部分構造検索

427332

CC(C)(C)OC(=O)NC1CCC2=C(C=CC(Br)(C(O)c3cccnc3)C2)C1
Reaction #50410
2-tert.Butoxycarbonylamino-6-bromo-1,2,3,4-tetrahydronaphth-6-yl-3-pyridylmethanol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCc2cc(C=O)ccc2C1
Reaction #60358
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCC2=C(C=CC(Br)(C(O)c3cccnc3)C2)C1
Reaction #574515
2-tert.Butoxycarbonylamino-6-bromo-1,2,3,4-tetrahydronaphth-6-yl-3-pyridylmethanol
DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1ccc2c(c1)CC[C@@H](NC(=O)OC(C)(C)C)C2
Reaction #834247
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCc2cc(C=O)ccc2C1
Reaction #889196
DOI: 10.1039/C8SC04228D
C=CCN(C(=O)OC(C)(C)C)[C@@H]1CCc2cc(Br)ccc2C1
Reaction #957531
product
収率 73.7%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C(=O)OC(C)(C)C)[C@@H]1CCc2cc(NS(=O)(=O)c3ccc(C(C)C)cc3)ccc2C1
Reaction #957532
crude product
収率 115.5%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C(=O)OC(C)(C)C)[C@H]1CCc2cc(Br)ccc2C1
Reaction #957533
product
収率 71.6%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C(=O)OC(C)(C)C)[C@H]1CCc2cc(NS(=O)(=O)c3ccc(C(C)C)cc3)ccc2C1
Reaction #957534
crude product
収率 177.4%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C(=O)OC(C)(C)C)[C@H]1CCc2cc(N(C)S(=O)(=O)c3ccc(C(C)C)cc3)ccc2C1
Reaction #957535
crude product
収率 112.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(C(=O)OC(C)(C)C)[C@H]1CCc2cc(Br)ccc2C1
Reaction #957559
title compound
収率 76.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(C(=O)OC(C)(C)C)[C@H]1CCc2cc(Br)ccc2C1
Reaction #957570
product
収率 76.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)NCc1ccc2c(c1)CCC(N)C2
Reaction #1781476
desired compound
DOI: 10.6084/m9.figshare.5104873.v1