tert-butyl (1S,2R)-1-((S)-1,2-dideuterocyclohex-2-enyl)-3-oxo-1-(tetrahydro-2H-pyran-2-yloxy)propan-2-ylcarbamate

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Chemical Name:tert-butyl (1S,2R)-1-((S)-1,2-dideuterocyclohex-2-enyl)-3-oxo-1-(tetrahydro-2H-pyran-2-yloxy)propan-2-ylcarbamate
CAS No.:1309572-13-1
Molecular Formula:C₁₉H₃₁NO₅
Molecular Weight:355.443
Hs Code.:

Synonyms:

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Chemical Property of tert-butyl (1S,2R)-1-((S)-1,2-dideuterocyclohex-2-enyl)-3-oxo-1-(tetrahydro-2H-pyran-2-yloxy)propan-2-ylcarbamate

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Technology Process of tert-butyl (1S,2R)-1-((S)-1,2-dideuterocyclohex-2-enyl)-3-oxo-1-(tetrahydro-2H-pyran-2-yloxy)propan-2-ylcarbamate

There total 9 articles about tert-butyl (1S,2R)-1-((S)-1,2-dideuterocyclohex-2-enyl)-3-oxo-1-(tetrahydro-2H-pyran-2-yloxy)propan-2-ylcarbamate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: C₂₆H₃₅NO₅

: 1309572-13-1
tert-butyl (1S,2R)-1-((S)-1,2-dideuterocyclohex-2-enyl)-3-oxo-1-(tetrahydro-2H-pyran-2-yloxy)propan-2-ylcarbamate

Guidance literature:: Multi-step reaction with 6 steps

1.1: diisobutylaluminium hydride / hexane; toluene / 2 h / -78 °C / Inert atmosphere

1.2: -78 - 20 °C

2.1: chromium dichloride; sodium iodide / tetrahydrofuran / 20 °C / Inert atmosphere

3.1: Grubbs catalyst first generation / dichloromethane / 20 °C / Inert atmosphere

4.1: pyridinium p-toluenesulfonate / dichloromethane / Inert atmosphere

5.1: tetrabutyl ammonium fluoride / tetrahydrofuran

6.1: Dess-Martin periodane / dichloromethane

With Grubbs catalyst first generation; chromium dichloride; tetrabutyl ammonium fluoride; pyridinium p-toluenesulfonate; diisobutylaluminium hydride; Dess-Martin periodane; sodium iodide; In tetrahydrofuran; hexane; dichloromethane; toluene; 2.1: Nozaki-Hiyama-Kishi reaction;
DOI:10.1021/ol201120k

Reference yield:

: C₂₅H₃₃NO₄

: 1309572-13-1
tert-butyl (1S,2R)-1-((S)-1,2-dideuterocyclohex-2-enyl)-3-oxo-1-(tetrahydro-2H-pyran-2-yloxy)propan-2-ylcarbamate

Guidance literature:: Multi-step reaction with 5 steps

1: chromium dichloride; sodium iodide / tetrahydrofuran / 20 °C / Inert atmosphere

2: Grubbs catalyst first generation / dichloromethane / 20 °C / Inert atmosphere

3: pyridinium p-toluenesulfonate / dichloromethane / Inert atmosphere

4: tetrabutyl ammonium fluoride / tetrahydrofuran

5: Dess-Martin periodane / dichloromethane

With Grubbs catalyst first generation; chromium dichloride; tetrabutyl ammonium fluoride; pyridinium p-toluenesulfonate; Dess-Martin periodane; sodium iodide; In tetrahydrofuran; dichloromethane; 1: Nozaki-Hiyama-Kishi reaction;
DOI:10.1021/ol201120k

Reference yield:

: (E)-2,3-dideuteroocta-2,7-dien-1-ol

: 1309572-13-1
tert-butyl (1S,2R)-1-((S)-1,2-dideuterocyclohex-2-enyl)-3-oxo-1-(tetrahydro-2H-pyran-2-yloxy)propan-2-ylcarbamate

Guidance literature:: Multi-step reaction with 6 steps

1: pyridine; dmap / dichloromethane / 0 - 20 °C / Inert atmosphere

2: chromium dichloride; sodium iodide / tetrahydrofuran / 20 °C / Inert atmosphere

3: Grubbs catalyst first generation / dichloromethane / 20 °C / Inert atmosphere

4: pyridinium p-toluenesulfonate / dichloromethane / Inert atmosphere

5: tetrabutyl ammonium fluoride / tetrahydrofuran

6: Dess-Martin periodane / dichloromethane

With pyridine; Grubbs catalyst first generation; chromium dichloride; dmap; tetrabutyl ammonium fluoride; pyridinium p-toluenesulfonate; Dess-Martin periodane; sodium iodide; In tetrahydrofuran; dichloromethane; 2: Nozaki-Hiyama-Kishi reaction;
DOI:10.1021/ol201120k