子结构搜索

437056

CCOC(=O)CNC(=O)C(NC(=O)OC(C)(C)C)C(C)(C)SC(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #259518
DOI: 10.1039/C8SC04228D
CC(C)(S)CNC(=O)OC(C)(C)C
Reaction #264855
DOI: 10.1039/C8SC04228D
COc1ccc(CSC(C)(C)[C@@H](N)C(=O)O)cc1
Reaction #411468
desired product
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #700398
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(SCc1cccc(Oc2ccccc2)c1)[C@H](N)C(=O)N1C[C@@H](F)C[C@H]1C#N.Cl
Reaction #806854
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(CCN(CCCCCN)CC(C)(C)SC(c1ccccc1)(c1ccccc1)c1ccccc1)CC(C)(C)SC(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #911761
DOI: 10.1039/C8SC04228D
CCCCOC(=O)NC(C(=O)OC)C(C)(C)SCc1ccc(-c2ccc(-c3cccc4c3oc3ccccc34)cc2)cc1
Reaction #987562
desired product
收率 72.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](NC(=O)OC(C)(C)C)C(C)(C)SC(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #1284183
N-t-butoxycarbonyl-S-trityl-D-penicillamine methyl ester
收率 97.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CNC(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)(C)SC(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #1284184
N-t-butoxycarbonyl-S-trityl-L-penicillamylglycine ethyl ester
收率 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CNC(=O)[C@@H](N)C(C)(C)SC(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #1284185
S-trityl-L-penicillamylglycine ethyl ester
收率 102.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(SC(c1ccccc1)(c1ccccc1)c1ccccc1)[C@H](N)C(=O)N[C@@H](Cc1ccc(S(=O)(=O)O)cc1)C(=O)O
Reaction #1284187
S-trityl-L-penicillamyl-p-sulfophenylalanine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(SC(c1ccccc1)(c1ccccc1)c1ccccc1)C(N)C(=O)NC(Cc1ccc(S(=O)(=O)O)cc1)C(=O)O
Reaction #1305294
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N(CCN(CCCCCN)CC(C)(C)SC(c1ccccc1)(c1ccccc1)c1ccccc1)CC(C)(C)SC(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #1544688
N1 -(t-butoxycarbonyl)-N1,N4 -bis [2-methyl-2-(triphenylmethylthio)propyl ]-1,4,10-triazadecane
收率 68.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CSC(C)(C)C(NC(=O)OC(C)(C)C)C(=O)N2CCC(C)CC2)cc1
Reaction #1547595
Compound ( 29 )
收率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CSC(C)(C)C(N)C(=O)N2CCC(C)CC2)cc1
Reaction #1547596
Compound ( 30 )
收率 109.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](C(=O)NCC(=O)O)C(C)(C)SC(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #1768336
desired title material
DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)NC(C(=O)OC)C(C)(C)SCc1ccc(-c2ccc(-c3cccc4c3oc3ccccc34)cc2)cc1
Reaction #1869859
desired product
收率 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(CCN(CCCCCN)CC(C)(C)SC(c1ccccc1)(c1ccccc1)c1ccccc1)CC(C)(C)SC(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #2375098
N1 -(t-butoxycarbonyl)-N1,N4 -bis(2-methyl-2-(triphenylmethylthio)propyl]-1,4,10-triazadecane
收率 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(S)CNC(=O)OC(C)(C)C
Reaction #2381863
tert-butyl [2-methyl-2-mercaptopropyl]carbamate
收率 94.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CNC(=O)C(N)C(C)(C)SC(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #2429088
DOI: 10.1039/C8SC04228D
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