Recherche de Sous-structure

CCOCCN

C=CCOC(=O)[C@@H](CCc1ccccc1)NC(=O)OC(C)(C)C
Reaction #2009
N-(t-Butoxycarbonyl)-D-homophenylalanine allyl ester
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)[C@H](N)CCc1ccccc1
Reaction #2010
D-Homophenylalanine allyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)COc1ccc(CN2C(=O)COC3(CCNCC3)C2Cc2ccc(F)cc2)cc1
Reaction #40650
5-(4-fluorobenzyl)-4-(4-isobutoxybenzyl)-1-oxa-4,9-diaza-spiro[5.5]undecan-3-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(Oc2ccc3c(c2)cc(C(=O)N2CCOCC2)n3Cc2ccccc2)CC1
Reaction #48121
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1N[C@@H]([C@H](OCc2ccccc2)[C@H](Cc2cc(F)cc(F)c2)N(Cc2ccccc2)Cc2ccccc2)COC1O
Reaction #48692
desired compound
Rendement 99.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1N[C@@H]([C@H](OCc2ccccc2)[C@H](Cc2cc(F)cc(F)c2)N(Cc2ccccc2)Cc2ccccc2)CO[C@H]1OCC(C)(C)C
Reaction #48693
desired compound
Rendement 56.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1N[C@@H]([C@@H](OCc2ccccc2)[C@H](Cc2cc(F)cc(F)c2)N(Cc2ccccc2)Cc2ccccc2)CO[C@H]1OCC1(F)CCCCC1
Reaction #48708
title compound
Rendement 31.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1N[C@@H]([C@H](OCc2ccccc2)[C@H](Cc2cc(F)cc(F)c2)N(Cc2ccccc2)Cc2ccccc2)CO[C@H]1OCC(C)(CF)CF
Reaction #48733
desired compound
Rendement 42.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(OC(c2ccccc2)C2CC(O)CN2C(=O)CCCCCN)c2ccc(OC)cc2)cc1
Reaction #49172
compound 5
Rendement 91.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCC1(C)CCc2c(C)c(OCCOC(=O)NCCCCCC(=O)N3CC(O)CC3C(OC(c3ccc(OC)cc3)c3ccc(OC)cc3)c3ccccc3)c(C)c(C)c2O1
Reaction #49176
Compound 19
Rendement 88.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(OC(c2ccccc2)C2CC(O)CN2CCCCCCN)c2ccc(OC)cc2)cc1
Reaction #49181
compound 31
Rendement 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCNC(=O)CCC(C)C1CCC2C3CCC4CC(OC(=O)NCCCCCC(=O)N5CC(O)CC5C(OC(c5ccc(OC)cc5)c5ccc(OC)cc5)c5ccccc5)CCC4(C)C3CCC12C
Reaction #49209
Compound 90
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(C(=O)OCC)N1C(=O)c2ccccc2C1=O
Reaction #54591
ethyl α-phthalimidopentanoate
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O.CC(=O)O.COc1ccccc1CC(N)(Cc1ccccc1OC)C1CN(Cc2ccccc2)CCO1
Reaction #58610
80
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)c1csc(NC(=O)[C@@H](NC(=O)[C@H](N)c2ccc(OCCN3CCOCC3)cc2)[C@@H](C)c2ccccc2)n1
Reaction #61100
(2S,3S)-2-{(R)-2-amino-2-[4-(2-morpholin-4-yl-ethoxy)-phenyl]-acetylamino}-3-phenyl-N-(4-propionyl-thiazol-2-yl)-butyramide
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #61101
solid
Rendement 29.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(=O)n(-c2ccc(N3CCOCC3)c(F)c2)c(CCCOc2cccc(F)c2)n1
Reaction #84532
title compound
Rendement 49.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cn([C@H]2C[C@H](O)[C@@H](CNC(=O)N(C)N=O)O2)c(=O)[nH]c1=O
Reaction #93937
white fine needles
Rendement 70.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(=S)N[C@@]1(c2cc(Br)ccc2F)CO[C@@H](COCc2ccccc2)C[C@H]1CO)c1ccccc1
Reaction #155595
product
Rendement 63.8%DOI: 10.6084/m9.figshare.5104873.v1
COC[C@@H](C)NCc1ccc(F)c([C@]23CO[C@@H](c4cnn(C)c4)C[C@H]2CSC(N)=N3)c1
Reaction #155619
product
DOI: 10.6084/m9.figshare.5104873.v1
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