Mercury(II) acetate

OC1CCCCC2(C1)OCCO2
Reaction #1000
3-hydroxycycloheptanone ethylene ketal
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1nnc(N2N=C(c3ccc([N+](=O)[O-])cc3)c3cc4c(cc3C[C@H]2C)OCO4)o1
Reaction #53357
title compound
Выход 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Cc1cnc(-c2ccc3c(c2)CCN(C(=O)OC(C)(C)C)CC3)o1
Reaction #61496
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
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.v1uspto-grants-2013_09
OC1CCCC1Oc1ccc(Oc2ccccc2)cc1
Reaction #75058
2-(4-phenoxyphenoxy)cyclopentan-1-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
CCC1(C)Cc2ccccc2C1
Reaction #348711
2-ethyl-2-methyl-indan
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_08
CCCC(S)C(=O)N[C@@H](CCc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)O
Reaction #363296
title compound
Выход 58.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CCCC(S)C(=O)N[C@@H](CCc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)NC
Reaction #363299
title compound
Выход 80.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
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.v1uspto-grants-2014_11
COC(=O)C(C)OC(C)(C)C(C)=O
Reaction #428831
2-(1,1-dimethyl-2-oxopropoxy)propionic acid methyl ester
Выход 141.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CCC1(C)CC(=O)C(C)(CC)O1
Reaction #428851
2,5-diethyl-2,5-di-methyldihydrofuran-3-one
Выход 435.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
c1cc(NC2=NCCO2)c2occc2c1
Reaction #521737
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1983_08
Cc1c(Br)cccc1CCO
Reaction #533580
subtitled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
COC(=O)COC(C)(C)C(C)=O
Reaction #565475
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_11
COC(=O)COC(C)C(C)=O
Reaction #565485
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_11
CC#CCn1c(N2CCN(C(=O)OC(C)(C)C)CC2)nc(CO)c1C(=O)OCC
Reaction #588576
title compound
Выход 25.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
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.v1uspto-grants-2015_08
CCOC(=O)N(CCC(=O)CO)Cc1ccccc1
Reaction #613917
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
OC1CCCCC2(C1)OCCO2
Reaction #670015
3-Hydroxycycloheptanone ethylene ketal
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_07
Clc1cccc(-n2nnnc2NCC2CCCCC2)c1Cl
Reaction #732836
title compound
Выход 56.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
Страница 1Далее