بحث البنية الفرعية

4070

OC1CCCCC2(C1)OCCO2
Reaction #1000
3-hydroxycycloheptanone ethylene ketal
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nnc(N2N=C(c3ccc([N+](=O)[O-])cc3)c3cc4c(cc3C[C@H]2C)OCO4)o1
Reaction #53357
title compound
المردود 51.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cnc(-c2ccc3c(c2)CCN(C(=O)OC(C)(C)C)CC3)o1
Reaction #61496
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc(C2CC2)[c]([Pb+3])c1.CC(=O)[O-].CC(=O)[O-].CC(=O)[O-]
Reaction #68756
5-bromo-2-cyclopropylphenyl lead triacetate
DOI: 10.6084/m9.figshare.5104873.v1
OC1CCCC1Oc1ccc(Oc2ccccc2)cc1
Reaction #75058
2-(4-phenoxyphenoxy)cyclopentan-1-ol
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(C(C)N(c2nc3ccccc3n2C)[C@H]2CC[C@H](C(C)(C)C)CC2)cc1
Reaction #317202
ethyl 4-{1-[(trans-4-tert-butylcyclohexyl)(1-methyl-1H-benzimidazol-2-yl)amino]ethyl}benzoate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc2c(c1)CCC2N(c1nc2ccccc2n1C)[C@H]1CC[C@H](C(C)(C)C)CC1
Reaction #317205
methyl 1-[(trans-4-tert-butylcyclohexyl)(1-methyl-1H-benzimidazol-2-yl)amino]indane-5-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cc2c[nH]c(=NC(=O)OCC3c4ccccc4-c4ccccc43)n2cc1C(=O)NC
Reaction #336911
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CCC1(C)Cc2ccccc2C1
Reaction #348711
2-ethyl-2-methyl-indan
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(S)C(=O)N[C@@H](CCc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)O
Reaction #363296
title compound
المردود 58.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(S)C(=O)N[C@@H](CCc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)NC
Reaction #363299
title compound
المردود 80.5%DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc(C2CC2)[c]([Pb+3])c1.CC(=O)[O-].CC(=O)[O-].CC(=O)[O-]
Reaction #426657
5-bromo-2-cyclopropylphenyl lead triacetate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)OC(C)(C)C(C)=O
Reaction #428831
2-(1,1-dimethyl-2-oxopropoxy)propionic acid methyl ester
المردود 141.7%DOI: 10.6084/m9.figshare.5104873.v1
CCC1(C)CC(=O)C(C)(CC)O1
Reaction #428851
2,5-diethyl-2,5-di-methyldihydrofuran-3-one
المردود 435.1%DOI: 10.6084/m9.figshare.5104873.v1
c1cc(NC2=NCCO2)c2occc2c1
Reaction #521737
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Br)cccc1CCO
Reaction #533580
subtitled compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)COC(C)(C)C(C)=O
Reaction #565475
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)COC(C)C(C)=O
Reaction #565485
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC#CCn1c(N2CCN(C(=O)OC(C)(C)C)CC2)nc(CO)c1C(=O)OCC
Reaction #588576
title compound
المردود 25.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)[O-].CC(=O)[O-].CC(=O)[O-].Cc1cc(OCc2ccccc2)cc(C)[c]1[Pb+3]
Reaction #599764
4-benzyloxy-2,6-dimethylphenyl lead triacetate
DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي