Chloromethyl chloroformate

CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@](O)(C(=O)OCCl)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #1502
3-(Chloromethoxycarbonyl) Cholesterol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(N[C@@H]1CCCN2c3cc(Cl)ccc3Oc3ccccc3[C@H]12)OCCl
Reaction #44437
trans-(7-chloro-2,3,4,14b-tetrahydro-1H-dibenzo[b,f]pyrido[1,2-d][1,4]oxazepin-1-yl)carbamic acid chloromethyl ester
収率 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cl.O=C(c1ccccc1)C1CNCCO1
Reaction #60588
2-benzoylmorpholine hydrochloride
収率 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(OCCl)OCc1cccc(COC(=O)OCCl)n1
Reaction #63261
2,6-bis(chloromethyloxy-carbonyloxymethyl)pyridine
収率 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
O=C(OCCl)OCC1CCCO1
Reaction #174024
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1COC(O)(c2cc(F)cc(F)c2)C(C)N1C(=O)OCCl
Reaction #185225
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCN(CC)C(=O)OCCl
Reaction #191113
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)Nc1ccc(-c2cccs2)cc1NC(=O)c1ccc(CNC(=O)OCCl)cc1
Reaction #198061
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCN1N=C(c2cc(Cl)cc(Cl)c2)N(C(=O)OCCl)CC1=O
Reaction #198265
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)N1CCC(CCOC(=O)OCCl)CC1
Reaction #207639
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(OC(=O)OCCl)C(=O)OCc1ccccc1
Reaction #225003
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C1CCc2ccc(OCCCCN3CCN(c4cccc(Cl)c4Cl)CC3)cc2N1C(=O)OCCl
Reaction #233293
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCOC(=O)OCCl
Reaction #251303
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)C(NC(=O)OCc1ccccc1)C(=O)OCC(C)(C)NC(=O)OCCl
Reaction #253343
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCN(CCCC)C(=O)OCCl
Reaction #265329
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(OCCl)OCCCOCc1ccccc1
Reaction #267810
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCCCCCOC(=O)OCCl
Reaction #280383
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(OCCl)Oc1ccc([N+](=O)[O-])cc1
Reaction #282061
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)CCCC(C)C1CCC2C3CC=C4CC(O)(C(=O)OCCl)CCC4(C)C3CCC12C
Reaction #283308
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)CN(C(=O)OCCl)C(C)C
Reaction #293133
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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