部分構造検索

P

COC(=O)c1cc(N2CCOCC2)cc2c1nc(C)n2Cc1cccc(C(F)(F)F)c1C
Reaction #582
収率 0.0%
O=[PH](O)CCCOCc1ccccc1
Reaction #1626
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(CCCCn1c(=O)c2c(ncn2CCCCP(=O)(OCC)OCC)n(C)c1=O)OCC
Reaction #2095
Diethyl 4-{7-[4-(diethoxyphosphoryl)butyl]-3-methylxanthin-1-yl}butyl-phosphonate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCP(Cl)CCCCC
Reaction #2454
chloro di-n-pentylphosphine
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](C(=O)N1CCOCC1)N1CC[C@H](N(Cc2ccoc2)S(=O)(=O)c2ccc3cc(Cl)ccc3c2)C1=O
Reaction #7400
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(Cl)cnnc2cc1OCc1ccncc1.Cl
Reaction #7572
4-chloro-6-methoxy-7-(4-pyridylmethoxy)cinnoline hydrochloride
収率 122.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1O[C@@H](CNc2ccon2)CN1c1ccc(N2CCOCC2)c(F)c1
Reaction #8238
oil
収率 331.2%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #8240
solid
収率 52.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1O[C@@H](CNc2ccon2)CN1c1ccc(-n2ccnc2)c(F)c1
Reaction #8243
desired product
収率 158.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C1O[C@@H](CNc2ccon2)CN1c1ccc(-n2cnc(CO)c2)c(F)c1
Reaction #8245
desired product
収率 13.9%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(-c2nn3c(c2-c2ccnc4ccccc24)OCC3)nc1
Reaction #8376
title compound
収率 74.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)COc1ccc(OCCc2cccs2)cc1C
Reaction #9749
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)COc1ccc(SCc2coc(-c3ccc(C(F)(F)F)cc3)c2)cc1C
Reaction #9785
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCCCN(CCCc1ccccc1)S(=O)(=O)c1cccc2cnccc12
Reaction #10587
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCCCOc1cccc2c(Cl)nccc12
Reaction #10597
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)O[C@H]2CC[C@@H](NC(=O)OC(C)(C)C)CC2)cc1
Reaction #10659
title compound
収率 96.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCC[PH+](CCCC)CCCC.c1ccc([B-](c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #42146
tri-n-butylphosphonium tetraphenylborate
収率 53.0%DOI: 10.6084/m9.figshare.5104873.v1
CCSCCOc1cc(C)c(-c2cccc(COc3ccc4c(c3)OC[C@H]4CC(=O)OC)c2)c(C)c1
Reaction #43918
title compound
収率 60.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@@H]1COc2cc(OCc3cccc(-c4c(C)cc(OCCCS(C)(=O)=O)cc4COC(C)=O)c3)ccc21
Reaction #43930
title compound
収率 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CSCCCOc1cc(C)c(Br)c(C)c1
Reaction #43938
title compound
収率 87.0%DOI: 10.6084/m9.figshare.5104873.v1
1 ページ次のページ