sodium periodate

C[C@@H]1COS(=O)(=O)N1c1ccccn1
Reaction #990
(R)-4-methyl-3-(2-pyridyl)-[1,2,3]oxathiazolidine-2,2-dioxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)C1=C(COCC=O)NC(C)=C(C(=O)OC)C1c1ccccc1Cl
Reaction #1346
title compound
收率 97.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)OC(=O)Cn1c(=O)n(C)c(=O)n(-c2cc(N3C(=O)C4CS(=O)CCN4C3=O)c(F)cc2Cl)c1=O
Reaction #1570
title product
收率 60.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C#CCOc1cc(-n2nc(CCC=O)[nH]c2=O)c(Cl)cc1Cl
Reaction #2061
title product
收率 92.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CS(=O)Cc1ccc(C(=O)c2ccc(Cl)cc2)cc1
Reaction #2196
desired product
收率 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C[C@@H]1C[C@@H](C(=O)O)N(C(=O)OC(C)(C)C)C1=O
Reaction #2977
product
收率 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(C)CCC(C)(C)c2cc(S(=O)Cc3ccc(C(=O)O)cc3)ccc21
Reaction #6613
title compound
收率 39.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=CCn1cnc2ccccc21
Reaction #7221
2-(benzimidazol-1-yl)-ethanal
收率 41.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C=C1[C@H](O[Si](C)(C)C(C)(C)C)CC(=O)C[C@H]1O[Si](C)(C)C(C)(C)C
Reaction #10261
(3R,5R)-3,5-Bis[(tert-butyldimethylsilyl)oxy]-4-methylenecyclohexanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=CCCCN1CCCCCCC1=O
Reaction #10276
4-(2-oxo-azocan-1-yl)-butyraldehyde
收率 0.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=CCOc1ccccc1
Reaction #41355
subtitle compound
收率 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=Cc1cc2c(nn1)OCCC2
Reaction #43429
product
收率 54.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=Cc1cc2c(nn1)OCCS2
Reaction #43431
solid
收率 36.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=Cc1cc2c(nn1)SCCO2
Reaction #43433
solid
收率 31.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=Cc1cc2c(nn1)OCCO2
Reaction #43450
solid
收率 64.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=Cc1cc2c(nn1)OCC2
Reaction #43458
product
收率 20.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN1CCc2ccc(C=O)cc2C1=O
Reaction #43635
product
收率 74.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1c(C=O)c(F)c2oc(C3CC3)nc2c1C#N
Reaction #45739
compound
收率 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(OCc1ccccc1)N1CCC(n2c(=O)[nH]c3nnccc32)CC1
Reaction #48363
product
收率 6.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CS(=O)CCN1C[C@H](c2cccc(F)c2F)CC[C@@H](NC(=O)OC(C)(C)C)C1=O
Reaction #48416
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
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