Substructure Search

381838

CCCC(N)C(O)C(=O)NC1CC1
Reaction #176047
DOI: 10.1039/C8SC04228D
CCCC(NC(=O)OC(C)(C)C)C(O)C(=O)NC1CC1
Reaction #382546
DOI: 10.1039/C8SC04228D
CCCC(N)C(O)C(=O)NC1CC1
Reaction #393138
DOI: 10.1039/C8SC04228D
CCCC(NC(=O)OC(C)(C)C)C(O)C(=O)NC1CC1
Reaction #402971
DOI: 10.1039/C8SC04228D
CCCC(N)C(OC)(OC)C(=O)NC1CC1
Reaction #616467
amine
DOI: 10.6084/m9.figshare.5104873.v1
CCC[C@H](NC(=O)OC(C)(C)C)C(OCC)(OCC)C(=O)NC1CC1
Reaction #616471
(S)-tert-butyl 1-(cyclopropylamino)-2,2-diethoxy-1-oxohexan-3-ylcarbamate
Yield 35.6%DOI: 10.6084/m9.figshare.5104873.v1
CCC[C@H](N)C(OCC)(OCC)C(=O)NC1CC1
Reaction #616472
(3S)-3-Amino-N-cyclopropyl-2,2-diethoxyhexanamide
Yield 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC(CC1CCC1)C(O)C(=O)NC1CC1
Reaction #922876
DOI: 10.1039/C8SC04228D
Cl
Reaction #925345
DOI: 10.1039/C8SC04228D
CCCC(NC(=O)OC(C)(C)C)C(O)C(=O)NC1CC1
Reaction #1310768
DOI: 10.1039/C8SC04228D
CCCC(N)C(O)C(=O)NC1CC1
Reaction #1326478
DOI: 10.1039/C8SC04228D
CCC[C@H](NC(=O)OC(C)(C)C)C(O)C(=O)NC1CC1
Reaction #1598634
tert-butyl (3S)-1-(cyclopropylamino)-2-hydroxy-1-oxohexan-3-ylcarbamate
Yield 88.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC(C(=O)NC1CC1)[C@H](CC1CCC1)NC(=O)OC(C)(C)C
Reaction #1598636
(3S)-3-(tert-butoxycarbonylamino)-4-cyclobutyl-1-(cyclopropylamino)-1-oxobutan-2-yl acetate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](CC1CCC1)C(O)C(=O)NC1CC1
Reaction #1598637
tert-butyl (2S)-1-cyclobutyl-4-(cyclopropylamino)-3-hydroxy-4-oxobutan-2-ylcarbamate
Yield 86.8%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@H](CC1CCC1)C(O)C(=O)NC1CC1.O=C(O)C(F)(F)F
Reaction #1598641
(3S)-3-amino-4-cyclobutyl-N-cyclopropyl-2-hydroxy-butanamide trifluoroacetic acid salt
DOI: 10.6084/m9.figshare.5104873.v1
CCC[C@H](NC(=O)OC(C)(C)C)[C@H](O)C(=O)NC1CC1
Reaction #2015882
(2S,3S)—N-Cyclopropyl-3-(tert-butoxycarbonyl)amino-2-hydroxyhexanoic acid amide
DOI: 10.6084/m9.figshare.5104873.v1
CCC[C@H](N)[C@H](O)C(=O)NC1CC1.Cl
Reaction #2015883
(2S,3S)—N-cyclopropyl-3-amino-2-hydroxyhexanoic acid amide hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CCC[C@H](NC(=O)OC(C)(C)C)[C@H](O)C(=O)NC1CC1
Reaction #2015884
(2S,3S)—N-cyclopropyl-3-(tert-butoxycarbonyl)amino-2-hydroxyhexanoic acid amide
DOI: 10.6084/m9.figshare.5104873.v1
CCC[C@H](NC(=O)OC(C)(C)C)[C@H](O)C(=O)NC1CC1
Reaction #2015886
(2S,3S)—N-cyclopropyl-3-(tert-butoxycarbonyl)amino-2-hydroxyhexanoic acid amide
DOI: 10.6084/m9.figshare.5104873.v1
CCC[C@H](N)[C@H](O)C(=O)NC1CC1.Cl
Reaction #2015887
(2S,3S)—N-cyclopropyl-3-amino-2-hydroxyhexanoic acid amide hydrochloride
Yield 80.2%DOI: 10.6084/m9.figshare.5104873.v1
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