مشارك في 165 تفاعل

6446

CC(C)[N-]C(C)C.[Li+]
Reaction #1296
lithium diisopropylamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)[N-]C(C)C.[Li+]
Reaction #1432
lithium diisopropylamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cccc([C@@H](Oc2ccc3c(cnn3-c3ccc(F)cc3)c2)[C@H](C)NC(=O)C2CCCC2)c1
Reaction #41336
N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-(3-methoxyphenyl)propan-2-yl]cyclopentanecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)CO[C@H]1CN(C(=O)OC(C)(C)C)[C@@H]([C@@H](O)[C@H](Cc2cc(F)cc(F)c2)NC(=O)C2CCCC2)CO1
Reaction #48760
desired compound
المردود 98.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(O)C1(Cc2ccncc2)CCCC1
Reaction #81930
desired product
المردود 24.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=C(O)C1(Cc2ccncc2)CCCC1
Reaction #82509
desired product
المردود 24.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=C(O)C1CCCC1
Reaction #87845
cyclopentanecarboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@]2(C)[C@H]1OC(=O)COC(=O)C1CCCC1
Reaction #93009
above-identified compound
المردود 106.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
C=C(C)[C@@H]1CC[C@]2(NCCN3CCN(C(=O)C4CCCC4)CC3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)O)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172936
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(c1cccs1)C1CCCC1
Reaction #181404
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(C1CCCC1)N1CCC(N2CCC(N3C(=O)NC4CCCCC43)CC2)CC1
Reaction #182613
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)C(Cc1ccc(O)cc1)NC(=O)C1(NC(=O)C(SC(=O)C2CCCC2)C(C)C)CCCC1
Reaction #206441
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COCCn1c(=NC(=O)C2CCCC2)sc2ccccc21
Reaction #210457
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)C(CS)NC(=O)C1CCCC1
Reaction #234010
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(c1cccs1)C1CCCC1
Reaction #251478
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cn1c(COc2ccc(CC3SC(=O)NC3=O)cc2)nc2ccc(Oc3ccc(NC(=O)C4CCCC4)cc3)cc21
Reaction #299549
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(c1cccs1)C1CCCC1
Reaction #322276
crude product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
CC(C)[N-]C(C)C.[Li+]
Reaction #352165
lithium diisopropylamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
CC(C)(C)OC(=O)C(CCc1ccccc1)CC1(C(=O)O)CCCC1
Reaction #361416
1-(2-t-Butoxycarbonyl-4-phenylbutyl)cyclopentanecarboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_02
COC(=O)CC(=O)C1CCCC1
Reaction #370204
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
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