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367086

CN1CCC=C(CO)C1
Reaction #40778
colorless oil
収率 98.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CC(c3cccc(F)c3F)=CC[C@@H](NC(=O)OCc3ccccc3)C2=O)c(OC)c1
Reaction #42664
title compound
収率 57.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CC=C(c2cccc(F)c2F)CNC1=O)OCc1ccccc1
Reaction #42665
title compound
収率 66.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2csc3c(/C=C/CCN4CCC(N)CC4)cnc(N)c23)ccc1NC(=O)c1cc2ccccc2n1C
Reaction #45493
title compound
収率 33.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2csc3c(/C=C/CCN4CCC(CN)CC4)cnc(N)c23)ccc1NC(=O)c1cc2ccccc2n1C
Reaction #45494
title compound
収率 30.0%DOI: 10.6084/m9.figshare.5104873.v1
C[NH+]1CCC=C(C(=O)O)C1.[Cl-]
Reaction #47744
product
収率 46.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2CC(c3cccc(F)c3F)=CC[C@@H](NC(=O)OCc3ccccc3)C2=O)c(OC)c1
Reaction #48408
title compound
収率 57.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CC=C(c2cccc(F)c2F)CNC1=O)OCc1ccccc1
Reaction #48409
title compound
収率 66.4%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@]1(O)C[C@H]2CN(CCc3c([nH]c4c(I)cccc34)[C@@](C(=O)OC)(c3cc4c(cc3OC)N(C)[C@H]3[C@@](O)(C(=O)OC)[C@H](OC(C)=O)[C@]5(CC)C=CCN6CC[C@]43[C@@H]65)C2)C1
Reaction #48763
12′-iodovinblastine
収率 112.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C=CC2=CN(S(=O)(=O)c3ccccc3)C=C3CC(NC4CC4)C(=C23)C1
Reaction #53621
titled compound
収率 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[N-]C(C)C.[Li+]
Reaction #53622
LDA
DOI: 10.6084/m9.figshare.5104873.v1
CCC1=C2CC(N(C)C)C3=C2C(=CN1S(=O)(=O)c1ccccc1)C=COC3
Reaction #53623
titled compound
収率 98.4%DOI: 10.6084/m9.figshare.5104873.v1
CCC1=C2CC(N(C)C)C3=C2C(=CN1)C=COC3
Reaction #53624
titled compound
収率 79.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1=CCCN(C)C1
Reaction #63429
Arecoline
DOI: 10.6084/m9.figshare.5104873.v1
Nn1[nH]c(=O)c2ccccc2c1=O.[Na]
Reaction #70240
2-amino-1,2,3,4-tetrahydro-1,4-phthalazinedione sodium salt
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(COC(=O)C23Cc4cnn(-c5ccc(F)cc5)c4C=C2CCN(S(=O)(=O)c2ccc(N4CCOCC4)nc2)C3)no1
Reaction #173984
DOI: 10.1039/C8SC04228D
CN(C)CC1CCCN1C(=O)C(Cc1ccccc1)N(C)C(=O)C(Cc1ccc2ccccc2c1)N(C)C(=O)C=CCC(C)(C)NC(=O)OC(C)(C)C
Reaction #173998
DOI: 10.1039/C8SC04228D
Cc1nc(N2CCC=C(C(N)=O)C2)c2c(C)c(C)n(-c3c(C(C)C)csc3C)c2n1
Reaction #183044
DOI: 10.1039/C8SC04228D
CC12Cn3cnc(-c4ccc(F)cc4)c3C=C1CCCC2C(=O)c1ccc(C(=O)O)s1
Reaction #186462
DOI: 10.1039/C8SC04228D
CN(C(=O)C(Cc1ccc2ccccc2c1)N(C)C(=O)C=CCC(C)(C)NC(=O)OC(C)(C)C)C(CNC(=S)NC1CC1)Cc1ccccc1
Reaction #186924
DOI: 10.1039/C8SC04228D
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