بحث البنية الفرعية

CC(C)(C)CC=O

CC(C)(C)OC(=O)CC(=O)C[C@@H](CC#N)O[Si](C)(C)C(C)(C)C
Reaction #5779
(R)-1,1-dimethylethyl 6-cyano-5-[(1,1-dimethylethyl)dimethylsilyl]oxy-3-oxohexanoate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[C@H](N)C(N)=O
Reaction #6425
tertiary leucine amide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(CCO)CCO
Reaction #7102
3,3-dimethyl-1,5-pentanediol
DOI: 10.6084/m9.figshare.5104873.v1
CCC(C)(C)C(=O)C(=O)N1CCCC1C(=O)NNc1ccccn1
Reaction #7999
1-(3,3-Dimethyl-2-oxo-pentanoyl)-pyrrolidine-2-carboxylic acid N′-pyridine-2-yl-hydrazide
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(=O)NC1=O
Reaction #42859
3,3-dimethylpyrrolidin-2,5-dione
المردود 89.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(O)C12CC3CC(CC(C3)C1)C2
Reaction #46044
α-hydroxytricyclo[3.3.1.13,7]decane-1-acetic acid, methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(=O)C12CC3CC(CC(O)(C3)C1)C2
Reaction #46045
Formula 1a
DOI: 10.6084/m9.figshare.5104873.v1
C=CC(C)(C)C(N)C(=O)OC
Reaction #51455
methyl 2(R/S)-amino-3,3-dimethyl-4-pentenoate
المردود 75.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CNC(C(=O)OC)(C(C)(C)NC(=O)OCc1ccccc1)S(=O)(=O)c1ccc(Oc2ccc(F)cc2)cc1
Reaction #51456
methyl 2(R/S)-[4-(4-fluorophenoxy)benzenesulfonyl][(ethoxycarbonyl)methyl]amino-3-(benzyloxycarbonyl)amino-3-methylbutanoate
المردود 75.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(O)C12CC3CC(CC(C3)C1)C2
Reaction #57411
a-hydroxytricyclo[3.3.1.13,7]decane-1-acetic acid, methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](N)C(C)(C)C.Cl
Reaction #81111
title compound
المردود 92.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC[C@@H]1C[C@H]1OC(=O)N[C@H](C(=O)O)C(C)(C)C.C[C@H](N)c1ccccc1
Reaction #88820
VII
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #90152
crude product
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(C(C)(C)C(=O)CC(=O)OC(C)(C)C)n1
Reaction #90173
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC(C(=O)N1CC2(CC2)CC1c1ncc(-c2ccc(-c3ccc4cc(-c5cnc(C6CC(C#N)CN6C(=O)C(NC(=O)OC)C(C)(C)C)[nH]5)ccc4c3)cc2)[nH]1)C(C)C
Reaction #159159
title compound
المردود 48.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC(C(=O)N1CC2(CC2)CC1c1ncc(-c2ccc3cc(-c4ccc(-c5cnc(C6CC(C#N)CN6C(=O)C(NC(=O)OC)C(C)(C)C)[nH]5)cc4)ccc3c2)[nH]1)C(C)C
Reaction #159163
title compound
المردود 45.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[C@H](N)C(=O)O
Reaction #164023
L-tert-leucine
المردود 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[C@@H](N)C(=O)O
Reaction #164024
D-tert-leucine
المردود 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(N)C(=O)O
Reaction #164025
DL-tert-leucine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[C@@H](N)C(=O)O
Reaction #164026
D-tert-leucine
المردود 92.0%DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي