An enantioselective synthesis of (−)-4-hydroxy-6-methoxy-3a,8a-dihydrofuro[2,3-b]benzofuran: an advanced intermediate in the synthesis of (−)-aflatoxin B1 and G1
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference28 articles.
1. Preparation of the 8,9-epoxide of the mycotoxin aflatoxin B1: the ultimate carcinogenic species
2. Preparation and characterization of an aflatoxin B1 adduct with the oligodeoxynucleotide d(ATCGAT)2
3. Intercalation of aflatoxin B1 in two oligodeoxynucleotide adducts: comparative proton NMR analysis of d(ATCAFBGAT).cntdot.d(ATCGAT) and d(ATAFBGCAT)2
4. Total synthesis of racemic aflatoxin B1
5. Total syntheses of aflatoxins M1 and G1 and an improved synthesis of aflatoxin B1
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3. Direct Access to 3-Thioether-Substituted Dihydrofuro[2,3-b]benzofurans via Tandem Reactions of Sulfur Ylides and 2-Nitrobenzofurans;The Journal of Organic Chemistry;2023-07-18
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