子结构搜索

COCCCC#C

C#CCC1C(=O)N(C)OC1c1ccccc1

2-methyl-5-phenyl-4-propargylisoxazolin-3-one

收率 34.5%DOI: 10.6084/m9.figshare.5104873.v1

C#CCCCOC1CCCCO1

1-(Tetrahydopyran-2-yloxy)-4-pentyne

DOI: 10.6084/m9.figshare.5104873.v1

CCCCCC#CCCCOC1CCCCO1

title compound ( 15 )

收率 58.0%DOI: 10.6084/m9.figshare.5104873.v1

CC(=O)[O-].CC(=O)[O-].[Ni+2]

DOI: 10.6084/m9.figshare.5104873.v1

CC(=O)OCCCC#Cc1ccccc1S(N)(=O)=O

2-(5-acetoxy-pent-1-yn-1-yl)-benzenesulfonamide

DOI: 10.6084/m9.figshare.5104873.v1

OC1(C#CCOC2CCCCO2)CCOCC1

Reaction #50176

4-hydroxy-4-[3-(tetrahydropyran-2-yloxy)prop-1-ynyl]tetrahydropyran

收率 88.3%DOI: 10.6084/m9.figshare.5104873.v1

COC1(C#CCOC2CCCCO2)CCOCC1

Reaction #50177

4-methoxy-4-[3-(tetrahydropyran-2-yloxy)prop-1-ynyl]tetrahydropyran

收率 96.1%DOI: 10.6084/m9.figshare.5104873.v1

COC1(C#CCO)CCOCC1

Reaction #50178

4-methoxy-4-(3-hydroxyprop-1-ynyl)tetrahydropyran

收率 47.6%DOI: 10.6084/m9.figshare.5104873.v1

Reaction #162528

DOI: 10.6084/m9.figshare.5104873.v1

CCC(CC)(c1ccc(O)c(C)c1)c1ccc(C=CC2(O)CCOCC2)c(C)c1

Reaction #191434

DOI: 10.1039/C8SC04228D

C#CCCCOC(=O)NC(=O)C(c1ccccc1)c1ccccc1

Reaction #195122

DOI: 10.1039/C8SC04228D

CC(C)(C)OC(=O)C1C(C#CC(=O)OCC(Cl)(Cl)Cl)C1(C)C

Reaction #208497

DOI: 10.1039/C8SC04228D

C#CCC(CCCC)(O[Si](C)(C)C)C(OC)OC

Reaction #213890

DOI: 10.6084/m9.figshare.5104873.v1

CCCCC(C/C=[CH]/[Sn]([CH2]CCC)([CH2]CCC)[CH2]CCC)(O[Si](C)(C)C)C(OC)OC

Reaction #213891

DOI: 10.6084/m9.figshare.5104873.v1

C#CCC(CCCC)(O[Si](C)(C)C)C(OC)OC

Reaction #213919

DOI: 10.6084/m9.figshare.5104873.v1

CCCCC(C/C=[CH]/[Sn]([CH2]CCC)([CH2]CCC)[CH2]CCC)(O[Si](C)(C)C)C(OC)OC

Reaction #213920

DOI: 10.6084/m9.figshare.5104873.v1

COC(=O)CCC#CCCC(=O)c1ccco1

Reaction #228280

DOI: 10.1039/C8SC04228D

CCC#CCC(C)C(=O)CP(=O)(OC)OC

Reaction #236681

DOI: 10.1039/C8SC04228D

CC#CCCC(C)(O)C=CC1C(O)CC(=O)C1CCCCCCC(=O)O

Reaction #239614

DOI: 10.1039/C8SC04228D

C#CCCCOCCCO[Si](C)(C)C(C)(C)C

Reaction #262497

DOI: 10.1039/C8SC04228D

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