tert-butyl (3S,4R,5S,6R)-3-(N-isopropyl-N-benzylamino)-4,5,6,7-tetrahydroxy-4,5,6,7-di-O-isopropylideneheptanoate

Base Information

Chemical Name:tert-butyl (3S,4R,5S,6R)-3-(N-isopropyl-N-benzylamino)-4,5,6,7-tetrahydroxy-4,5,6,7-di-O-isopropylideneheptanoate
CAS No.:1454884-13-9
Molecular Formula:C₂₇H₄₃NO₆
Molecular Weight:477.642
Hs Code.:

Synonyms:tert-butyl (3S,4R,5S,6R)-3-(N-isopropyl-N-benzylamino)-4,5,6,7-tetrahydroxy-4,5,6,7-di-O-isopropylideneheptanoate

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Chemical Property of tert-butyl (3S,4R,5S,6R)-3-(N-isopropyl-N-benzylamino)-4,5,6,7-tetrahydroxy-4,5,6,7-di-O-isopropylideneheptanoate

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Technology Process of tert-butyl (3S,4R,5S,6R)-3-(N-isopropyl-N-benzylamino)-4,5,6,7-tetrahydroxy-4,5,6,7-di-O-isopropylideneheptanoate

There total 1 articles about tert-butyl (3S,4R,5S,6R)-3-(N-isopropyl-N-benzylamino)-4,5,6,7-tetrahydroxy-4,5,6,7-di-O-isopropylideneheptanoate 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:

: 1454884-08-2
tert-butyl (4R,5S,6R,E)-4,5,6,7-tetrahydroxy-4,5,6,7-di-O-isopropylidenehept-2-enoate

: 102-97-6
Benzyl-isopropyl-amin

: 1454884-13-9
tert-butyl (3S,4R,5S,6R)-3-(N-isopropyl-N-benzylamino)-4,5,6,7-tetrahydroxy-4,5,6,7-di-O-isopropylideneheptanoate

: 1454884-12-8
tert-butyl (3S,4R,5S,6R)-3-(N-isopropyl-N-benzylamino)-4,5,6,7-tetrahydroxy-4,5,6,7-di-O-isopropylideneheptanoate

Guidance literature:: Benzyl-isopropyl-amin; With n-butyllithium; In tetrahydrofuran; hexane; at -78 ℃; for 0.5h; Inert atmosphere;

tert-butyl (4R,5S,6R,E)-4,5,6,7-tetrahydroxy-4,5,6,7-di-O-isopropylidenehept-2-enoate; In tetrahydrofuran; hexane; at -78 ℃; for 2h; Overall yield = 85 %; Overall yield = 1.86 g; diastereoselective reaction; Inert atmosphere;
DOI:10.1016/j.tet.2013.07.096