Catalyst-controlled regioselectivity in phosphine catalysis: The synthesis of spirocyclic benzofuranones via regiodivergent [3 + 2] annulations of aurones and an allenoate

10.1039/c7sc02176c

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Bibliographic Details
Main Authors:	Ni, H, Yu, Z, Yao, W, Lan, Y, Ullah, N, Lu, Y
Other Authors:	DEPT OF CHEMISTRY
Format:	Article
Published:	Royal Society of Chemistry 2020
Subjects:	Catalysts Enantioselectivity Hydrogen bonds Peptides Phosphorus compounds Alkyl substitution Annulation products DFT calculation Di-peptides Distortion energy Hydrogen bonding interactions Transition state Regioselectivity
Online Access:	https://scholarbank.nus.edu.sg/handle/10635/174895
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Institution:	National University of Singapore

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spelling	sg-nus-scholar.10635-1748952023-09-13T20:54:30Z Catalyst-controlled regioselectivity in phosphine catalysis: The synthesis of spirocyclic benzofuranones via regiodivergent [3 + 2] annulations of aurones and an allenoate Ni, H Yu, Z Yao, W Lan, Y Ullah, N Lu, Y DEPT OF CHEMISTRY Catalysts Enantioselectivity Hydrogen bonds Peptides Phosphorus compounds Alkyl substitution Annulation products DFT calculation Di-peptides Distortion energy Hydrogen bonding interactions Transition state Regioselectivity 10.1039/c7sc02176c Chemical Science 8 8 5699-5704 2020-09-09T01:19:28Z 2020-09-09T01:19:28Z 2017 Article Ni, H, Yu, Z, Yao, W, Lan, Y, Ullah, N, Lu, Y (2017). Catalyst-controlled regioselectivity in phosphine catalysis: The synthesis of spirocyclic benzofuranones via regiodivergent [3 + 2] annulations of aurones and an allenoate. Chemical Science 8 (8) : 5699-5704. ScholarBank@NUS Repository. https://doi.org/10.1039/c7sc02176c 20416520 https://scholarbank.nus.edu.sg/handle/10635/174895 Royal Society of Chemistry Unpaywall 20200831
institution	National University of Singapore
building	NUS Library
continent	Asia
country	Singapore Singapore
content_provider	NUS Library
collection	ScholarBank@NUS
topic	Catalysts Enantioselectivity Hydrogen bonds Peptides Phosphorus compounds Alkyl substitution Annulation products DFT calculation Di-peptides Distortion energy Hydrogen bonding interactions Transition state Regioselectivity
spellingShingle	Catalysts Enantioselectivity Hydrogen bonds Peptides Phosphorus compounds Alkyl substitution Annulation products DFT calculation Di-peptides Distortion energy Hydrogen bonding interactions Transition state Regioselectivity Ni, H Yu, Z Yao, W Lan, Y Ullah, N Lu, Y Catalyst-controlled regioselectivity in phosphine catalysis: The synthesis of spirocyclic benzofuranones via regiodivergent [3 + 2] annulations of aurones and an allenoate
description	10.1039/c7sc02176c
author2	DEPT OF CHEMISTRY
author_facet	DEPT OF CHEMISTRY Ni, H Yu, Z Yao, W Lan, Y Ullah, N Lu, Y
format	Article
author	Ni, H Yu, Z Yao, W Lan, Y Ullah, N Lu, Y
author_sort	Ni, H
title	Catalyst-controlled regioselectivity in phosphine catalysis: The synthesis of spirocyclic benzofuranones via regiodivergent [3 + 2] annulations of aurones and an allenoate
title_short	Catalyst-controlled regioselectivity in phosphine catalysis: The synthesis of spirocyclic benzofuranones via regiodivergent [3 + 2] annulations of aurones and an allenoate
title_full	Catalyst-controlled regioselectivity in phosphine catalysis: The synthesis of spirocyclic benzofuranones via regiodivergent [3 + 2] annulations of aurones and an allenoate
title_fullStr	Catalyst-controlled regioselectivity in phosphine catalysis: The synthesis of spirocyclic benzofuranones via regiodivergent [3 + 2] annulations of aurones and an allenoate
title_full_unstemmed	Catalyst-controlled regioselectivity in phosphine catalysis: The synthesis of spirocyclic benzofuranones via regiodivergent [3 + 2] annulations of aurones and an allenoate
title_sort	catalyst-controlled regioselectivity in phosphine catalysis: the synthesis of spirocyclic benzofuranones via regiodivergent [3 + 2] annulations of aurones and an allenoate
publisher	Royal Society of Chemistry
publishDate	2020
url	https://scholarbank.nus.edu.sg/handle/10635/174895
_version_	1778169799439810560

Catalyst-controlled regioselectivity in phosphine catalysis: The synthesis of spirocyclic benzofuranones via regiodivergent [3 + 2] annulations of aurones and an allenoate

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