بحث البنية الفرعية

465638

CCOC(=O)C1C2CCCCC2CCN1C(=O)OC
Reaction #1690
title compound
المردود 95.2%DOI: 10.6084/m9.figshare.5104873.v1
CCC(C)C(NC(=O)c1ccccc1S[SH](CCC(=O)O)NC(C)=O)C(=O)O
Reaction #3841
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(F)(F)C(C)(C)[C@H]1C(=O)O
Reaction #11266
(2S)-4,4-Difluoro-3,3-dimethyl-N-(Boc)proline
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)[C@@H](C(=O)NCC(F)(F)F)NCC1(F)F
Reaction #11269
(2S)-4,4-difluoro-3,3-dimethyl-pyrrolidine-2-carboxylic acid (2,2,2-trifluoro-ethyl)-amide
المردود 107.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(C)NCC2CCCCC21.Cl
Reaction #52160
1-methyl-octahydroisoindole-1-carboxylic acid, methyl ester hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
N[C@@H](CCC(=O)O)C(=O)O
Reaction #58019
L-glutamic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@H](N)C(=O)O
Reaction #61371
L-isoleucine
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)O[C@H](C)[C@H]1C(=O)N(Cc2ccc(OC)cc2)[C@@H]1C(=O)OC(C)(C)C
Reaction #62560
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@H](NC(=O)C(CSC(C)=O)C(F)(F)F)C(=O)O
Reaction #64785
(S)-N-[2-[(acetylthio)methyl]-3,3,3-trifluoro-1-oxopropyl]-L-isoleucine
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@H](NC(=O)C(CSC(C)=O)C(F)(F)F)C(=O)O
Reaction #64804
(S)-N-[2-[(acetylthio)methyl]-3,3,3-trifluoro-1-oxopropyl]-L-isoleucine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1Nc2cc(Cl)cc(Cl)c2C2c3ccccc3CCC12
Reaction #75646
Compound 12
المردود 85.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1Nc2c(Cl)cc(Cl)c(Cl)c2C2OCCC12
Reaction #75693
Compound 67
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1Nc2ccccc2C[C@@H]1C
Reaction #80793
cis-2-methoxycarbonyl-3-methyltetrahydroquinoline
المردود 78.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1Nc2ccccc2C[C@@H]1C
Reaction #80794
cis-2-methoxycarbonyl-3-methyltetrahydroquinoline
المردود 47.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@H](NC(=O)OCc1ccc([N+](=O)[O-])cc1)C(=O)O
Reaction #83095
desired product
المردود 24.5%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@H](N)CN[C@H](C(=O)OC)[C@H](CSC)C(=O)C1NCCc2ccccc21
Reaction #83386
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@H](NC(=O)OC)C(=O)O
Reaction #84037
(2S,3S)-2-(methoxycarbonylamino)-3-methylpentanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](C)[C@H](NC(=O)OC)C(=O)O
Reaction #84043
(2S,3R)-2-(methoxycarbonylamino)-3-methylpentanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCCN(C(=O)OCc2ccccc2)C1C(=O)O
Reaction #89160
crude residue
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CCCN[C@H]1CN1C(=O)c2ccccc2C1=O
Reaction #89241
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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