子结构搜索

ClCI

FC(F)(F)c1ccccc1C1CO1
Reaction #2158
oil
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NC[C@@H]1C[C@@H]1c1ccncc1
Reaction #11572
titled compound
收率 3.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OP(=O)(OCCl)OC(C)(C)C
Reaction #48488
di-tert-butyl chloromethyl phosphate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OP(=O)(OCCl)OC(C)(C)C
Reaction #48489
di-tert-butyl chloromethyl phosphate
收率 343.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OP(=O)(OCCl)OC(C)(C)C
Reaction #48490
di-tert-butyl chloromethyl phosphate
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](c1ccccc1)[N+]12CC[C@H](CC(=O)C1)C2.[Cl-]
Reaction #50927
(5R)-3-oxo-1-[(1S)-1-phenylethyl]-1-azoniabicyclo[3.2.1]octane chloride
收率 36.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1cc(F)cc(F)c1)C(=O)CCl
Reaction #51490
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1cc(F)cc(F)c1)C(=O)CCl
Reaction #51500
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](c1ccccc1)[N+]12CC[C@H](CC(=O)C1)C2.[Cl-]
Reaction #51650
(5R)-3-oxo-1-[(1S)-1-phenylethyl]-1-azoniabicyclo[3.2.1]octane chloride
收率 36.6%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](c1ccccc1)[N+]12CC[C@H](CC(=O)C1)C2.[Cl-]
Reaction #53433
(5R)-3-oxo-1-[(1S)-1-phenylethyl]-1-azoniabicyclo[3.2.1]octane chloride
收率 36.6%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OB(CCl)OC1(C)C
Reaction #67882
compound
收率 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC1(c2ccc([C@H](C)N[S@](=O)C(C)(C)C)c(F)c2)CC1
Reaction #85698
(R)—N—((S)-1-(4-(1-ethoxycyclopropyl)-2-fluorophenyl)ethyl)-2-methylpropane-2-sulfinamide
收率 28.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(COC2CC2)CC1
Reaction #156307
tert-butyl 4-[(cyclopropyloxy)methyl]piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)Cc1ccccc1OC1CC1
Reaction #169393
title compound
收率 53.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(OC2CC2)c1
Reaction #173004
DOI: 10.1039/C8SC04228D
CC(C)C(NC(=O)OCc1ccccc1)C(=O)OCCOc1ccc(C(=O)O)cc1
Reaction #177213
DOI: 10.1039/C8SC04228D
O=C1N(C(c2ccccc2)c2ccccc2)c2ccccc2C12COc1cc(OCc3ccccc3)ccc12
Reaction #184054
DOI: 10.1039/C8SC04228D
FC(F)(Cl)C(F)(Cl)C(F)(F)C(F)(F)I
Reaction #196440
DOI: 10.1039/C8SC04228D
O=C(OCc1ccccc1)N1CCC2CC21
Reaction #220003
desired product
收率 50.0%DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc(OC2CC2)cc1
Reaction #222954
DOI: 10.1039/C8SC04228D
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