部分構造検索

1218927

N[C@H]1CC[C@@H](NS(=O)(=O)c2ccc(-c3ccc(F)cc3F)cc2)CC1
Reaction #156757
title compound
収率 25.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(N[C@H]1CC[C@@H](NCC(F)(F)F)CC1)c1ccc(-c2ccc(F)cc2F)cc1
Reaction #156758
oil
収率 79.2%DOI: 10.6084/m9.figshare.5104873.v1
CCN(C)C1CCC(NS(=O)(=O)c2ccc(-c3ccc(F)cc3F)cc2)CC1
Reaction #180165
DOI: 10.1039/C8SC04228D
O=C(O)C(CCCN1C(=O)c2ccccc2C1=O)NS(=O)(=O)c1ccc(-c2ccc(Cl)cc2)cc1
Reaction #233012
DOI: 10.1039/C8SC04228D
COc1ccc(-c2ccc(S(=O)(=O)NC(CC(O)CNc3ccccc3)C(=O)O)cc2)cc1
Reaction #247741
DOI: 10.1039/C8SC04228D
NCCCCNS(=O)(=O)c1ccc(-c2ccc(Br)cc2)cc1
Reaction #262040
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)C(CCCN1C(=O)c2ccccc2C1=O)NS(=O)(=O)c1ccc(-c2ccc(Cl)cc2)cc1
Reaction #383206
DOI: 10.1039/C8SC04228D
CC(=O)NCCCCNS(=O)(=O)c1ccc(-c2ccccc2)cc1
Reaction #387790
DOI: 10.1039/C8SC04228D
NCCCCNS(=O)(=O)c1ccc(-c2ccccc2)cc1
Reaction #405207
DOI: 10.1039/C8SC04228D
COc1ccc(-c2ccc(S(=O)(=O)NC3CC(CNc4ccccc4)OC3=O)cc2)cc1
Reaction #500552
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2ccc(S(=O)(=O)NC(CC(O)CNc3ccccc3)C(=O)O)cc2)cc1
Reaction #500553
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2ccc(S(=O)(=O)NC(CC(O)CNc3ccccc3)C(=O)O)cc2)cc1
Reaction #500555
2-[(4′-Methoxy[1,1′-biphenyl]-4-yl)sulfonyl]amino-4-hydroxy-5-(phenylamino)-pentanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
N[C@H]1CC[C@@H](NS(=O)(=O)c2ccc(-c3ccc(F)cc3F)cc2)CC1
Reaction #710567
title compound
収率 25.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(N[C@H]1CC[C@@H](NCC(F)(F)F)CC1)c1ccc(-c2ccc(F)cc2F)cc1
Reaction #710568
oil
収率 79.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)[C@@H](CCCN1C(=O)c2ccccc2C1=O)NS(=O)(=O)c1ccc(-c2ccc(Cl)cc2)cc1
Reaction #738503
(2R)-(4′-chlorobiphenyl-4-sulfonylamino)-5-(1,3-dioxo-1,3-dihydroisoindol-2-yl)pentanoic acid t-butyl ester
収率 53.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@@H](CCCN1C(=O)c2ccccc2C1=O)NS(=O)(=O)c1ccc(-c2ccc(Cl)cc2)cc1
Reaction #738504
(2R)-(4′-chlorobiphenyl-4-sulfonylamino)-5-(1,3-dioxo-1,3-dihydroisoindol-2-yl)pentanoic acid
収率 97.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NOC(c1ccccc1)(c1ccccc1)c1ccccc1)[C@@H](CCCN1C(=O)c2ccccc2C1=O)NS(=O)(=O)c1ccc(-c2ccc(Cl)cc2)cc1
Reaction #738505
(2R)-(4′-chlorobiphenyl-4-sulfonylamino)-5-(1,3-dioxo-1,3-dihydroisoindol-2-yl)pentanoic acid O-tritylhydroxyamide
収率 64.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NO)[C@@H](CCCN1C(=O)c2ccccc2C1=O)NS(=O)(=O)c1ccc(-c2ccc(Cl)cc2)cc1
Reaction #738506
(2R)-(4′-chlorobiphenyl-4-sulfonylamino)-5-(1,3-dioxo-1,3-dihydroisoindol-2-yl)pentanoic acid hydroxyamide
収率 82.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccccc1C(=O)NCCC[C@@H](NS(=O)(=O)c1ccc(-c2ccc(Cl)cc2)cc1)C(=O)O
Reaction #738507
(4R)-N-[4-(4′-chlorobiphenyl-4-sulfonylamino)-4-carboxybutyl]phthalamic acid
収率 62.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(NC1CCC(NCC(F)(F)F)CC1)c1ccc(-c2ccc(F)cc2F)cc1
Reaction #749639
DOI: 10.1039/C8SC04228D
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