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376990

C#C[C@@H]1CCCN1C(=O)OC(C)(C)C
Reaction #45451
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)CC[C@@H]2C#Cc2ccc(Cl)c(OC)n2)c(OC)c1
Reaction #157717
title compound
Выход 52.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(C#C[C@H]2CCC(=O)N2)ccc1Cl
Reaction #157718
title compound
Выход 82.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)CC[C@@H]2C#Cc2ccc(C(C)(C)C)cc2)c(OC)c1
Reaction #157725
(5R)-5-[(4-tert-butylphenyl)ethynyl]-1-(2,4-dimethoxybenzyl)pyrrolidin-2-one
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)/[C](=C/[C@H]1CCC(=O)N1Cc1ccc(OC)cc1OC)c1ccc(C(C)(C)C)cc1
Reaction #157726
title compound
Выход 96.0%DOI: 10.6084/m9.figshare.5104873.v1
C#CC1COC(C)(C)N1C(=O)OC(C)(C)C
Reaction #178403
DOI: 10.1039/C8SC04228D
C#CC(C)N(C)C=Nc1cnc(Oc2ccc(Cl)c(C(F)(F)F)c2)cc1C
Reaction #181154
DOI: 10.1039/C8SC04228D
C#CC1CCC(C(N)=O)N1C(=O)C(CC(C)C)NC(=O)OC(C)(C)C
Reaction #183786
DOI: 10.1039/C8SC04228D
C#CC1CCC(C#N)N1C(=O)CNC1CCCC1
Reaction #184628
DOI: 10.1039/C8SC04228D
C#CC(C)(C)N1CCC(OC(=O)N(CC)c2ccccc2OC)N(c2nnc(C(F)(F)F)s2)C1=O
Reaction #188335
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCCC1C#Cc1cncnc1
Reaction #200319
DOI: 10.1039/C8SC04228D
C#CC(NC(=O)OC(C)(C)C)C(C)O
Reaction #203812
DOI: 10.1039/C8SC04228D
C#CC1CCC(C#N)N1C(=O)CNC1(CO)CCCC1
Reaction #206499
DOI: 10.1039/C8SC04228D
C#CC1CCC(C(N)=O)N1C(=O)CCl
Reaction #209290
DOI: 10.1039/C8SC04228D
C#CC1CCC(C#N)N1C(=O)CNC1CCCC1O
Reaction #227952
DOI: 10.1039/C8SC04228D
CC#CC1CCC(C#N)N1C(=O)CCl
Reaction #231643
DOI: 10.1039/C8SC04228D
C#CC1CCC(C#N)N1C(=O)CNC1CCN(c2ccccn2)CC1
Reaction #244789
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1C(CCc2cccc(C(F)(F)F)n2)COC1(C)C
Reaction #249130
DOI: 10.1039/C8SC04228D
C#CC1CCC(C#N)N1C(=O)CNC(C)(C)C
Reaction #250154
DOI: 10.1039/C8SC04228D
COC(=O)C1CCC(C#C[Si](C)(C)C)N1
Reaction #265590
DOI: 10.1039/C8SC04228D
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