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  • ChemInform Abstract: Synthesis of 9-Aryl-9,10-dihydrophenanthrenes by Domino [3 + 3] Annulation/Ring-Opening/Friedel—Crafts Alkylation Reactions of 1,3-Bis(trimethylsilyloxy)-1,3-butadienes
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ChemInform 2011, 42, issue 06 © 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Phenanthrene derivatives Q 1090 DOI: 10.1002/chin.201106115 Synthesis of 9-Aryl-9,10-dihydrophenanthrenes by Domino [3 + 3] Annula- tion/Ring-Opening/Friedel—Crafts Alkylation Reactions of 1,3-Bis(trimethyl- silyloxy)-1,3-butadienes with 3-Aroyl-5-aryl-4,5-dihydrofurans. — (LAU, M.; SHER, M.; VILLINGER, A.; FISCHER, C.; LANGER*, P.; Eur. J. Org. Chem. 2010, 26, 5118-5127, http://dx.doi.org/10.1002/ejoc.201000451 ; Inst. Chem., Univ. Rostock, D-18059 Rostock, Germany; Eng.) — Klein 06- 115

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Page 1: ChemInform Abstract: Synthesis of 9-Aryl-9,10-dihydrophenanthrenes by Domino [3 + 3] Annulation/Ring-Opening/Friedel—Crafts Alkylation Reactions of 1,3-Bis(trimethylsilyloxy)-1,3-butadienes

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Phenanthrene derivativesQ 1090 DOI: 10.1002/chin.201106115

Synthesis of 9-Aryl-9,10-dihydrophenanthrenes by Domino [3 + 3] Annula-tion/Ring-Opening/Friedel—Crafts Alkylation Reactions of 1,3-Bis(trimethyl-silyloxy)-1,3-butadienes with 3-Aroyl-5-aryl-4,5-dihydrofurans. — (LAU, M.; SHER, M.; VILLINGER, A.; FISCHER, C.; LANGER*, P.; Eur. J. Org. Chem. 2010, 26, 5118-5127, http://dx.doi.org/10.1002/ejoc.201000451 ; Inst. Chem., Univ. Rostock, D-18059 Rostock, Germany; Eng.) — Klein

06- 115

ChemInform 2011, 42, issue 06 © 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim

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1,3-Butadiene Reference Exposure Levels - OEHHA · PDF fileSRP DRAFT September 2012 Appendix D1 1 Butadiene 1,3-Butadiene Reference Exposure Levels (butadiene; buta-1,3-diene; biethylene;

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Reversible Two-Electron Redox Reactions Involving Tetralithio ...hpc.pku.edu.cn/docs/pdf/a20191230163.pdf1,3-butadienes with low-valent transition metal complexes generated a number

Dimerization of isoquinolinium ylide and 1,3-dipolar ...scientiairanica.sharif.edu/article_3430_bcc8fdc6b5631d4a955d1f6896... · Dimerization and 1,3-dipolar cycloaddition reactions

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