.

Bibtex

@article{328aaba24ce3491da39063430f30468d,
title = "A light touch for complex products",
abstract = "The [2+2] photocycloaddition of two double-bond moieties is arguably the most efficient way to form a four-membered ring, but this route is rarely used to construct azetidine rings. Now, the development of an isoxazoline carboxylate cycloaddition partner offers a general approach to synthesize diverse azetidine products.",
author = "S. Coote",
year = "2020",
month = oct,
day = "1",
doi = "10.1038/s41557-020-0536-y",
language = "English",
volume = "12",
pages = "889--890",
journal = "Nature Chemistry",
issn = "1755-4330",
publisher = "Nature Publishing Group",

}

RIS

TY - JOUR

T1 - A light touch for complex products

AU - Coote, S.

PY - 2020/10/1

Y1 - 2020/10/1

N2 - The [2+2] photocycloaddition of two double-bond moieties is arguably the most efficient way to form a four-membered ring, but this route is rarely used to construct azetidine rings. Now, the development of an isoxazoline carboxylate cycloaddition partner offers a general approach to synthesize diverse azetidine products.

AB - The [2+2] photocycloaddition of two double-bond moieties is arguably the most efficient way to form a four-membered ring, but this route is rarely used to construct azetidine rings. Now, the development of an isoxazoline carboxylate cycloaddition partner offers a general approach to synthesize diverse azetidine products.

U2 - 10.1038/s41557-020-0536-y

DO - 10.1038/s41557-020-0536-y

M3 - Journal article

VL - 12

SP - 889

EP - 890

JO - Nature Chemistry

JF - Nature Chemistry

SN - 1755-4330

ER -