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HCID 13236168, compound → HCID 178468711, compound

HRID 1490716
Notes
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Reaction equation

HRID 1490716 reaction equation
CCOC(=O)c1ccccc1Cc1ccccc1>C1=CCCC=CCC1.C1=CCCC=CCC1.C1CCOC1.CC(C)(C)O.CC1(C)OB(B2OC(C)(C)C(C)(C)O2)OC1(C)C.C[OH2+].C[OH2+].O=c1ccc2cccc(-c3ccc(-c4ccccn4)nc3)c2[nH]1.[Ir].[Ir].[K]>CCOC(=O)c1ccc(B2OC(C)(C)C(C)(C)O2)cc1Cc1ccccc1
ParticipantsConditionsSources & evidenceReaction notes

Participants

7

Reactant 1

HCID 13236168HCID 13236168, compound

Product 1

HCID 178468711HCID 178468711, compoundYield 87%

Reagents, catalysts & solvents 5

HCID 2733548Bis(pinacolato)diboraneReagentHCID 86639980Potassium tert-butoxideReagentHCID 1646813858-([2,2'-bipyridin]-5-yl)quinolin-2(1H)-oneReagentHCID 76001521Bis(1,5-cyclooctadiene)dimethoxydiiridiumCatalystHCID 8028TetrahydrofuranSolvent

Conditions

Temperature
80 °C

Sources & evidence

ORD record
ord-52c79f3fd2d643f78e41e9aba3acb70d
Source dataset
Borylation dataset from Roche
DOI
10.1021/jacs.7b04490

Reaction notes

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On this pageParticipantsConditionsSources & evidenceReaction notes