参与 46 个反应

CCC#C

CC/C=C\CCCCCC/C=C/CCOC(C)=O
Reaction #2040
(3E,11Z)-3,11-tetradecadien-1-yl acetate
收率 15.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#Cc1ccccc1S(N)(=O)=O
Reaction #6476
2-(but-1-yn-1-yl)-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCC#Cc1ccccn1
Reaction #9274
title compound
收率 84.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCC#Cc1cc(OC)ccn1
Reaction #9282
2-(1-butynyl)-4-methoxypyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCC#Cc1ccc(F)cc1N
Reaction #244208
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCC#Cc1ccc(F)cc1OCOC
Reaction #287454
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCC#Cc1cc(Cl)ncc1NC(=O)OC(C)(C)C
Reaction #378787
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCC#Cc1ccccn1
Reaction #435006
title compound
收率 84.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
CCC#CC1(C(F)(F)F)OC(=O)Nc2ccc(OC)cc21
Reaction #450532
4-(1-butynyl)-6-methoxy-4-trifluoromethyl-1,4-dihydro-2H-3,1-benzoxazin-2-one
收率 48.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
CCc1cc(-c2cnc(Cl)c(Cl)c2)no1
Reaction #455475
desired product
收率 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
CCC#CC1(C(F)(F)F)OC(=O)Nc2ccc(OC)cc21
Reaction #457541
4-(1-butynyl)-6-methoxy-4-trifluoromethyl-1,4-dihydro-2H-3,1-benzoxazin-2-one
收率 48.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
CCC#CC1(C(F)(F)F)OC(=O)Nc2ccc(OC)cc21
Reaction #468135
4-(1-butynyl)-6-methoxy-4-trifluoromethyl-1,4-dihydro-2H-3,1-benzoxazin-2-one
收率 48.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
CCC#Cc1ccc(F)cc1OCOC
Reaction #510361
title compound
收率 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
CCC#Cc1cc(Cl)ncc1NC(=O)OC(C)(C)C
Reaction #600259
tert-butyl 4-(but-1-ynyl)-6-chloropyridin-3-ylcarbamate
收率 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
CCc1cc2cc(S(C)(=O)=O)cc(I)c2o1
Reaction #605753
title compound
收率 48.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
CCC#Cc1cncc(Br)c1
Reaction #626474
title compound
收率 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
CCc1cc2cc(S(C)(=O)=O)cc(I)c2o1
Reaction #663019
title compound
收率 48.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
CCC#Cc1cc(C(=O)OC)ccn1
Reaction #915727
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CCC#CC1(C(F)(F)F)OC(=O)Nc2ccc(OC)cc21
Reaction #916387
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CCC#Cc1cc(OC(F)(F)F)cc2c1OC(C(F)(F)F)C(C(=O)OCC)=C2
Reaction #942098
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_08
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