Leader
|
|
|
00000nz a2200037n 45 0 |
001
|
|
|
WKP|Q51199060
(VIAF cluster)
(Authority/Source Record)
|
003
|
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|
WKP |
005
|
|
|
20241121000327.0 |
008
|
|
|
241121nneanz||abbn n and d |
035
|
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|
‡a
(WKP)Q51199060
|
024
|
|
|
‡a
0000-0002-0090-2894
‡2
orcid
|
035
|
|
|
‡a
(OCoLC)Q51199060
|
100
|
0 |
|
‡a
Yang Li
‡c
researcher ORCID: 0000-0002-0090-2894
‡9
en
|
670
|
|
|
‡a
Author's Arene Trifunctionalization with Highly Fused Ring Systems through a Domino Aryne Nucleophilic and Diels-Alder Cascade
|
670
|
|
|
‡a
Author's Aryne 1,2,3-Trifunctionalization with Aryl Allyl Sulfoxides
|
670
|
|
|
‡a
Author's Aryne multifunctionalization with benzdiyne and benztriyne equivalents
|
670
|
|
|
‡a
Author's Aryne Trifunctionalization Enabled by 3-Silylaryne as a 1,2-Benzdiyne Equivalent
|
670
|
|
|
‡a
Author's Cyclohexenynone Precursors: Preparation via Oxidative Dearomatization Strategy and Reactivity
|
670
|
|
|
‡a
Author's Diamination of Domino Aryne Precursor with Sulfonamides
|
670
|
|
|
‡a
Author's Domino Aryne Annulation via a Nucleophilic-Ene Process.
|
670
|
|
|
‡a
Author's Domino aryne precursor: efficient construction of 2,4-disubstituted benzothiazoles.
|
670
|
|
|
‡a
Author's Selective Aryne Formation via Grob Fragmentation from the [2+2] Cycloadducts of 3-Triflyloxyarynes.
|
670
|
|
|
‡a
Author's Strategies toward Aryne Multifunctionalization via 1,2-Benzdiyne and Benzyne
|
909
|
|
|
‡a
(orcid) 0000000200902894
‡9
1
|
919
|
|
|
‡a
diaminationofdominoaryneprecursorwithsulfonamides
‡A
Diamination of Domino Aryne Precursor with Sulfonamides
‡9
1
|
919
|
|
|
‡a
dominoaryneannulationviaanucleophiliceneprocess
‡A
Domino Aryne Annulation via a Nucleophilic-Ene Process.
‡9
1
|
919
|
|
|
‡a
dominoaryneprecursorefficientconstructionof24disubstitutedbenzothiazoles
‡A
Domino aryne precursor: efficient construction of 2,4-disubstituted benzothiazoles.
‡9
1
|
919
|
|
|
‡a
selectivearyneformationviagrobfragmentationfromthecycloadductsof3triflyloxyarynes
‡A
Selective Aryne Formation via Grob Fragmentation from the [2+2] Cycloadducts of 3-Triflyloxyarynes.
‡9
1
|
919
|
|
|
‡a
strategiestowardarynemultifunctionalizationvia12benzdiyneandbenzyne
‡A
Strategies toward Aryne Multifunctionalization via 1,2-Benzdiyne and Benzyne
‡9
1
|
919
|
|
|
‡a
arenetrifunctionalizationwithhighlyfusedringsystemsthroughadominoarynenucleophilicanddielsaldercascade
‡A
Arene Trifunctionalization with Highly Fused Ring Systems through a Domino Aryne Nucleophilic and Diels-Alder Cascade
‡9
1
|
919
|
|
|
‡a
aryne123trifunctionalizationwitharylallylsulfoxides
‡A
Aryne 1,2,3-Trifunctionalization with Aryl Allyl Sulfoxides
‡9
1
|
919
|
|
|
‡a
arynemultifunctionalizationwithbenzdiyneandbenztriyneequivalents
‡A
Aryne multifunctionalization with benzdiyne and benztriyne equivalents
‡9
1
|
919
|
|
|
‡a
arynetrifunctionalizationenabledby3silylaryneasa12benzdiyneequivalent
‡A
Aryne Trifunctionalization Enabled by 3-Silylaryne as a 1,2-Benzdiyne Equivalent
‡9
1
|
919
|
|
|
‡a
cyclohexenynoneprecursorspreparationviaoxidativedearomatizationstrategyandreactivity
‡A
Cyclohexenynone Precursors: Preparation via Oxidative Dearomatization Strategy and Reactivity
‡9
1
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|
|
|
‡2
CYT|AC000632189
|
996
|
|
|
‡2
BNF|17772739
|
996
|
|
|
‡2
DNB|1029457344
|
996
|
|
|
‡2
DNB|120940892
|
996
|
|
|
‡2
DNB|1251908349
|
996
|
|
|
‡2
SUDOC|143772899
|
996
|
|
|
‡2
ISNI|000000001651607X
|
996
|
|
|
‡2
ISNI|0000000054300499
|
996
|
|
|
‡2
CAOONL|ncf11520012
|
996
|
|
|
‡2
LC|n 2016010079
|
996
|
|
|
‡2
DNB|1322738920
|
996
|
|
|
‡2
DNB|141573511
|
996
|
|
|
‡2
LC|n 2012028119
|
996
|
|
|
‡2
DNB|1250756790
|
996
|
|
|
‡2
CYT|AC000523020
|
996
|
|
|
‡2
ISNI|0000000117978791
|
997
|
|
|
‡a
0 0 lived 0 0
‡9
1
|