N-δ-Carbobenzoxy-N-δ-methyl-δ-aminovaleric acid t-butyl ester
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N-δ-Carbobenzoxy-N-δ-methyl-δ-aminovaleric acid t-butyl ester

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Category
CBZ-Amino Acids
Catalog number
BAT-001437
Molecular Formula
C18H27NO4
Molecular Weight
321.42
Synonyms
N-delta-Carbobenzoxy-N-delta-methyl-delta-aminovaleric acid t-butyl ester; Z-MeApe(5)-OtBu; 5-[Carbobenzoxy(methyl)amino]pentanoic acid t-butyl ester
1. General anesthetics and β-amyloid protein
Zhongcong Xie, Zhipeng Xu Prog Neuropsychopharmacol Biol Psychiatry. 2013 Dec 2;47:140-6. doi: 10.1016/j.pnpbp.2012.08.002. Epub 2012 Aug 14.
With roughly 234 million people undergoing surgery with anesthesia each year worldwide, it is important to determine whether commonly used anesthetics can induce any neurotoxicity. Alzheimer's disease (AD) is the most common form of age-related dementia, and a rapidly growing health problem. Several studies suggest that anesthesia could be associated with the development of AD. Moreover, studies in cultured cells and animals show that commonly used inhalation anesthetics may induce changes consistent with AD neuropathogenesis, e.g., β-amyloid protein accumulation. Therefore, in this mini review, we focus on the recent research investigating the effects of commonly used anesthetics including isoflurane, sevoflurane, desflurane, nitrous oxide, and propofol, on Aβ accumulation in vitro and in vivo. We further discuss the future direction of the research determining the effects of anesthetics on β-amyloid protein accumulation.
2. Total Synthesis of (+)-Trachyspic Acid 19- n- Butyl Ester
Alex A Rafaniello, Mark A Rizzacasa Org Lett. 2020 Mar 6;22(5):1972-1975. doi: 10.1021/acs.orglett.0c00319. Epub 2020 Feb 17.
The first total synthesis of the alkyl citrate trachyspic acid 19-n-butyl ester (1) is described. A formal [2 + 2]-cycloaddition of the silylketene acetal derived from lactone 6 with di-n-butylacetylene dicarboxylate 7 provided the cyclobutene diester 5 with a dr >20:1. Acid-mediated rearrangement of 5 followed by lactone ring-opening and ester protecting group manipulation eventually provided orthogonally protected aldehyde 3. A Nozaki-Hiyama-Kishi coupling between 3 and vinyl iodide 4 followed by oxidation of the resultant allylic alcohol gave enone 16, which was converted into the triester 17 (dr 6:1) by a spirocyclization/oxidative cleavage/elimination sequence. Removal of the t-butyl esters then afforded trachyspic acid 19-n-butyl ester (1).
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