(4aR,5Z,E)-5-O-Benzyl-4a-carba-4a-hydroxy-2,3-O-isopropylidene-1-O-triisopropylsilyl-β-D-erythro-pent-4-enofuranose

Base Information

Chemical Name:(4aR,5Z,E)-5-O-Benzyl-4a-carba-4a-hydroxy-2,3-O-isopropylidene-1-O-triisopropylsilyl-β-D-erythro-pent-4-enofuranose
CAS No.:243462-58-0
Molecular Formula:C₂₅H₄₀O₅Si
Molecular Weight:448.675
Hs Code.:

Synonyms:(4aR,5Z,E)-5-O-Benzyl-4a-carba-4a-hydroxy-2,3-O-isopropylidene-1-O-triisopropylsilyl-β-D-erythro-pent-4-enofuranose

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Chemical Property of (4aR,5Z,E)-5-O-Benzyl-4a-carba-4a-hydroxy-2,3-O-isopropylidene-1-O-triisopropylsilyl-β-D-erythro-pent-4-enofuranose

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Technology Process of (4aR,5Z,E)-5-O-Benzyl-4a-carba-4a-hydroxy-2,3-O-isopropylidene-1-O-triisopropylsilyl-β-D-erythro-pent-4-enofuranose

There total 1 articles about (4aR,5Z,E)-5-O-Benzyl-4a-carba-4a-hydroxy-2,3-O-isopropylidene-1-O-triisopropylsilyl-β-D-erythro-pent-4-enofuranose 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: 60.0%

: 243462-53-5
(4aS)-4,4a-Anhydro-5-O-benzyl-4a-carba-1-O-(triisopropylsilyl)-2,3-O-isopropylidene-β-L-lyxofuranose

: 243462-58-0
(4aR,5Z,E)-5-O-Benzyl-4a-carba-4a-hydroxy-2,3-O-isopropylidene-1-O-triisopropylsilyl-β-D-erythro-pent-4-enofuranose

Guidance literature:: With lithium diethylamide; In diethyl ether; hexane; at -10 - 20 ℃; for 6h;
DOI:10.1515/znb-1999-0817

Reference yield: 76.0%

: 243462-58-0
(4aR,5Z,E)-5-O-Benzyl-4a-carba-4a-hydroxy-2,3-O-isopropylidene-1-O-triisopropylsilyl-β-D-erythro-pent-4-enofuranose

: 243462-59-1
(4aR)-5-O-Benzyl-4a-carba-2,3-O-isopropylidene-1-O-triisopropylsilyl-4a-hydroxy-β-L-lyxofuranose

Guidance literature:: With hydrogen; palladium on activated charcoal; In tetrahydrofuran; for 4h;
DOI:10.1515/znb-1999-0817

Reference yield:

: 243462-58-0
(4aR,5Z,E)-5-O-Benzyl-4a-carba-4a-hydroxy-2,3-O-isopropylidene-1-O-triisopropylsilyl-β-D-erythro-pent-4-enofuranose

: (4aR)-5-O-Benzyl-4a-carba-2,3-O-isopropylidene-1-O-triisopropylsilyl-4a-O-(3,5-dinitrobenzoyl)-β-L-lyxofuranose

Guidance literature:: Multi-step reaction with 2 steps

1: 76 percent / H₂ / 5 percent Pd/C / tetrahydrofuran / 4 h

2: 99 percent / pyridine / 6 h / 25 °C

With pyridine; hydrogen; palladium on activated charcoal; In tetrahydrofuran; 1: Catalytic hydrogenation / 2: Esterification;
DOI:10.1515/znb-1999-0817