(1S,4R)-4-[((3aR,5S,6R,6aR)-2,2-Dimethyl-5-trityloxymethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl)-hydroxy-amino]-cyclohex-2-enol

Base Information

Chemical Name:(1S,4R)-4-[((3aR,5S,6R,6aR)-2,2-Dimethyl-5-trityloxymethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl)-hydroxy-amino]-cyclohex-2-enol
CAS No.:143417-01-0
Molecular Formula:C₃₃H₃₇NO₆
Molecular Weight:543.66
Hs Code.:

Synonyms:(1S,4R)-4-[((3aR,5S,6R,6aR)-2,2-Dimethyl-5-trityloxymethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl)-hydroxy-amino]-cyclohex-2-enol

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Chemical Property of (1S,4R)-4-[((3aR,5S,6R,6aR)-2,2-Dimethyl-5-trityloxymethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl)-hydroxy-amino]-cyclohex-2-enol

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Technology Process of (1S,4R)-4-[((3aR,5S,6R,6aR)-2,2-Dimethyl-5-trityloxymethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl)-hydroxy-amino]-cyclohex-2-enol

There total 3 articles about (1S,4R)-4-[((3aR,5S,6R,6aR)-2,2-Dimethyl-5-trityloxymethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl)-hydroxy-amino]-cyclohex-2-enol 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: 76.0%

: 143416-98-2
C₃₃H₃₅NO₆

: 143417-01-0
(1S,4R)-4-[((3aR,5S,6R,6aR)-2,2-Dimethyl-5-trityloxymethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl)-hydroxy-amino]-cyclohex-2-enol

Guidance literature:: With hydrogenchloride; sodium cyanoborohydride; In methanol;

Reference yield:

: 143416-86-8
(3aR,5S,6R,6aR)-2,2-Dimethyl-6-nitroso-5-trityloxymethyl-tetrahydro-furo[2,3-d][1,3]dioxole

: 143417-01-0
(1S,4R)-4-[((3aR,5S,6R,6aR)-2,2-Dimethyl-5-trityloxymethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl)-hydroxy-amino]-cyclohex-2-enol

Guidance literature:: Multi-step reaction with 3 steps

1: 72 percent / CHCl₃ / 2 h / Heating

2: 39 percent / m-chloroperbenzoic acid / CHCl₃ / 1.5 h / Ambient temperature

3: 76 percent / NaBH₃CN, aq. HCl / methanol

With hydrogenchloride; sodium cyanoborohydride; 3-chloro-benzenecarboperoxoic acid; In methanol; chloroform;

Reference yield:

: 143416-92-6
(1S,4R)-3-((3aR,5S,6R,6aR)-2,2-Dimethyl-5-trityloxymethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl)-2-oxa-3-aza-bicyclo[2.2.2]oct-5-ene

: 143417-01-0
(1S,4R)-4-[((3aR,5S,6R,6aR)-2,2-Dimethyl-5-trityloxymethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl)-hydroxy-amino]-cyclohex-2-enol

Guidance literature:: Multi-step reaction with 2 steps

1: 39 percent / m-chloroperbenzoic acid / CHCl₃ / 1.5 h / Ambient temperature

2: 76 percent / NaBH₃CN, aq. HCl / methanol

With hydrogenchloride; sodium cyanoborohydride; 3-chloro-benzenecarboperoxoic acid; In methanol; chloroform;