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2663

$COc1cc(/C=C\c2ccc(Cl)c([N+](=O)[O-])c2)cc(OC)c1OC$

Reaction #2993

intended compound

Ausbeute 50.9%DOI: 10.6084/m9.figshare.5104873.v1

$COc1cc(/C=C\c2ccc(C)c([N+](=O)[O-])c2)cc(OC)c1OC$

Reaction #2994

intended compound

Ausbeute 49.6%DOI: 10.6084/m9.figshare.5104873.v1

COc1cc(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)cc(OC)c1OC.[Br-]

Reaction #91485

3,4,5-trimethoxybenzyltriphenylphosphonium bromide

Ausbeute 96.4%DOI: 10.6084/m9.figshare.5104873.v1

$COc1cc(/C=C\c2csc(-c3ccccc3)n2)cc(OC)c1OC$

Reaction #91486

compounds 3a

Ausbeute 27.8%DOI: 10.6084/m9.figshare.5104873.v1

Reaction #157216

3,4,5-trimethoxybenzyltriphenylphosphonium bromide

Ausbeute 96.4%DOI: 10.6084/m9.figshare.5104873.v1

$COc1cc(/C=C\c2csc(-c3ccccc3)n2)cc(OC)c1OC$

Reaction #157217

compounds 3a

Ausbeute 27.8%DOI: 10.6084/m9.figshare.5104873.v1

$COc1cc(/C=C\c2ccc(OC)c([N+](=O)[O-])c2[N+](=O)[O-])cc(OC)c1OC$

Reaction #218275

2′,3′-Dinitro-3,4,4′,5-tetramethoxy-(Z)-stilbene

Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1

$CCc1ccc(/C=C\c2cc(OC)c(OC)c(OC)c2)c(O[Si](C)(C)C(C)(C)C)c1O[Si](C)(C)C(C)(C)C$

Reaction #305428

Ausbeute 21.5%DOI: 10.6084/m9.figshare.5104873.v1

$COc1cc(/C=C\c2ccc(C)c(O[Si](C)(C)C(C)(C)C)c2O[Si](C)(C)C(C)(C)C)cc(OC)c1OC$

Reaction #305432

Ausbeute 48.7%DOI: 10.6084/m9.figshare.5104873.v1

$COc1cc(/C=C\c2cc(Br)cc(O[Si](C)(C)C(C)(C)C)c2O[Si](C)(C)C(C)(C)C)cc(OC)c1OC$

Reaction #305433

Ausbeute 55.9%DOI: 10.6084/m9.figshare.5104873.v1

$COc1cc(/C=C\c2cc(-c3ccccc3)cc(O[Si](C)(C)C(C)(C)C)c2O[Si](C)(C)C(C)(C)C)cc(OC)c1OC$

Reaction #305437

Ausbeute 27.5%DOI: 10.6084/m9.figshare.5104873.v1

$COc1cc(/C=C\c2ccc([N+](=O)[O-])c(O)c2O[Si](C)(C)C(C)(C)C)cc(OC)c1OC$

Reaction #305454

Ausbeute 36.6%DOI: 10.6084/m9.figshare.5104873.v1

$COc1ccc(/C=C\c2cc(OC)c(OC)c(OC)c2)cc1[N+](=O)[O-]$

Reaction #347273

intended compound

Ausbeute 43.3%DOI: 10.6084/m9.figshare.5104873.v1

$COc1cc(/C=C\c2ccc(Cl)c([N+](=O)[O-])c2)cc(OC)c1OC$

Reaction #347275

intended compound

Ausbeute 50.9%DOI: 10.6084/m9.figshare.5104873.v1

$COc1cc(/C=C\c2ccc(C)c([N+](=O)[O-])c2)cc(OC)c1OC$

Reaction #347276

intended compound

Ausbeute 49.6%DOI: 10.6084/m9.figshare.5104873.v1

Reaction #609745

3,4,5-trimethoxybenzyltriphenylphosphonium bromide

Ausbeute 96.4%DOI: 10.6084/m9.figshare.5104873.v1

$COc1cc(/C=C\c2csc(-c3ccccc3)n2)cc(OC)c1OC$

Reaction #609746

compounds 3a

Ausbeute 27.8%DOI: 10.6084/m9.figshare.5104873.v1

COc1cc(C[PH](c2ccccc2)(c2ccccc2)c2ccccc2)cc(OC)c1OC.[Br-]

Reaction #686978

3,4,5-trimethoxyl benzyl triphenylphosphine bromide

Ausbeute 86.4%DOI: 10.6084/m9.figshare.5104873.v1

Reaction #953228

3,4,5-trimethoxy-benzyltriphenylphosphonium bromide

DOI: 10.6084/m9.figshare.5104873.v1

$COc1cc(/C=C\c2ccc(OC)c([N+](=O)[O-])c2[N+](=O)[O-])cc(OC)c1OC$

Reaction #983576

2′,3′-Dinitro-3,4,4′,5-tetramethoxy-(Z)-stilbene

Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1

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