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1003144

COC(C)(C)C(NC(=O)OC(C)(C)C)C(=O)O
Reaction #159228
2-tert-Butoxycarbonylamino-3-methoxy-3-methyl-butyric acid
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC(C(=O)O)C(C)(C)OC
Reaction #159229
3-Methoxy-2-methoxycarbonylamino-3-methyl-butyric acid
Выход 65.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(C)(C)C(NC(=O)OC(C)(C)C)C(=O)O
Reaction #167170
2-tert-Butoxycarbonylamino-3-methoxy-3-methyl-butyric acid
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(C)(C)C(NC(=O)OC(C)(C)C)C(=O)O
Reaction #368599
DOI: 10.1039/C8SC04228D
COC(C)(C)C(NC(=O)OC(C)(C)C)C(=O)O
Reaction #372078
DOI: 10.1039/C8SC04228D
COC(=O)NC(C(=O)O)C(C)(C)OC
Reaction #379438
DOI: 10.1039/C8SC04228D
COC(C)(C)C(NC(=O)OC(C)(C)C)C(=O)O
Reaction #504920
2-tert-Butoxycarbonylamino-3-methoxy-3-methyl-butyric acid
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC(C(=O)O)C(C)(C)OC
Reaction #504921
3-Methoxy-2-methoxycarbonylamino-3-methyl-butyric acid
Выход 65.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(C)(C)[C@@H](NC(=O)OC(C)(C)C)C(=O)O
Reaction #1124678
(R)-2-((tert-butoxycarbonyl)amino)-3-methoxy-3-methylbutanoic acid
Выход 88.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(C)(C)[C@@H](NC(=O)OC(C)(C)C)C(=O)NNC(=N)c1cc(F)ccc1F
Reaction #1124679
(R)-tert-butyl (1-(2-((2,5-difluorophenyl)(imino)methyl)hydrazinyl)-3-methoxy-3-methyl-1-oxobutan-2-yl)carbamate
Выход 15.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(C)(C)C(NC(=O)OC(C)(C)C)C(=O)O
Reaction #1249493
title compound
Выход 82.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(C)(C)C(NC(=O)OC(C)(C)C)C(=O)N1CCC(N2Cc3cnc(C)n3C2=O)CC1
Reaction #1249494
title compound
Выход 99.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(C)(C)C(NC(=O)OC(C)(C)C)C(=O)O
Reaction #1273133
2-tert-Butoxycarbonylamino-3-methoxy-3-methyl-butyric acid
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC(C(=O)O)C(C)(C)OC
Reaction #1273134
3-Methoxy-2-methoxycarbonylamino-3-methyl-butyric acid
Выход 65.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(C)(C)C(N)c1nc2cc(-c3ccc(C#N)cc3)ccc2[nH]1
Reaction #1511357
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(NC(=O)OC(C)(C)C)=C1CSCSC1
Reaction #1534939
Ethyl α-tert.-butoxycarbonylamino-(4,5-dihydro-1,3-dithiin-5-ylidene)-acetate
Выход 70.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(C)(C)[C@H](NC(=O)OC(C)(C)C)C(=O)O
Reaction #1558234
title compound
Выход 43.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N[C@H](C(=O)O)C(C)(C)OC
Reaction #1558235
title compound
Выход 71.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(C)(C)C(NC(=O)OC(C)(C)C)C(=O)N1CCC(N2Cc3cnc(C)n3C2=O)CC1
Reaction #1661343
DOI: 10.1039/C8SC04228D
COC(C)(C)C(NC(=O)OC(C)(C)C)C(=O)O
Reaction #2126474
2-tert-Butoxycarbonylamino-3-methoxy-3-methyl-butyric acid
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1
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