بحث البنية الفرعية

6016

C[C@@H]1COS(=O)(=O)N1c1ccccn1
Reaction #990
(R)-4-methyl-3-(2-pyridyl)-[1,2,3]oxathiazolidine-2,2-dioxide
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1C[C@@H](C(=O)O)N(C(=O)OC(C)(C)C)C1=O
Reaction #2977
product
المردود 54.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCC1CCCCCCCCCCC1
Reaction #65585
white solid
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC1CCC(C=O)CC1
Reaction #76382
4-pentyl-cyclohexanecarboxaldehyde
المردود 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)S(=O)(=O)NCc1ccc(Cl)c(-c2nn(-c3ccc(C(F)(F)F)cc3)c(=O)[nH]2)c1
Reaction #87842
desired product
المردود 25.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc(C(=O)O)c([N+](=O)[O-])c1
Reaction #155634
4-tert-Butyl-2-nitro-benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Cl)nc2c1C(=O)N(C(=O)OC(C)(C)C)CC2
Reaction #168007
tert-butyl 2-chloro-4-methyl-5-oxo-7,8-dihydro-1,6-naphthyridine-6(5H)-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CNC(=O)C(=O)NCC(C)=O
Reaction #175665
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(Oc2ccc(S(=O)(=O)C(F)(F)F)cc2)CC1
Reaction #178212
DOI: 10.1039/C8SC04228D
COCCCOS(=O)(=O)OCCCOC
Reaction #179084
DOI: 10.1039/C8SC04228D
CN(CCC1CCC(CC(=O)O)CC1)C(=O)OC(C)(C)C
Reaction #186636
DOI: 10.1039/C8SC04228D
O=C1C(O)OCN1c1ccc(Cl)c(Br)c1
Reaction #188519
DOI: 10.1039/C8SC04228D
CN(CCC1CCC(C(=O)O)CC1)C(=O)OC(C)(C)C
Reaction #192434
DOI: 10.1039/C8SC04228D
O=C(O)c1c(F)cc(F)c(F)c1F
Reaction #195290
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)CCCCON=[N+]([O-])N1CCCC1C(=O)O
Reaction #196593
DOI: 10.1039/C8SC04228D
CC(=O)OC1CCC2(C)C(CCC3C2CC(OC(C)=O)C2(C)C(C(C)=O)CCC32)C1
Reaction #200002
DOI: 10.1039/C8SC04228D
O=Cc1nc2c(N3CCOCC3)nc(Cl)nc2s1
Reaction #207161
DOI: 10.1039/C8SC04228D
CC(O[Si](C)(C)C(C)(C)C)C1C(=O)NC1CC(=O)c1cccc(CC(=O)O)c1
Reaction #213558
DOI: 10.1039/C8SC04228D
O=C(O)CCCC1CCCCCCCCCCC1
Reaction #216716
white solid
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(-n2nc(C(F)(F)F)cc2C(=O)O)ccc1F
Reaction #224977
DOI: 10.1039/C8SC04228D
الصفحة 1التالي