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NC1CCCc2sccc21

CC(=O)NC1CCC(=O)c2sccc21
Reaction #174911
DOI: 10.1039/C8SC04228D
CC(=O)c1cc2c(s1)CCCC2NC(N)=O
Reaction #182911
DOI: 10.1039/C8SC04228D
O=CNC1CCC(=O)c2sccc21
Reaction #183464
DOI: 10.1039/C8SC04228D
NC(=O)NC1CCC(=O)c2sccc21
Reaction #193528
DOI: 10.1039/C8SC04228D
O=C(NC1CCCc2sccc21)N1CCOCC1
Reaction #196257
DOI: 10.1039/C8SC04228D
COCNC(=O)NC1CCC(=O)c2sccc21
Reaction #198531
DOI: 10.1039/C8SC04228D
Cl
Reaction #202372
DOI: 10.1039/C8SC04228D
CC(C)Cc1ccc(-c2nc(-c3cc4c(s3)CCCC4N3CC(C(=O)O)C3)no2)cc1
Reaction #203381
DOI: 10.1039/C8SC04228D
CC1CCc2sccc2C1N
Reaction #211244
DOI: 10.1039/C8SC04228D
CC(=O)NC1CCC(=O)c2sccc21
Reaction #214202
N-(4,5,6,7-tetrahydro-7-oxobenzo[b]thien-4-yl)acetamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC1CCC(=O)c2sccc21
Reaction #214203
title product
Ausbeute 73.6%DOI: 10.6084/m9.figshare.5104873.v1
[C-]#[N+]C1CCC(=O)c2sccc21
Reaction #223993
DOI: 10.1039/C8SC04228D
NC(=O)NC1CCCc2sccc21
Reaction #233625
DOI: 10.1039/C8SC04228D
CC(=O)NC1CCC(=O)c2sccc21
Reaction #244659
DOI: 10.1039/C8SC04228D
NC1CCCc2sc(Br)cc21
Reaction #250307
DOI: 10.1039/C8SC04228D
CNC(=O)NC1CCC(OC)c2sccc21
Reaction #266503
DOI: 10.1039/C8SC04228D
N#Cc1cc2c(s1)CCCC2NC=O
Reaction #272955
DOI: 10.1039/C8SC04228D
O=C1CCC(N=C=S)c2ccsc21
Reaction #287101
DOI: 10.1039/C8SC04228D
CNC(=O)NC1CCCc2sccc21
Reaction #290411
DOI: 10.1039/C8SC04228D
O=C=NC1CCC(=O)c2sccc21
Reaction #295846
DOI: 10.1039/C8SC04228D
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