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C#CC(C)C

COC1(C#CCO)CCOCC1
Reaction #50178
4-methoxy-4-(3-hydroxyprop-1-ynyl)tetrahydropyran
Выход 47.6%DOI: 10.6084/m9.figshare.5104873.v1
COC1(/C=C/CO)CCOCC1
Reaction #50179
4-methoxy-4-(3-hydroxy -trans-prop-1-enyl)tetrahydropyran
Выход 48.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C)CC#C[C@H]1CC[C@H](NC)CC1
Reaction #53861
trans-{4-[3-(Allyl-methyl-amino)-prop-1-ynyl]-cyclohexyl}-methyl-amine
Выход 107.6%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C)CC#C[C@H]1CC[C@H](N(C)C(=O)Oc2ccc(Cl)cc2)CC1
Reaction #53862
trans-{4-[3-(Allyl-methyl-amino)-prop-1-ynyl]-cyclohexyl}-methyl-carbamic acid 4-chloro-phenyl ester
Выход 67.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(CCCC2SCC(=O)N2C/C=C\C2(O)CCCCC2)cc1
Reaction #56496
title product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(CCCC2SCC(=O)N2CCCC2(O)CCCCC2)cc1
Reaction #56497
title product
DOI: 10.6084/m9.figshare.5104873.v1
COCCOCOc1ccc(NC(=O)OC(C)(C)C)c(C(O)(C#CC2CC2)C(F)(F)F)c1
Reaction #57290
7
Выход 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(Oc1cc(Cl)cc(Cl)c1)C(=O)NC(C)(C)C#CCCCCl
Reaction #57499
required product
Выход 97.8%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(C#CC2(N)CCCCC2)nc(-c2ccccc2)c1-c1nc2c(N)ncnc2s1
Reaction #60890
title compound
Выход 41.0%DOI: 10.6084/m9.figshare.5104873.v1
CCSCC(C)(OC)c1cc2cc([N+](=O)[O-])c(C(F)(F)F)cc2n1S(C)(=O)=O
Reaction #61209
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C#CC(C)(CSCC)OC
Reaction #61210
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCC(C(=O)N(c2cc(C#CC(C)(C)C)sc2C(=O)O)N(C)C2CCNCC2)CC1
Reaction #67588
title compound
Выход 0.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(C#CC(C)C)c(N)c1
Reaction #68336
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)Nc1cc([N+](=O)[O-])ccc1C#CC(C)C
Reaction #68396
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C#CC(C)C)c([N+](=O)[O-])c1
Reaction #68408
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NCc1nnc2ccc(-c3cc(C4CC4)on3)nn12
Reaction #68673
title compound
Выход 23.2%DOI: 10.6084/m9.figshare.5104873.v1
CC#CC(CC(=O)O)c1ccc(OCN2C(=O)C(C)(C)c3cc(C(F)(F)F)ccc32)cc1
Reaction #68763
3-[4-(3,3-dimethyl-2-oxo-5-trifluoromethyl-2,3-dihydroindol-1-ylmethoxy)phenyl]hex-4-ynoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC#CC(CC(=O)O)c1ccc(OCn2c(=O)sc3ccccc32)cc1
Reaction #68766
3-[4-(2-oxobenzothiazol-3-ylmethoxy)-phenyl]hex-4-ynoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC#CC(CC(=O)O)c1ccc(OCN2C(=O)C(C)(C)Oc3ccccc32)cc1
Reaction #68767
3-[4-(2,2-dimethyl-3-oxo-2,3-dihydrobenzo[1,4]oxazin-4-ylmethoxy)phenyl]hex-4-ynoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(O)C#Cc1cc(Br)cnc1N
Reaction #69782
4-(2-amino-5-bromo-pyridin-3-yl)-2-methyl-but-3-yn-2-ol
Выход 82.0%DOI: 10.6084/m9.figshare.5104873.v1
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