Involved in 31 reactions

5429

COC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CCl
Reaction #1526
(2S,3S)-1-chloro-3-methoxycarbonylamino-4-phenyl-2-butanol
Yield 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CCl
Reaction #1527
(2S,3S)-1-chloro-3-methoxycarbonylamino-4-phenyl-2-butanol
Yield 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)N[C@@H](Cc1ccccc1)C(=O)CCl
Reaction #320520
methyl (S)-(1-benzyl-3-chloro-2-oxo-propyl)-carbamate
Yield 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
COC(=O)N[C@@H](Cc1ccccc1)C(=O)CCl
Reaction #320521
methyl (S)-(1-benzyl-3-chloro-2-oxo-propyl)-carbamate
Yield 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
COC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CCl
Reaction #320522
methyl (1S,2S)-(1-benzyl-3-chloro-2-hydroxy-propyl)-carbamate
Yield 90.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
COC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CCl
Reaction #320523
methyl (1S,2S)-(1-benzyl-3-chloro-2-hydroxy-propyl)-carbamate
Yield 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
COC(=O)N[C@@H](Cc1ccccc1)C(=O)CCl
Reaction #347093
methyl (S)-(1-benzyl-3-chloro-2-oxo-propyl)-carbamate
Yield 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_06
COC(=O)N[C@@H](Cc1ccccc1)C(=O)CCl
Reaction #347094
methyl (S)-(1-benzyl-3-chloro-2-oxo-propyl)carbamate
Yield 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_06
COC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CCl
Reaction #347095
methyl (1S,2S)-(1-benzyl-3-chloro-2-hydroxy- propyl)-carbamate
Yield 90.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_06
COC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CCl
Reaction #347096
methyl (1S,2S)-(1-benzyl-3-chloro-2-hydroxypropyl)-carbamate
Yield 89.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_06
COC(=O)N[C@@H](Cc1ccccc1)C(=O)CCl
Reaction #501172
(3S)-3-methoxycarbonylamino-1-chloro-4-phenyl-2-butanone
Yield 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
COC(=O)N[C@@H](Cc1ccccc1)C(=O)CCl
Reaction #1159062
(3S)-3-methoxycarbonylamino-1-chloro-4-phenyl-2-butanone
Yield 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_06
COC(=O)N[C@@H](Cc1ccccc1)C(=O)CCl
Reaction #1544463
methyl(S)-(1-benzyl-3-chloro-2-oxo-propyl)-carbamate
Yield 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_12
COC(=O)N[C@@H](Cc1ccccc1)C(=O)CCl
Reaction #1544464
methyl(S)-(1-benzyl-3-chloro-2-oxo-propyl)-carbamate
Yield 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_12
COC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CCl
Reaction #1544465
methyl(1S,2S)-(1-benzyl-3-chloro-2-hydroxy-propyl)-carbamate
Yield 90.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_12
COC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CCl
Reaction #1544466
methyl(1S,2S)-(1-benzyl-3-chloro-2-hydroxy-propyl)-carbamate
Yield 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_12
COC(=O)N[C@@H](Cc1ccccc1)C(=O)CCl
Reaction #1688905
methyl (S)-(1-benzyl-3-chloro-2-oxo-propyl)-carbamate
Yield 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_11
COC(=O)N[C@@H](Cc1ccccc1)C(=O)CCl
Reaction #1688906
methyl (S)-(1-benzyl-3-chloro-2-oxo-propyl)-carbamate
Yield 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_11
COC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CCl
Reaction #1688907
methyl (1S,2S)-(1-benzyl-3-chloro-2-hydroxy-propyl)-carbamate
Yield 90.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_11
COC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CCl
Reaction #1688908
methyl (1S,2S)-(1-benzyl-3-chloro 2-hydroxy-propyl)-carbamate
Yield 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_11
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