(1R)-10-phenylsulfonylisobornyl (Z)-3-[(1S)-1-methoxycarbonylethylamino]but-2-enoate

Base Information

Chemical Name:(1R)-10-phenylsulfonylisobornyl (Z)-3-[(1S)-1-methoxycarbonylethylamino]but-2-enoate
CAS No.:1198579-41-7
Molecular Formula:C₂₄H₃₃NO₆S
Molecular Weight:463.595
Hs Code.:

Synonyms:(1R)-10-phenylsulfonylisobornyl (Z)-3-[(1S)-1-methoxycarbonylethylamino]but-2-enoate

Suppliers and Price of (1R)-10-phenylsulfonylisobornyl (Z)-3-[(1S)-1-methoxycarbonylethylamino]but-2-enoate

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (1R)-10-phenylsulfonylisobornyl (Z)-3-[(1S)-1-methoxycarbonylethylamino]but-2-enoate

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Technology Process of (1R)-10-phenylsulfonylisobornyl (Z)-3-[(1S)-1-methoxycarbonylethylamino]but-2-enoate

There total 1 articles about (1R)-10-phenylsulfonylisobornyl (Z)-3-[(1S)-1-methoxycarbonylethylamino]but-2-enoate 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: 69.0%

: 2491-20-5
L-alanine methyl ester hydrochloride

: 607732-31-0
(1R)-(+)-10-(phenylsulfonyl)isobornyl buta-2,3-dienoate

: 1198579-41-7
(1R)-10-phenylsulfonylisobornyl (Z)-3-[(1S)-1-methoxycarbonylethylamino]but-2-enoate

Guidance literature:: With sodium hydrogencarbonate; In methanol; at 20 ℃;
DOI:10.1016/j.tet.2009.09.041

Reference yield: 88.0%

: 1198579-41-7
(1R)-10-phenylsulfonylisobornyl (Z)-3-[(1S)-1-methoxycarbonylethylamino]but-2-enoate

: 1198579-43-9
(1R)-10-phenylsulfonylisobornyl (S)-3-[(1S)-1-methoxycarbonylethylamino]butanoate

Guidance literature:: With sodium tetrahydroborate; acetic acid; In acetonitrile; at 0 ℃; for 4h; diastereoselective reaction;
DOI:10.1016/j.tet.2009.09.041