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5203

Cc1ccc(C(=O)ON2C(=O)CCC2=O)cc1
Reaction #3765
4-toluic acid succinimidyl ester
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C(=O)ON2C(=O)CCC2=O)cc1
Reaction #3767
4-toluic acid succinimidyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(/C=C\c2cc(OC)c(OC)c(OC)c2)cc1O
Reaction #8837
combretastatin A-4
DOI: 10.6084/m9.figshare.5104873.v1
CON(Cc1cc(C(=O)NOCCO)c(Nc2ccc(I)cc2F)c(F)c1F)C(=O)C(C)C
Reaction #49047
3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(isobutyryl-methoxy-amino)-methyl]-benzamide
Выход 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](COCc1ccccc1)C(=O)N[C@@H](CC(N)=O)C(=O)O
Reaction #50733
Boc-Ser(Bzl)-Asn-OH
Выход 71.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](COCc1ccccc1)C(=O)N[C@@H](CCC(=O)OCc1ccccc1)C(=O)O
Reaction #54608
Boc-Ser(Bzl)-Glu(OBzl)-OH
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCOc1ccc2c(c1)C(C#CC1CC1)(C(F)(F)F)OC(=O)N2)ON1C(=O)CCC1=O
Reaction #57295
12
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)NC(OC2CCCCC2)[C@H](O)[C@H](Cc2ccccc2)NC(=O)O[C@H]2CCOC2)cc1
Reaction #57456
white solid
Выход 67.5%DOI: 10.6084/m9.figshare.5104873.v1
CCC(C)OC(NS(=O)(=O)c1ccc(OC)cc1)[C@H](O)[C@H](Cc1ccccc1)NC(=O)O[C@H]1CCOC1
Reaction #57460
(3S)tetrahydro-3-furanyl N-((1S,2R)-1-benzyl-3-sec-butoxy[(4-methoxyphenyl)sulfonyl]amino-2-hydroxypropyl)carbamate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H](Cc1ccccc1)[C@H](O)CC(OC1CCCC1)S(=O)(=O)c1ccc2nccnc2c1)O[C@H]1CCOC1
Reaction #57466
(3S)tetrahydro-3-furanyl N-[(1S,2R)-1-benzyl-4-(cyclopentyloxy)-2-hydroxy-4-(6-quinoxalinyl sulfonyl)butyl]carbamate
Выход 86.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)C(C)c2ccccc2)c(C(=O)O)c1
Reaction #58307
5-methoxy-2-(2-phenylpropionyl)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCC[C@H](N)C1
Reaction #58615
(S)-3-amino-azepane-1-carboxylic acid tert-butyl ester
Выход 54.3%DOI: 10.6084/m9.figshare.5104873.v1
CON(C)C(=O)C(Cc1ccc(Cl)cc1)n1nnc2ccccc21
Reaction #58663
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CON(C)C(=O)[C@@H](NC(=O)OCc1ccccc1)C(C)C
Reaction #72420
desired compound
Выход 87.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@@H](C=O)NC(=O)OCc1ccccc1
Reaction #72421
aldehyde
Выход 99.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCC(=O)ON1C(=O)CCC1=O)Nc1cccc(B(O)O)c1
Reaction #82908
N-(3-dihydroxyboryl-phenyl)succinamic acid, succinimidyl ester
Выход 59.4%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #84844
product
Выход 23.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)/C=C/CC[C@H](NC(=O)OC(C)(C)C)C(=O)Nc1cccn(CC(=O)O)c1=O
Reaction #86601
(S,E)-2-(3-(2-(tert-butoxycarbonylamino)-7-methoxy-7-oxohept-5-enamido)-2-oxopyridin-1(2H)-yl)acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)[C@H](CC1CCNC1=O)NC(=O)OC(C)(C)C
Reaction #87106
tert-butyl ((2S)-4-methyl-3-oxo-1-(2-oxopyrrolidin-3-yl)pent-4-en-2-yl)carbamate
Выход 42.7%DOI: 10.6084/m9.figshare.5104873.v1
CON(C)C(=O)[C@H](CC1CCCCC1)NC(=O)OC(C)(C)C
Reaction #87110
(S)-tert-Butyl (3-cyclohexyl-1-(methoxy(methyl)amino)-1-oxopropan-2-yl)carbamate
Выход 105.2%DOI: 10.6084/m9.figshare.5104873.v1
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