Recherche de Sous-structure

410805

Cl.OC[C@H]1CCCCN1
Reaction #88578
title compound
Rendement 100.4%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #159050
residue
Rendement 19.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCC1C(=O)OCC(=O)c1ccc2c(c1)CCc1cc(C(=O)COC(=O)C3C4CCC(C4)N3C(=O)OC(C)(C)C)ccc1-2
Reaction #159083
2-aza-bicyclo[2.2.1]heptane-2,3-dicarboxylic acid 3-(2-{7-[2-(1-tert-butoxycarbonyl-pyrrolidine-2-carbonyloxy)-acetyl]-9,10-dihydro-phenanthren-2-yl}-2-oxo-ethyl) ester 2-tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCC1C(=O)OCC(=O)c1ccc2c(c1)oc1cc(C(=O)COC(=O)C3C4CCC(C4)N3C(=O)OC(C)(C)C)ccc12
Reaction #159092
2-Aza-bicyclo[2.2.1]heptane-2,3-dicarboxylic acid 3-(2-{7-[2-(1-tert-butoxycarbonyl-pyrrolidine-2-carbonyloxy)-acetyl]-dibenzofuran-3-yl}-2-oxo-ethyl) ester 2-tert-butyl ester
Rendement 93.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(F)(F)CC1C(=O)O
Reaction #162082
1-(tert-butoxycarbonyl)-4,4-difluoropiperidine-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #167000
residue
Rendement 19.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCC1C(=O)OCC(=O)c1ccc2c(c1)CCc1cc(C(=O)COC(=O)C3C4CCC(C4)N3C(=O)OC(C)(C)C)ccc1-2
Reaction #167029
2-aza-bicyclo[2.2.1]heptane-2,3-dicarboxylic acid 3-(2-{7-[2-(1-tert-butoxycarbonyl-pyrrolidine-2-carbonyloxy)-acetyl]-9,10-dihydro-phenanthren-2-yl}-2-oxo-ethyl)ester 2-tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCC1C(=O)OCC(=O)c1ccc2c(c1)oc1cc(C(=O)COC(=O)C3C4CCC(C4)N3C(=O)OC(C)(C)C)ccc12
Reaction #167038
2-Aza-bicyclo[2.2.1]heptane-2,3-dicarboxylic acid 3-(2-{7-[2-(1-tert-butoxycarbonyl-pyrrolidine-2-carbonyloxy)-acetyl]-dibenzofuran-3-yl}-2-oxo-ethyl) ester 2-tert-butyl ester
Rendement 93.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC(n2ncc(COc3ccc(-n4cnnn4)nc3)n2)CCN1C(=O)OC(C)(C)C
Reaction #167849
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC(N=[N+]=[N-])CCN1C(=O)OC(C)(C)C
Reaction #178439
DOI: 10.1039/C8SC04228D
COc1ccc(-c2cnc(Nc3cnc(C)c(NC(=O)C4CCCCN4C(=O)OC(C)(C)C)c3)nc2)cc1
Reaction #183999
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CC2CC2C1C=O
Reaction #186016
DOI: 10.1039/C8SC04228D
CCC1CCCC(C(O)C(Cc2ccccc2)N(Cc2ccccc2)Cc2ccccc2)N1C(=O)OC(C)(C)C
Reaction #187160
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCCCC1COc1cccc(COS(C)(=O)=O)n1
Reaction #195952
DOI: 10.1039/C8SC04228D
COC(C(=O)OC1(C2CCCCN2C(=O)OC(C)(C)C)CN(C(=O)OCc2ccccc2)C1)(c1ccccc1)C(F)(F)F
Reaction #196382
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1C2CC(CC2O)C1C(=O)OCc1ccccc1
Reaction #197243
DOI: 10.1039/C8SC04228D
Cc1c(-c2ccc(F)cc2)nnc(N2CCC(N(C)C(=O)C3CCCCN3C(=O)OC(C)(C)C)CC2)c1C
Reaction #205642
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)C1CCC(c2cc(N)n3nccc3n2)CN1C(=O)OC(C)(C)C
Reaction #208953
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCCCC1C1(O)CNC1
Reaction #211456
DOI: 10.1039/C8SC04228D
COC(=O)C1CC(CCC#N)CCN1C(=O)OC(C)(C)C
Reaction #223205
DOI: 10.1039/C8SC04228D
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