Hydroxylamine-O-sulfonic acid

Cc1cc(CO)c2ccccc2n1
Reaction #89711
4-hydroxymethyl-2-methyl quinoline
收率 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)(C)OC(=O)NCC1=CC=C2C(=[C+]1)C(C)(C)C1=CC(CC#N)=CCN21.[O-][Cl+3]([O-])([O-])[O-]
Reaction #164001
2-(tert-Butoxycarbonylamino-methyl)-8-cyanomethyl-10,10-dimethyl-10H-pyrido[1,2-a]indolylium perchlorate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C1NC2CC3CC1CN(C3)C2
Reaction #167598
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCCCCCCCCCCCCCCC(=O)C1C(=O)CC(C#N)CC1=O
Reaction #177633
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NS(=O)(=O)c1ccc(C2=C(c3ccc(F)cc3)CC3(CC3)C2)cc1
Reaction #188515
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CS(=O)(=O)c1ccc(-n2cc(C#N)nc2-c2ccc(Cl)cc2)cc1
Reaction #189617
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cncc(-c2nc(C(F)(F)F)cn2-c2ccc(S(N)(=O)=O)cc2)c1
Reaction #199810
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#Cc1c(Cl)ccc(Br)c1F
Reaction #201570
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(O)Cc1cn(N)c2ccc(F)cc12
Reaction #213266
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NS(=O)(=O)c1cc2c(s1)S(=O)(=O)NN=C2
Reaction #215755
2H-Thieno[3,2-e]-1,2,3-thiadiazine-6-sulfonamide 1,1-dioxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CC1=NNS(=O)(=O)c2sc(S(N)(=O)=O)cc21
Reaction #215757
4-Methyl-2H-thieno[3,2-e]-1,2,3-thiadiazine-6-sulfonamide 1,1-dioxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
N#CCc1ccc([N+](=O)[O-])c2ccoc12
Reaction #221142
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Nn1ccc2cc(OCc3ccccc3)ccc21
Reaction #225255
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
NS(=O)(=O)c1ccc(C2=C(c3ccc(F)c(Cl)c3)CCC2)cc1
Reaction #227716
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
N#Cc1cc(F)c(Br)cc1F
Reaction #232477
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CN(C)S(=O)(=O)c1cn(N)c2ccc(F)cc12
Reaction #234856
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1onc(-c2ccc(S(N)(=O)=O)cc2)c1-c1ccccc1
Reaction #240927
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCc1c(OC)c(OC)cc(S(N)(=O)=O)c1C(=O)N(C)C
Reaction #243487
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cn1nc2ccccc2c1S(N)(=O)=O
Reaction #249469
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCc1c(OC)c(OC)cc(S(N)(=O)=O)c1C(=O)N(CC)CC
Reaction #250290
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
上一页第 2 页下一页