NDLI: Chiral phosphine-catalyzed tunable cycloaddition reactions of allenoates with benzofuranone-derived olefins for a highly regio-, diastereo- and enantioselective synthesis of spiro-benzofuranones† †Electronic supplementary information (ESI) available: Experimental procedures, characterization data of

Content Provider	Semantic Scholar
Author	Wang, De Wang, Guopeng Sun, Yao-Liang Zhu, Shou-Fei Zhou, Q.
Copyright Year	2015
Abstract	The SBIP-catalyzed reaction of benzofuranone alkene (I) with allenes (II) affords γ-addition [3 + 2] cycloadducts (III) with high enantioselectivity, whilst the reaction with allenes (IV) gives rise to α-addition [3 + 2] cycloadducts (V).
Starting Page	7319
Ending Page	7325
Page Count	7
File Format	PDF HTM / HTML
DOI	10.1002/chin.201611120
PubMed reference number	29861963
Volume Number	6
Alternate Webpage(s)	http://www.rsc.org/suppdata/c5/sc/c5sc03135d/c5sc03135d1.pdf
Alternate Webpage(s)	https://pubs.rsc.org/en/content/articlepdf/2015/sc/c5sc03135d
Journal	Chemical Science
Language	English
Access Restriction	Open
Content Type	Text
Resource Type	Article

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