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Reinforcement of double built-in electric fields in spiro-MeOTAD/Ga 2 O 3 /Si p–i–n structure for a high-sensitivity solar-blind UV photovoltaic detec ... - Journal of Materials Chemistry C (RSC Publishing) DOI:10.1039/D1TC03359J
Syntheses and reactivity of spiro-epoxy/aziridine oxindole cores: developments in the past decade - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/D0OB01726D
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![A straightforward, environmentally beneficial synthesis of spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-indoline]-2′,10,12-triones mediated by a nano-ordered reusable catalyst | Scientific Reports](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41598-021-84209-6/MediaObjects/41598_2021_84209_Fig1_HTML.png "A straightforward, environmentally beneficial synthesis of spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-indoline]-2′,10,12-triones mediated by a nano-ordered reusable catalyst | Scientific Reports")
A straightforward, environmentally beneficial synthesis of spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-indoline]-2′,10,12-triones mediated by a nano-ordered reusable catalyst | Scientific Reports
A TADF Emitter Featuring Linearly Arranged Spiro‐Donor and Spiro‐Acceptor Groups: Efficient Nondoped and Doped Deep‐Blue OLEDs with CIEy <0.1 - Xia - 2021 - Angewandte Chemie International Edition - Wiley Online Library
![Positioning of an unprecedented spiro[5.5]undeca ring system into kinase inhibitor space | Scientific Reports](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41598-020-78158-9/MediaObjects/41598_2020_78158_Fig1_HTML.png "Positioning of an unprecedented spiro[5.5]undeca ring system into kinase inhibitor space | Scientific Reports")
Positioning of an unprecedented spiro[5.5]undeca ring system into kinase inhibitor space | Scientific Reports
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Reinforcement of double built-in electric fields in spiro-MeOTAD/Ga 2 O 3 /Si p–i–n structure for a high-sensitivity solar-blind UV photovoltaic detec ... - Journal of Materials Chemistry C (RSC Publishing) DOI:10.1039/D1TC03359J
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![Synthesis of spiro quasi[1]catenanes and quasi[1]rotaxanes via a templated backfolding strategy | Nature Communications](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fncomms15392/MediaObjects/41467_2017_Article_BFncomms15392_Fig1_HTML.jpg "Synthesis of spiro quasi[1]catenanes and quasi[1]rotaxanes via a templated backfolding strategy | Nature Communications")
Synthesis of spiro quasi[1]catenanes and quasi[1]rotaxanes via a templated backfolding strategy | Nature Communications
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![Convenient construction of spiro[indoline-3, 5'-pyrrolo[3, 4-c]carbazole] and spiro[indene-2, 5'-pyrrolo[3, 4-c]carbazole] via acid-catalyzed Diels-Alder reaction](http://www.ccspublishing.org.cn/fileHXH/journal/article/ccl/2021/3/PIC/ccl-32-3-1253-S3.jpg "Convenient construction of spiro[indoline-3, 5'-pyrrolo[3, 4-c]carbazole] and spiro[indene-2, 5'-pyrrolo[3, 4-c]carbazole] via acid-catalyzed Diels-Alder reaction")
Convenient construction of spiro[indoline-3, 5'-pyrrolo[3, 4-c]carbazole] and spiro[indene-2, 5'-pyrrolo[3, 4-c]carbazole] via acid-catalyzed Diels-Alder reaction
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Syntheses and reactivity of spiro-epoxy/aziridine oxindole cores: developments in the past decade - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/D0OB01726D
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Syntheses and reactivity of spiro-epoxy/aziridine oxindole cores: developments in the past decade - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/D0OB01726D
