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Br.CCNC(=O)[C@@H]1CCCN1C(=O)[C@H](C)N

Reaction #75321

L-alanyl-L-proline ethylamide hydrobromide

Rendimiento 82.0%DOI: 10.6084/m9.figshare.5104873.v1

CCNC(=O)[C@@H]1CCCN1C(=O)[C@H](C)NC(=O)C(C)(C)C

Reaction #75322

N-pivaloyl-L-alanyl-L-proline ethylamide

Rendimiento 40.0%DOI: 10.6084/m9.figshare.5104873.v1

CCNC(=O)[C@@H]1CCCN1C(=O)[C@H](C)NC(=O)c1ccccc1

Reaction #75323

N-benzoyl-L-alanyl-L-proline ethylamide

Rendimiento 68.9%DOI: 10.6084/m9.figshare.5104873.v1

CCNC(=O)[C@@H]1CCCN1C(=O)[C@H](C)NC(=O)OCC

Reaction #75324

N-ethoxycarbonyl-L-alanyl-L-proline ethylamide

Rendimiento 47.0%DOI: 10.6084/m9.figshare.5104873.v1

Reaction #75325

N-cyclohexylcarbonyl-L-alanyl-L-proline ethylamide

Rendimiento 60.0%DOI: 10.6084/m9.figshare.5104873.v1

CCNC(=O)[C@@H]1CCCN1C(=O)[C@H](C)NS(=O)(=O)c1ccc(C)cc1

Reaction #75326

N-(p-toluenesulphonyl)-L-alanyl-L-proline ethylamide

Rendimiento 33.0%DOI: 10.6084/m9.figshare.5104873.v1

CCNC(=O)[C@@H]1CCCN1C(=O)[C@H](C)NC(=O)C12CC3CC(CC(C3)C1)C2

Reaction #75327

N-(1-adamantylcarbonyl)-L-alanyl-L-proline ethylamide

Rendimiento 59.0%DOI: 10.6084/m9.figshare.5104873.v1

CCOC(=O)C12CC1C=CCCCCCC(NC(=O)OC(C)(C)C)C(=O)N1CC(Oc3nccc4cc(OC)c(Br)cc34)CC1C(=O)N2

Reaction #247804

DOI: 10.1039/C8SC04228D

$CCOC(=O)[C@@]12C[C@H]1/C=C\CCCCC[C@H](NC(=O)OC(C)(C)C)C(=O)N1C[C@@H](OS(=O)(=O)c3ccc(Br)cc3)C[C@H]1C(=O)N2$

Reaction #325247

title compound

DOI: 10.6084/m9.figshare.5104873.v1

$CCOC(=O)[C@@]12C[C@H]1/C=C\CCCCC[C@H](NC(=O)OC(C)(C)C)C(=O)N1C[C@@H](OS(=O)(=O)c3ccc(Br)cc3)C[C@H]1C(=O)N2$

Reaction #325265

title compound

Rendimiento 87.0%DOI: 10.6084/m9.figshare.5104873.v1

C[N+]1(C)CCC[C@@H](CNC(=O)[C@H]2CCCN2C(=O)[C@@H]2C[C@@H](O)CN2C(=O)CC(c2ccccc2)(c2ccccc2)c2ccccc2)C1.[Br-]

Reaction #359271

title compound

DOI: 10.6084/m9.figshare.5104873.v1

O=C(NC[C@@H]1CCC[N+](CC2CC2)(CC2CC2)C1)[C@H]1CCCN1C(=O)[C@@H]1C[C@@H](O)CN1C(=O)CC(c1ccccc1)(c1ccccc1)c1ccccc1.[Br-]

Reaction #359273

title compound

DOI: 10.6084/m9.figshare.5104873.v1

C=CC[N+]1(CC=C)CCC[C@H](CNC(=O)[C@H]2CCCN2C(=O)[C@@H]2C[C@@H](O)CN2C(=O)CC(c2ccccc2)(c2ccccc2)c2ccccc2)C1.[Br-]

Reaction #359274

title compound

DOI: 10.6084/m9.figshare.5104873.v1

C=CCCCCC[C@H](NC(=O)OC(C)(C)C)C(=O)N1C[C@H](Oc2nccc3cc(OC)c(Br)cc23)C[C@H]1C(=O)N[C@]1(C(=O)OCC)C[C@H]1C=C

Reaction #476399

title product

DOI: 10.6084/m9.figshare.5104873.v1

$CCOC(=O)[C@@]12C[C@H]1/C=C\CCCCC[C@H](NC(=O)OC(C)(C)C)C(=O)N1C[C@H](Oc3nccc4cc(OC)c(Br)cc34)C[C@H]1C(=O)N2$

Reaction #476400

title product

Rendimiento 70.1%DOI: 10.6084/m9.figshare.5104873.v1

$C=CCCC[C@@H]1CCC[C@H]1OC(=O)N[C@H]1CCCCC/C=C\[C@@H]2C[C@@]2(C(=O)OCC)NC(=O)[C@@H]2C[C@H](OS(=O)(=O)c3ccc(Br)cc3)CN2C1=O$

Reaction #476403

Ethyl (2S,6S,12Z,13aS,14aR,16aS)-2-{[(4-bromophenyl)sulfonyl]oxy}-5,16-dioxo-6-[({[(1R,2R)-2-pent-4-en-1-ylcyclopentyl]oxy}carbonyl)amino]-1,2,3,6,7,8,9,10,11,13a,14,15,16,16a-tetradecahydrocyclopropa[e]pyrrolo[1,2-a][1,4]diazacyclopentadecine-14a(5H)-carboxylate

DOI: 10.6084/m9.figshare.5104873.v1

$C=CCCC[C@@H]1CCC[C@H]1OC(=O)N[C@H]1CCCCC/C=C\[C@@H]2C[C@@]2(C(=O)OCC)NC(=O)[C@@H]2C[C@@H](Oc3cc4ccccc4nc3C=C)CN2C1=O$

Reaction #476405

Ethyl (2R,6S,12Z,13aS,14aR,16aS)-5,16-dioxo-6-[({[(1R,2R)-2-pent-4-en-1-ylcyclopentyl]oxy}carbonyl)amino]-2-[(2-vinylquinolin-3-yl)oxy]-1,2,3,6,7,8,9,10,11,13a,14,15,16,16a-tetradecahydrocyclopropa[e]pyrrolo[1,2-a][1,4]diazacyclopentadecine-14a(5H)-carboxylate

DOI: 10.6084/m9.figshare.5104873.v1

Reaction #481222

title compound

DOI: 10.6084/m9.figshare.5104873.v1

Reaction #481223

title compound

DOI: 10.6084/m9.figshare.5104873.v1

CCCC[N+]1(C)CCC[C@H](CNC(=O)[C@H]2CCCN2C(=O)[C@@H]2C[C@@H](O)CN2C(=O)CC(c2ccccc2)(c2ccccc2)c2ccccc2)C1.[Br-]

Reaction #481224

title compound

DOI: 10.6084/m9.figshare.5104873.v1

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