(S)-2-phthalimido-6-hydroxyhexanoic acid

CCCC[C@@H](C(=O)NCC(=O)OCC)N1C(=O)c2ccccc2C1=O
Reaction #1288
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(OCc1ccccc1)[C@H](CCCCO)N1C(=O)c2ccccc2C1=O
Reaction #1293
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)[C@H](CCCCO)N1C(=O)c2ccccc2C1=O
Reaction #1294
title product
수율 196.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCC[C@@H](C(=O)NCC(=O)OCC)N1C(=O)c2ccccc2C1=O
Reaction #1422
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(OCc1ccccc1)[C@H](CCCCO)N1C(=O)c2ccccc2C1=O
Reaction #1429
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)[C@H](CCCCO)N1C(=O)c2ccccc2C1=O
Reaction #1430
title product
수율 196.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCC[C@@H](C(=O)NCC(=O)OCC)N1C(=O)c2ccccc2C1=O
Reaction #352156
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
O=C(OCc1ccccc1)[C@H](CCCCO)N1C(=O)c2ccccc2C1=O
Reaction #352162
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
COC(=O)[C@H](CCCCO)N1C(=O)c2ccccc2C1=O
Reaction #352163
title product
수율 196.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
CCCC[C@@H](C(=O)NCC(=O)OCC)N1C(=O)c2ccccc2C1=O
Reaction #429435
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
O=C(OCc1ccccc1)[C@H](CCCCO)N1C(=O)c2ccccc2C1=O
Reaction #429441
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
COC(=O)[C@H](CCCCO)N1C(=O)c2ccccc2C1=O
Reaction #429442
title product
수율 196.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
CCCC[C@@H](C(=O)NCC(=O)OCC)N1C(=O)c2ccccc2C1=O
Reaction #429453
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
O=C(OCc1ccccc1)[C@H](CCCCO)N1C(=O)c2ccccc2C1=O
Reaction #429457
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
COC(=O)[C@H](CCCCO)N1C(=O)c2ccccc2C1=O
Reaction #429458
title product
수율 196.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
CCCC[C@@H](C(=O)NCC(=O)OCC)N1C(=O)c2ccccc2C1=O
Reaction #430225
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
O=C(OCc1ccccc1)[C@H](CCCCO)N1C(=O)c2ccccc2C1=O
Reaction #430231
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
COC(=O)[C@H](CCCCO)N1C(=O)c2ccccc2C1=O
Reaction #430232
title product
수율 196.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
O=CCCC[C@@H](C(=O)O)N1C(=O)c2ccccc2C1=O
Reaction #630389
5-Formyl-2(S)-phthalimidopentanoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_04
O=C(OCc1ccccc1)[C@H](CCCCO)N1C(=O)c2ccccc2C1=O
Reaction #630390
benzyl 6-hydroxy-2(S)-phthalimidohexanoate
수율 198.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_04
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