Ti(Oi-Pr)4-promoted photoenolization Diels–Alder reaction to construct polycyclic rings and its synthetic applications

Anthracenols with multiple chiral centres are common motifs in natural products. Here, the authors show a highly stereoselective photoenolization/Diels–Alder methodology involving a key Lewis acid reagent enabling the efficient construction of a family of anthracenol derivatives with quaternary cent...

Descripción completa

Guardado en:

Detalles Bibliográficos
Autores principales:	Baochao Yang, Kuaikuai Lin, Yingbo Shi, Shuanhu Gao
Formato:	article
Lenguaje:	EN
Publicado:	Nature Portfolio 2017
Materias:	Science Q
Acceso en línea:	https://doaj.org/article/0af9120aeae34641b0bef29b9a8df013
Etiquetas:	Agregar Etiqueta Sin Etiquetas, Sea el primero en etiquetar este registro!

id	oai:doaj.org-article:0af9120aeae34641b0bef29b9a8df013
record_format	dspace
spelling	oai:doaj.org-article:0af9120aeae34641b0bef29b9a8df0132021-12-02T14:40:58ZTi(Oi-Pr)4-promoted photoenolization Diels–Alder reaction to construct polycyclic rings and its synthetic applications10.1038/s41467-017-00440-82041-1723https://doaj.org/article/0af9120aeae34641b0bef29b9a8df0132017-09-01T00:00:00Zhttps://doi.org/10.1038/s41467-017-00440-8https://doaj.org/toc/2041-1723Anthracenols with multiple chiral centres are common motifs in natural products. Here, the authors show a highly stereoselective photoenolization/Diels–Alder methodology involving a key Lewis acid reagent enabling the efficient construction of a family of anthracenol derivatives with quaternary centers.Baochao YangKuaikuai LinYingbo ShiShuanhu GaoNature PortfolioarticleScienceQENNature Communications, Vol 8, Iss 1, Pp 1-10 (2017)
institution	DOAJ
collection	DOAJ
language	EN
topic	Science Q
spellingShingle	Science Q Baochao Yang Kuaikuai Lin Yingbo Shi Shuanhu Gao Ti(Oi-Pr)4-promoted photoenolization Diels–Alder reaction to construct polycyclic rings and its synthetic applications
description	Anthracenols with multiple chiral centres are common motifs in natural products. Here, the authors show a highly stereoselective photoenolization/Diels–Alder methodology involving a key Lewis acid reagent enabling the efficient construction of a family of anthracenol derivatives with quaternary centers.
format	article
author	Baochao Yang Kuaikuai Lin Yingbo Shi Shuanhu Gao
author_facet	Baochao Yang Kuaikuai Lin Yingbo Shi Shuanhu Gao
author_sort	Baochao Yang
title	Ti(Oi-Pr)4-promoted photoenolization Diels–Alder reaction to construct polycyclic rings and its synthetic applications
title_short	Ti(Oi-Pr)4-promoted photoenolization Diels–Alder reaction to construct polycyclic rings and its synthetic applications
title_full	Ti(Oi-Pr)4-promoted photoenolization Diels–Alder reaction to construct polycyclic rings and its synthetic applications
title_fullStr	Ti(Oi-Pr)4-promoted photoenolization Diels–Alder reaction to construct polycyclic rings and its synthetic applications
title_full_unstemmed	Ti(Oi-Pr)4-promoted photoenolization Diels–Alder reaction to construct polycyclic rings and its synthetic applications
title_sort	ti(oi-pr)4-promoted photoenolization diels–alder reaction to construct polycyclic rings and its synthetic applications
publisher	Nature Portfolio
publishDate	2017
url	https://doaj.org/article/0af9120aeae34641b0bef29b9a8df013
work_keys_str_mv	AT baochaoyang tioipr4promotedphotoenolizationdielsalderreactiontoconstructpolycyclicringsanditssyntheticapplications AT kuaikuailin tioipr4promotedphotoenolizationdielsalderreactiontoconstructpolycyclicringsanditssyntheticapplications AT yingboshi tioipr4promotedphotoenolizationdielsalderreactiontoconstructpolycyclicringsanditssyntheticapplications AT shuanhugao tioipr4promotedphotoenolizationdielsalderreactiontoconstructpolycyclicringsanditssyntheticapplications
_version_	1718390034234605568

Ti(Oi-Pr)4-promoted photoenolization Diels–Alder reaction to construct polycyclic rings and its synthetic applications

Ejemplares similares