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1397988

COc1ccc2c(c1I)OC(C(F)(F)F)C(C(=O)O)=C2
Reaction #260401
DOI: 10.1039/C8SC04228D
CCOC(=O)C1=Cc2ccc(OC)c(I)c2OC1C(F)(F)F
Reaction #297237
DOI: 10.1039/C8SC04228D
COc1cc2c(cc1I)C=C(C(=O)O)C(C(F)(F)F)O2
Reaction #406172
DOI: 10.1039/C8SC04228D
C=Cc1cc2c(cc1OC)OC(C(F)(F)F)C(C(=O)OCC)=C2
Reaction #910686
DOI: 10.1039/C8SC04228D
CCOC(=O)C1=Cc2cc(I)c(OC)cc2OC1C(F)(F)F
Reaction #942195
light yellow solid
Rendimiento 86.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1I)C=C(C(=O)O)C(C(F)(F)F)O2
Reaction #942196
light yellow solid
Rendimiento 89.3%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1cc2c(cc1OC)OC(C(F)(F)F)C(C(=O)OCC)=C2
Reaction #942197
ethyl 7-methoxy-2-(trifluoromethyl)-6-vinyl-2H-chromene-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=Cc2ccc(OC)c(I)c2OC1C(F)(F)F
Reaction #942205
light yellow solid
Rendimiento 14.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1I)OC(C(F)(F)F)C(C(=O)O)=C2
Reaction #942206
light yellow solid
Rendimiento 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@H](N)Cc1ccc(O)cc1.O=C(O)C=Cc1ccc(O)c(I)c1
Reaction #1539620
3-(3-iodo-4-hydroxyphenyl)-2-propenoic acid tyrosine ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C=Cc1cc(I)c(O)c(I)c1
Reaction #1927097
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=Cc2cc(I)c(OC)cc2OC1C(F)(F)F
Reaction #2233331
DOI: 10.1039/C8SC04228D