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1321363

COCC(C)(O)c1ccc2c(n1)N1[C@H](C2)CN(C(=O)OC(C)(C)C)C[C@H]1C
Reaction #12050
(4R,9aR)-6-(1-(RS)-Hydroxy-2-methoxy-1-methyl-ethyl)-4-methyl-3,4,9,9a-tetrahydro-1H-2,4a,5-triaza-fluorene-2-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(CC(=O)OCC)n1ccc2cc(OCCc3ccc4c(n3)N(C(=O)OC(C)(C)C)CCC4)ccc21
Reaction #52277
title compound
Ausbeute 13.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCc2ccc(CCO)nc21
Reaction #52279
7-(2-hydroxy-ethyl)-3,4-dihydro-2H-[1,8]naphthyridine-1-carboxylic acid tert-butyl ester
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(c1ccccc1)n1ccc2cc(OCCc3ccc4c(n3)N(C(=O)OC(C)(C)C)CCC4)ccc21
Reaction #52280
title compound
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(c1cccc(OCc2ccccc2)c1)n1ccc2cc(OCCc3ccc4c(n3)N(C(=O)OC(C)(C)C)CCC4)ccc21
Reaction #52284
title compound
Ausbeute 493.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=C(c1cccc(C)c1)n1ccc2cc(OCCc3ccc4c(n3)N(C(=O)OC(C)(C)C)CCC4)ccc21
Reaction #52286
title compound
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #52287
E/Z isomeric mixture
Ausbeute 35.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=C(c1ccc(-c2ccccc2)cc1)n1ccc2cc(OCCc3ccc4c(n3)N(C(=O)OC(C)(C)C)CCC4)ccc21
Reaction #52288
title compound
Ausbeute 8.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=C(c1ccccc1OC)n1ccc2cc(OCCc3ccc4c(n3)N(C(=O)OC(C)(C)C)CCC4)ccc21
Reaction #52291
title compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=C(c1cccc(OC)c1)n1ccc2cc(OCCc3ccc4c(n3)N(C(=O)OC(C)(C)C)CCC4)ccc21
Reaction #52292
title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=C(c1ccc(OC)cc1)n1ccc2cc(OCCc3ccc4c(n3)N(C(=O)OC(C)(C)C)CCC4)ccc21
Reaction #52293
title compound
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC(c1cnc2ccccc2c1)n1ccc2cc(OCCc3ccc4c(n3)NCCC4)ccc21
Reaction #52294
title compound
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=C(c1cccc(Cl)c1)n1ccc2cc(OCCc3ccc4c(n3)N(C(=O)OC(C)(C)C)CCC4)ccc21
Reaction #52295
title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=C(c1ccc2ccccc2c1)n1ccc2cc(OCCc3ccc4c(n3)N(C(=O)OC(C)(C)C)CCC4)ccc21
Reaction #52297
title compound
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C=C(c1ccccc1Cl)n1ccc2cc(OCCc3ccc4c(n3)N(C(=O)OC(C)(C)C)CCC4)ccc21
Reaction #52298
title compound
Ausbeute 43.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=C(c1cccc2ccccc12)n1ccc2cc(OCCc3ccc4c(n3)N(C(=O)OC(C)(C)C)CCC4)ccc21
Reaction #52299
title compound
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C=C(c1ccc(F)cc1)n1ccc2cc(OCCc3ccc4c(n3)N(C(=O)OC(C)(C)C)CCC4)ccc21
Reaction #52300
title compound
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=C(c1ccc2c(c1)CCO2)n1ccc2cc(OCCc3ccc4c(n3)N(C(=O)OC(C)(C)C)CCC4)ccc21
Reaction #52301
title compound
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C#Cc1ccc2c(c1)OCO2
Reaction #52304
title compound
Ausbeute 54.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=C(c1ccc2c(c1)OCO2)n1ccc2cc(OCCc3ccc4c(n3)N(C(=O)OC(C)(C)C)CCC4)ccc21
Reaction #52305
title compound
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1
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