cyclen

CC(C)(C)OC(=O)CN1CCNCCN(CC(=O)OC(C)(C)C)CCN(CC(=O)OC(C)(C)C)CC1
Reaction #65327
1,4,7,10-Tetraazacyclododecane-4,7,10-triacetic acid tri-t-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
C1CN2CCN3CCN(CCN1)C23
Reaction #94498
1,4,7,10-tetraazatricyclo[5.5.1.04,13 ]tridecane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
O=C(Nc1ccccc1)N1CCNCCNCCNCC1
Reaction #181904
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C1CN2CCN3CC[N+](=C23)CCN1
Reaction #233319
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C1CN2CCN3CCN(CCN1)P23
Reaction #346668
1,4,7,10-tetraaza-13-phosphatricyclo[5.5.1.04,13 ]tridecane
Выход 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_07
C1CN2CCN3CCN(CCN1)P23
Reaction #346669
1,4,7,10Tetraaza-13-phosphatricyclo[5.5.1.04,13 ]tridecane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_07
COc1ccc([N+](=O)[O-])cc1CN1CCNCCNCCNCC1
Reaction #354103
N-(2-methoxy-5-nitrobenzyl)-1,4,7,10-tetraazacyclododecane
Выход 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
O=[N+]([O-])c1ccc(CN2CCNCCNCCNCC2)cc1
Reaction #354104
title product
Выход 88.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
C1CN2CCN3CCN(CCN1)C23
Reaction #370099
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=CN1CCNCCNCCNCC1
Reaction #401254
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
C1CN2CCN3CCN(CCN1)P23
Reaction #405456
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(OCc1ccccc1)C(CCCN1C(=O)c2ccccc2C1=O)N1CCNCCNCCNCC1
Reaction #470377
product
Выход 81.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CCCCCCCCCCCCC
Reaction #563971
tridecane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_12
CC(C)(C)OC(=O)CN1CCNCCNCCNCC1
Reaction #567729
desired compound
Выход 99.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_11
O=C(O)C(CCC(C(=O)O)N1CCNCCNCCNCC1)N1CCNCCNCCNCC1
Reaction #706092
title product
Выход 51.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_09
O=C(O)C(C(C(=O)O)N1CCNCCNCCNCC1)N1CCNCCNCCNCC1
Reaction #706096
title product
Выход 16.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_09
O=C(CN1CCNCCNCCNCC1)NCc1nc2ccccc2c2ccccc12
Reaction #805924
product 10
Выход 47.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
O=[N+]([O-])c1ccc(CN2CCNCCNCCNCC2)cc1
Reaction #919999
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CCCCCCCCCCCCC
Reaction #985263
tridecane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_04
COc1ccc([N+](=O)[O-])cc1CN1CCNCCNCCNCC1
Reaction #1234517
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
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