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81.
A stereoselective synthesis of (5S,6S)‐6‐[(2S,5S,7R,8E,10E)‐5‐(benzyloxy)‐7‐{[(tert‐butyl)dimethylsilyl]oxy}‐11‐phenylundeca‐8,10‐dien‐2‐yl]‐5‐ethyl‐5,6‐dihydro‐2H‐pyran‐2‐one (=(+)‐9‐O‐benzyl‐11‐O‐[(tert‐butyl)dimethylsilyl]bitungolide F) is reported. The strategy involves Gilman reaction, olefin cross‐metathesis, and Horner? Wadsworth? Emmons olefination as key steps. 相似文献
82.
Palakodety Radha Krishna Bonepally Karunakar Reddy Palabindela Srinivas 《Tetrahedron》2012,68(3):841-845
Total synthesis of 2-(2-hydroxyalkyl)-piperidine alkaloids, (?)-halosaline and (?)-8-epi-halosaline is reported from n-butyraldehyde using iterative asymmetric allylation, nucleophilic substitution with an azide and ring-closing metathesis as the key reactions. 相似文献
83.
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86.
A rapid, sensitive, and accurate ultra-fast liquid chromatographic method is developed for the determination of related substances and degradants of Solifenacin Succinate, an active pharmaceutical ingredient used in the treatment of overactive bladder. Chromatographic separation of Solifenacin Succinate, its related substances, and degradants was achieved using a Shimpack XR-ODS-II column and mobile phase system containing 10 mM potassium dihydrogen orthophosphate in water. The pH of the buffer was adjusted to 7.0 using triethyl amine (mobile phase A). LC-grade acetonitrile was used as mobile phase B, employing a binary-gradient program at a flow rate 0.5 mL/min. The resolution between the critical pair of peaks (Impurity A and analyte) was found to be greater than 3.5. The limits of detection and quantification (LOQ) of Impurity A, Impurity B, and the analyte were 0.2 and 0.6 μg/mL, respectively for a 5-μL injection volume. The percentage recovery of impurities in the presence of sample matrix ranged from 95 to 104 w/w. The test solution and mobile phase was observed to be stable up to 24 h after the preparation. The validated method yielded good results of precision, linearity, accuracy, robustness, and ruggedness. The proposed method is found to be rapid, accurate, and suitable for the quantitative determination of related substances and degradants during quality control of Solifenacin Succinate active pharmaceutical ingredient. 相似文献
87.
Yan J Garzan A Narayan RS Vasileiou C Borhan B 《Chemistry (Weinheim an der Bergstrasse, Germany)》2010,16(46):13749-13756
In an attempt to revise the structural assignment of mucoxin, and faced with 64 diastereomeric possibilities, we resorted to the synthesis of truncated structures that contained the core stereochemical sites. Twelve stereochemical analogues were synthesized, their (1)H and (13)C NMR spectra were analyzed and four recurring stereochemical trends were distilled from the data. Applying the observed trends to the diastereomeric population pared the possible choices for the correct structure of mucoxin from 64 to 4. Synthesis of these analogues led to the identification of the correct structure of mucoxin. 相似文献
88.
It is well known that if m is an L
p
-multiplier for the Fourier transform on
\mathbbRn{\mathbb{R}^n} , (1 < p < ∞) then there exists a pseudomeasure σ such that T
m
f = σ * f . A similar problem is discussed for the L
p
−Fourier multipliers for H{\mathcal{H}} -valued functions on the Heisenberg group, where H{\mathcal{H}} is a separable Hilbert space. 相似文献
89.
It is well known that if m is an L p -multiplier for the Fourier transform on \({\mathbb{R}^n}\) , (1 < p < ∞) then there exists a pseudomeasure σ such that T m f = σ * f . A similar problem is discussed for the L p ?Fourier multipliers for \({\mathcal{H}}\) -valued functions on the Heisenberg group, where \({\mathcal{H}}\) is a separable Hilbert space. 相似文献
90.
Sequential Baylis-Hillman/ring-closing metathesis (RCM) approach toward the total synthesis of (+)-MK7607 and (+)-streptol starting from (R,R)-tartaric acid is reported. 相似文献