部分構造検索

454991

C[C@@H](O)[C@H]1C(=O)N2C(C(=O)O)=C(S[C@@H]3CN[C@H](c4csc(N)n4)C3)[C@H](C)[C@H]12
Reaction #65562
(4R,5S,6S)-3-[(2S,4S)-2-(2-aminothiazol-4-yl) -pyrrolidin-4-ylthio]-6-[(1R)-1-hydroxyethyl]-4-methyl-7-oxo-1-azabicyclo [3.2.0]hept-2-ene-2-carboxylic acid
収率 45.7%DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2ccc(C(=O)O)cc2)COc2cc(O)ccc2C1CCCCCCCCCS(=O)CCCC(F)(F)C(F)(F)F
Reaction #179181
DOI: 10.1039/C8SC04228D
COCOc1ccc(C2(C)COc3cc(OCOC)ccc3C2CCCNCCCCCS(=O)CCCC(F)(F)C(F)(F)F)cc1
Reaction #183684
DOI: 10.1039/C8SC04228D
O=C1CNCC2=C1C(c1ccc(F)c(Br)c1)C1=C(CCCS1(=O)=O)N2
Reaction #189928
DOI: 10.1039/C8SC04228D
O=C(CCCCCSC1=CC(OC2CCCCO2)CC1=O)Oc1ccccc1
Reaction #223645
DOI: 10.1039/C8SC04228D
CCCCSC1(c2ccc(-c3ccccc3)cc2)CC(C(=O)OC)N(C(=O)OCc2ccccc2)C1
Reaction #230670
DOI: 10.1039/C8SC04228D
[I-]
Reaction #232571
DOI: 10.1039/C8SC04228D
C=CCOC(=O)C1=C(SC2CC(CC[n+]3cn(C)cc3COC)N(C(=O)OCC=C)C2)C(C)C2C(C(C)O)C(=O)N12
Reaction #237255
DOI: 10.1039/C8SC04228D
C=CCOC(=O)C1=C(SC2CC(CC[n+]3cc(CC(N)=O)n(C)c3)N(C(=O)OCC=C)C2)C(C)C2C(C(C)O)C(=O)N12
Reaction #240715
DOI: 10.1039/C8SC04228D
CN(C)CCC1(C)SCCC2=C1Cc1ccccc12
Reaction #260099
DOI: 10.1039/C8SC04228D
CC1(c2ccc(C(=O)O)cc2)COc2cc(O)ccc2C1CCCCCCCCCSCCCC(F)(F)C(F)(F)F
Reaction #287313
DOI: 10.1039/C8SC04228D
COCOc1ccc(C2(C)COc3cc(OCOC)ccc3C2CCCOc2ccc(CCCSCCCC(F)(F)C(F)(F)F)cc2)cc1
Reaction #295505
DOI: 10.1039/C8SC04228D
COC(=O)CCCSC1N=C2C=CC=CN2C1Cc1cccc2ccccc12
Reaction #303151
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCSC1N=C2C=CC=CN2C1Cc1cccc2ccccc12
Reaction #303152
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)C1=C(SC2CC(COCCNC(N)=O)N(C(=O)OCC=C)C2)C(C)C2C(C(C)O)C(=O)N12
Reaction #373920
DOI: 10.1039/C8SC04228D
[I-]
Reaction #391913
DOI: 10.1039/C8SC04228D
CC1(c2ccncc2)COc2cc(O)ccc2C1CCCCCCCCCS(=O)CCCC(F)(F)C(F)(F)F
Reaction #406753
DOI: 10.1039/C8SC04228D
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)O)=C(S[C@@H]3CN[C@H](CSC(F)F)C3)[C@H](C)[C@H]12
Reaction #433560
(4R,5S,6S)-3-[(2S,4S)-2-(difluoromethyl)thiomethylpyrrolidin-4-ylthio]-6-[(1R)-1-hydroxyethyl]-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid
収率 58.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)O)=C(S[C@@H]3CN[C@H](CSCC(N)=O)C3)[C@H](C)[C@H]12
Reaction #433561
(4R,5S,6S)-3-[(2S,4S)-2-(carbamoylmethyl)thiomethylpyrrolidin-4-ylthio]-6-[(1R)-1-hydroxyethyl]-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid
収率 66.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(=N)N1C[C@@H](SC2=C(C(=O)O)N3C(=O)[C@H]([C@@H](C)O)[C@H]3[C@H]2C)C[C@H]1COCCO
Reaction #433562
(4R,5S,6S)-3-[(2S,4S)-1-acetimidoyl-2-(2-hydroxyethyloxymethyl)pyrrolidin-4-ylthio]-6-[(1R)-1-hydroxyethyl]- 4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid
収率 87.4%DOI: 10.6084/m9.figshare.5104873.v1
1 ページ次のページ