Stereoselective Total Syntheses of (+)-Castanospermine and Neu5Ac Methyl Ester
Author:
Affiliation:
1. School of Pharmacy, Sungkyunkwan University, Seobu-ro 2066, Suwon-si, Gyeonggi-do 16419, Republic of Korea
2. Yonsung Fine Chemicals Co., Ltd., Sujeong-ro 207, Jangan-myeon, Hwaseong-si, Gyeonggi-do 18581, Republic of Korea
Funder
Yonsung Fine Chemicals Co., Ltd.
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.9b00216
Reference68 articles.
1. Asymmetric total syntheses of (+)-2,5-dideoxy-2,5-imino-d-glucitol [(+)-DGDP] and (−)-1-deoxymannojirimycin [(−)-DMJ] via an extended chiral 1,3-oxazine
2. Asymmetric total synthesis of (−)-conduramine A-1 via a chiral syn , anti -oxazine
3. Stereoselective Chirality Extension of syn,anti- and syn,syn-Oxazine and Stereochemical Analysis of Chiral 1,3-Oxazines: Stereoselective Total Syntheses of (+)-1-Deoxygalactonojirimycin and (−)-1-Deoxygulonojirimycin
4. Stereoselective total synthesis of (+)-radicamine B via anti,syn,syn -oxazine
5. 1,3-Oxazine as a chiral building block used in the total synthesis of (+)-1-deoxynojirimycin and (2R,5R)-dihydroxymethyl-(3R,4R)-dihydroxypyrrolidine
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