بحث البنية الفرعية

184929

CC1=Nc2ccc(C(=O)O)cc2C1(C)C
Reaction #89789
desired product
المردود 80.1%DOI: 10.6084/m9.figshare.5104873.v1
CC1=Nc2ccc(C(=O)O)cc2C1(C)C
Reaction #89792
desired product
المردود 80.1%DOI: 10.6084/m9.figshare.5104873.v1
CC1=Nc2c(cc(C(=O)O)c3sccc23)C1(C)C
Reaction #717772
2,3,3-trimethyl-3H-thieno[2,3-g]indole-5-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC1=Nc2c(cc(C(=O)O)c3sccc23)C1(C)C
Reaction #717774
2,3,3-trimethyl-3H-thieno[2,3-g]indole-5-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC1=Nc2ccc(C(=O)O)cc2C1(C)C
Reaction #1272134
desired product
المردود 80.1%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(-c2cc[n+]3c(c2)C(C)(C)c2cc(C(=O)[O-])ccc2-3)c2ccccc21
Reaction #2033393
yellow powder
المردود 17.6%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1ccc(-c2cc[n+]3c(c2)C(C)(C)c2cc(C(=O)[O-])ccc2-3)cc1
Reaction #2033395
8-[4-(dimethylamino)phenyl]-10,10-dimethyl-10H-pyrido[1,2-a]indolium-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1