参与 466 个反应

2013

CC(C)(C)OC(=O)NC1(C(F)(F)F)CCN(Cc2ccccc2)C1
Reaction #1983
title compound
收率 96.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)[O-].C[N+](C)(C)C
Reaction #7362
tetramethylammonium methyl-carbonate
收率 80.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cn1c(C(=O)/C=N/N)cc2cccc(Br)c21
Reaction #40900
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1c(-c2ccccc2)c(F)c2oc(C(=O)N(C)C)nc2c1C#N
Reaction #45650
compound
收率 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
N#Cc1nccc(Oc2ccc(N)c3ccccc23)n1
Reaction #51810
4-(4-amino-naphthalen-1-yloxy)-pyrimidine-2-carbonitrile
收率 54.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Cc1ccc(COC(=O)C(C)c2ccc(CC(C)C)cc2)cc1
Reaction #54735
2-(4-isobutylphenyl)propionic acid-p-methylbenzyl ester
收率 84.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
C=C1CCc2c(c3ccccc3n2C)C1=O
Reaction #65051
9-methyl-3-methylene-1,2,3,9-tetrahydro-4H-carbazol-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCc1csc([C@H](Cc2ccc(NS(=O)(=O)[O-])cc2)NC(=O)[C@H](Cc2ccccc2)NC(=O)OC)n1.[Na+]
Reaction #88342
desired compound
收率 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCCCCC(=O)OC(C)C(=O)O[C@H]1[C@@H](CC)C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@@]21C
Reaction #93010
above-identified compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
C=C1C[C@@H]2[C@H](CC[C@]3(C)C(C(C)=O)=C(CS(=O)c4ccccc4)C[C@@H]23)[C@@]2(C)CCC(=O)C=C12
Reaction #93685
6-Methylene-16-(phenylsulfinylmethyl)pregna-4,16-diene-3,20-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
Cc1ccc(COC(=O)C(C)c2ccc(CC(C)C)cc2)cc1
Reaction #176322
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CCC1(C)CC(c2cncc(Cl)c2)C(c2ccc(Cl)cc2)N(C(CC)CO)C1=O
Reaction #180857
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CS(=O)(=O)On1nnc2ccccc21
Reaction #181299
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(COCCCCCCCCCCCCC1CCCCC1)CS(=O)(=O)CCC[N+](C)(C)C
Reaction #181460
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(S(=O)(=O)OCCCCc2c(F)c(F)c(F)c(F)c2F)cc1
Reaction #182273
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C[N+](C)(C)CC(O)CO
Reaction #183876
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCC(CC)O[SH]1C=C(Oc2cc(F)ccc2F)NN(N)N1
Reaction #184173
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC(OC(=O)c1ccc(NCCCCCCCCCCCCCCCC(F)(F)F)cc1)C(=O)OC
Reaction #185095
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=c1c(Cl)nsnc1Sc1ccccc1
Reaction #185601
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#CC1(c2ccccc2)CCCC(=O)C1
Reaction #189351
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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