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683578

CCOC(=O)c1cc(CC)cnc1C(=O)OCC
Reaction #4014
title product
収率 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(CC)cnc1C
Reaction #4015
title product
収率 43.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2ncnn2c(O)c1Cl
Reaction #11292
5-Chloro-4-hydroxy-6-methyl-1,3,3a,7-tetraazaindene
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Cc1ncc(CO)s1
Reaction #42332
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Cl)=NNc1ccc(Cl)cc1
Reaction #48033
ethyl 2-chloro[(4-chlorophenyl)hydrazono]acetate
収率 73.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Cl)C(=O)CC
Reaction #55098
ethyl 2-chloro-3-oxopentanoate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Cl)C(=O)CC
Reaction #55767
ethyl 2-chloro-3-oxopentanoate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1oc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)nc1C
Reaction #71897
title compound
収率 31.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Cl)C(=O)c1ccccc1
Reaction #75953
product
収率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(N)nc1-c1ccccc1
Reaction #75954
ethyl 2-amino-4-phenyl-1,3-thiazole-5-carboxylate
収率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Cl)C=O
Reaction #80966
Ethyl 2-Chloro-2-formylacetate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cncs1
Reaction #81103
desired compound
収率 33.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Cl)C=O
Reaction #82202
Ethyl 2-Chloro-2-formylacetate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cncs1
Reaction #82203
desired compound
収率 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(-c2ccc(C)cc2)nc1C
Reaction #86826
ethyl 4-methyl-2-p-tolylthiazole-5-carboxylate
収率 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(C)nc2c(OCC3CCCCC3)cc(C)cn12
Reaction #92678
ethyl 8-(cyclohexylmethoxy)-2,6-dimethylimidazo[1,2-a]pyridine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(C(Cl)(Cl)Cl)nc(O)c1Cl
Reaction #94998
5-Chloro-4-Hydroxy-6-Methyl-2-Trichloromethylpyrimidine
収率 31.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1oc(N)nc1C
Reaction #157410
ethyl 2-amino-4-methyloxazole-5-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(Cl)CCCNC1=O
Reaction #158353
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(Oc2cc(F)c(F)c(F)c2)CCCNC1=O
Reaction #158354
title compound
収率 79.8%DOI: 10.6084/m9.figshare.5104873.v1
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