(+)-Rishirilide (4), an inhibitor of α2-macroglobulin, a tetrameric serum glycoprotein that is an irreversible protease inhibitor, has a deceptively simple structure. Thomas R. R. Pettus of the University of California…
Albert Padwa of Emory University has developed (Org. PMID:23664186 Fmoc-Ala-OH supplier Lett. 2006, 8, 3275. DOI: 10.1021/ol061137i) a productive approach to fused indole alkaloids such as aspidophytine (3), based on…
The total synthesis of steroids such as (+)-digitoxigenin (3) has been studied for more than sixty years, yet it has never been thought that such studies would lead to a…
The report last year by scientists at Merck of an antibiotic, platensimycin3, with a novel mechanism of action has led to much effort toward the total synthesis of this degraded…
Historically, there have been three methods for assembling enantiomerically-pure carbocycles: cyclization of an enantiomerically-pure starting material, enantioselective cyclization of a prochiral substrate, and enantioselective transformation of a prochiral cyclic starting…
Jin-Quan Yu of Cambridge University reports (Org. PMID:35567400 Lett. 2003, 5, 4665. DOI: 10.1021/ol0358509) that Pd nanoparticles catalyze the hydrogenolysis of benzylic epoxides. The reaction proceeds with inversion of absolute…
Sharpless asymmetric epoxidation has long been a workhorse of enantioselective synthesis. The SAE protocol, however, gives only mediocre ee’s with cis allylic alcohols such as nerol (1). PMID:23381626 Hisashi Yamamoto…
Green or sustainable chemistry has now attained the status of a major scientific discipline (Green Chemistry: Theory and Practice, 1998, Oxford Press) and the studies in this area have led…
Alcohols are the most common functional group protected, and benzyl is the most commonly used alcohol protecting group. Gregory B. Dudley of Florida State University has developed (J. Org. Chem.…
The aza-Baylis-Hillman (aza-BH) reaction is a nucleophile-catalysed coupling of an imine with an electron-deficient olefin which provides direct access to highly functionalized chiral amines from readily available achiral starting materials.…
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