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1226375

N[C@@H]1CCC(c2ccc(O)cc2)CNC1=O
Reaction #48397
(3R)-3-Amino-6-(4-hydroxyphenyl)azepan-2-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCC(c2ccc(O)cc2)CC[C@H]1NC(=O)N1CCC(n2c(=O)[nH]c3ncccc32)CC1
Reaction #48433
title compound
Выход 33.5%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@H]1CCC(c2ccc(O)cc2)CNC1=O
Reaction #359095
(3R)-3-Amino-6-(4-hydroxyphenyl)azepan-2-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCC(c2ccc(O)cc2)CC[C@H]1NC(=O)N1CCC(n2c(=O)[nH]c3ncccc32)CC1
Reaction #359127
title compound
Выход 33.5%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@H]1CCC(c2ccc(O)cc2)CNC1=O
Reaction #580811
(3R)-3-Amino-6-(4-hydroxyphenyl)azepan-2-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCC(c2ccc(O)cc2)CC[C@H]1NC(=O)N1CCC(n2c(=O)[nH]c3ncccc32)CC1
Reaction #580846
title compound
Выход 33.5%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@H]1CCC(c2ccc(O)cc2)CNC1=O
Reaction #588299
(3R)-3-Amino-6-(4-hydroxyphenyl)azepan-2-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCC(c2ccc(O)cc2)CC[C@H]1NC(=O)N1CCC(n2c(=O)[nH]c3ncccc32)CC1
Reaction #588334
title compound
Выход 33.5%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@H]1CCC(c2ccc(O)cc2)CNC1=O
Reaction #1054727
(3R)-3-Amino-6-(4-hydroxyphenyl)azepan-2-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCC(c2ccc(O)cc2)CC[C@H]1NC(=O)N1CCC(n2c(=O)[nH]c3ncccc32)CC1
Reaction #1054762
title compound
Выход 33.5%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@H]1CCC(c2ccc(O)cc2)CNC1=O
Reaction #1453169
(3R)-3-Amino-6-(4-hydroxyphenyl)azepan-2-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCC(c2ccc(O)cc2)CC[C@H]1NC(=O)N1CCC(n2c(=O)[nH]c3ncccc32)CC1
Reaction #1453203
title compound
Выход 33.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCC(c2ccc(O)cc2)CCC1NC(=O)N1CCC(n2c(=O)[nH]c3ncccc32)CC1
Reaction #1660230
DOI: 10.1039/C8SC04228D
N[C@@H]1CCC(c2ccc(O)cc2)CNC1=O
Reaction #1855391
(3R)-3-Amino-6-(4-hydroxyphenyl)azepan-2-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCC(c2ccc(O)cc2)CC[C@H]1NC(=O)N1CCC(n2c(=O)[nH]c3ncccc32)CC1
Reaction #1855423
title compound
Выход 33.5%DOI: 10.6084/m9.figshare.5104873.v1