(S)-2-(Toluene-4-sulfonylamino)-6-((2R,3S,4R)-3,4,5-trihydroxy-tetrahydro-furan-2-yl)-hexanoic acid benzyl ester

Base Information

Chemical Name:(S)-2-(Toluene-4-sulfonylamino)-6-((2R,3S,4R)-3,4,5-trihydroxy-tetrahydro-furan-2-yl)-hexanoic acid benzyl ester
CAS No.:1059579-93-9
Molecular Formula:C₂₄H₃₁NO₈S
Molecular Weight:493.578
Hs Code.:

Synonyms:(S)-2-(Toluene-4-sulfonylamino)-6-((2R,3S,4R)-3,4,5-trihydroxy-tetrahydro-furan-2-yl)-hexanoic acid benzyl ester

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Chemical Property of (S)-2-(Toluene-4-sulfonylamino)-6-((2R,3S,4R)-3,4,5-trihydroxy-tetrahydro-furan-2-yl)-hexanoic acid benzyl ester

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Technology Process of (S)-2-(Toluene-4-sulfonylamino)-6-((2R,3S,4R)-3,4,5-trihydroxy-tetrahydro-furan-2-yl)-hexanoic acid benzyl ester

There total 10 articles about (S)-2-(Toluene-4-sulfonylamino)-6-((2R,3S,4R)-3,4,5-trihydroxy-tetrahydro-furan-2-yl)-hexanoic acid benzyl ester 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:

: 160451-23-0
Benzyl -β-D-ribo-decofuranosid>uronate

: 1059579-93-9
(S)-2-(Toluene-4-sulfonylamino)-6-((2R,3S,4R)-3,4,5-trihydroxy-tetrahydro-furan-2-yl)-hexanoic acid benzyl ester

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; at 22 ℃; for 44h; Yield given;
DOI:10.1021/jo00094a033

Reference yield:

: 33985-40-9
(3aR,4S,6R,6aR)-tetrahydro-6-methoxy-2,2-dimethylfuro-[3,4-d][1,3]dioxole-4-carbaldehyde

: 1059579-93-9
(S)-2-(Toluene-4-sulfonylamino)-6-((2R,3S,4R)-3,4,5-trihydroxy-tetrahydro-furan-2-yl)-hexanoic acid benzyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: F(-)

2: dehydratation

3: reduction

4: ceric ammonium nitrate

5: 94 percent / oxalic acid / ethanol / 24 h / 22 °C

6: 50 percent / catecholborane / tetrahydrofuran; CHCl₃ / 24 h / 0 °C

7: 4 M aq. HCl / dioxane / 44 h / 22 °C

With hydrogenchloride; ammonium cerium(IV) nitrate; oxalic acid; benzo[1,3,2]dioxaborole; fluoride; In tetrahydrofuran; 1,4-dioxane; ethanol; chloroform;
DOI:10.1021/jo00094a033

Reference yield:

: 2978-10-1
O-benzyl-N,N'-diisopropylisourea

: 1059579-93-9
(S)-2-(Toluene-4-sulfonylamino)-6-((2R,3S,4R)-3,4,5-trihydroxy-tetrahydro-furan-2-yl)-hexanoic acid benzyl ester

Guidance literature:: Multi-step reaction with 8 steps

2: F(-)

3: dehydratation

4: reduction

5: ceric ammonium nitrate

6: 94 percent / oxalic acid / ethanol / 24 h / 22 °C

7: 50 percent / catecholborane / tetrahydrofuran; CHCl₃ / 24 h / 0 °C

8: 4 M aq. HCl / dioxane / 44 h / 22 °C

With hydrogenchloride; ammonium cerium(IV) nitrate; oxalic acid; benzo[1,3,2]dioxaborole; fluoride; In tetrahydrofuran; 1,4-dioxane; ethanol; chloroform;
DOI:10.1021/jo00094a033