Substructure Search

2663

COc1cc(/C=C\c2ccc(Cl)c([N+](=O)[O-])c2)cc(OC)c1OC
Reaction #2993
intended compound
Yield 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
Yield 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
Yield 96.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(/C=C\c2csc(-c3ccccc3)n2)cc(OC)c1OC
Reaction #91486
compounds 3a
Yield 27.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)cc(OC)c1OC.[Br-]
Reaction #157216
3,4,5-trimethoxybenzyltriphenylphosphonium bromide
Yield 96.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(/C=C\c2csc(-c3ccccc3)n2)cc(OC)c1OC
Reaction #157217
compounds 3a
Yield 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
Yield 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
13
Yield 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
17
Yield 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
20
Yield 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
24
Yield 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
46
Yield 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
Yield 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
Yield 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
Yield 49.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)cc(OC)c1OC.[Br-]
Reaction #609745
3,4,5-trimethoxybenzyltriphenylphosphonium bromide
Yield 96.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(/C=C\c2csc(-c3ccccc3)n2)cc(OC)c1OC
Reaction #609746
compounds 3a
Yield 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
Yield 86.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)cc(OC)c1OC.[Br-]
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
Yield 51.0%DOI: 10.6084/m9.figshare.5104873.v1
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