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11.
Zlatopolskiy BD Loscha K Alvermann P Kozhushkov SI Nikolaev SV Zeeck A de Meijere A 《Chemistry (Weinheim an der Bergstrasse, Germany)》2004,10(19):4708-4717
The complete absolute configuration of hormaomycin 1 a has been established by HPLC and HPLC/MS experiments with appropriately derivatized 4-propylprolines, (2S,4S)-6 and (2R,4R)-6, as well as 4-(Z)-propenylprolines, cis-5 and trans-5, and also feeding experiments with enantiomerically pure samples of the deuterium-labeled 3-(2'-nitrocyclopropyl)alanine, (2S)-3,3-[D2]15 and (2S)-2,2'-[D2]15, and 4-(Z)-propenylproline 2',4-[D2]-(2S,4R)-5. The latter five amino acids were prepared for the first time and allowed one to unequivocally assign the hitherto unknown absolute configurations of the last four stereocenters in hormaomycin 1 a. As a bonus, some new information about the biosynthesis of this molecule has also been gathered. 相似文献
12.
H. Etori H. Hirata Y. Yamada H. Okabayashi M. Furusaka 《Colloid and polymer science》1997,275(3):263-273
Potassium salts of N-decanoylglycine and N-decanoyl-L-alanine oligopeptides (monomer, dimer and trimer) were synthesized.
For these oligomer salts in aqueous solutions, the microstructures of micelles have been investigated by small-angle neutron-scattering
(SANS). In the calculation of SANS intensity data, the thickness of the hydrophilic layer was altered by changing the conformation
of the oligomer moiety (helical and β-sheet structures). For micelles of the trimer salts, the helical structure models provide
the best fit to the observed SANS intensity data. For micelles of the monomer-and dimer-salts, the β-sheet model provides
the best fit to the observed data. For the monomer-and dimer-micelles, the aggregation number (n) is not dependent on the species of amino acid residue, imply-ing that the decanoyl group plays a critical role in micelle
formation. However, for the trimer micelles, the n value is dependent on the species of amino acid residue.
Received: 11 July 1996 Accepted: 11 September 1996 相似文献
13.
The sequential treatment of various tertiary N-methyl and N-benzylamines with carbon disulfide, and then with an alkyl halide in tetrahydrofuran gave the corresponding dithiocarbamates in good to excellent yields. 相似文献
14.
Jing Zhou Shihua Song Feng Jiang Chunling Fu Prof. Shengming Ma 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(42):9948-9958
Herein, we report the total synthesis of traumatic lactone and rhizobialide by utilizing allenoic acid to construct the lactone ring. The key starting materials, allenoic acids, could be prepared by the ATA (allenation of terminal alkynes) of a terminal alkyne with an aldehyde that contained a protected hydroxyl group followed by hydrolysis. Importantly, the asymmetric synthesis could be realized just by replacing racemic diphenylprinol with (R)- or (S)-diphenylprinol to deliver the optically active allenoate. 相似文献
15.
One new sesquiterpene lactone,1 α,8 α,9 α-trihydroxyeudesman-3(4),7(11)-dien-8 β,12-olide(1) and two new phenylpropanoidsubstituted catechin glycosides,glabraoside C(2) and glabraoside D(3) were isolated from the whole plant of Sarcandra glabra. Their structures were established by the analyses of spectral and chemical evidences. 相似文献
16.
Zheng Li Jin-Lan Yu Sheng-Yi Shi Wei Zhu 《Phosphorus, sulfur, and silicon and the related elements》2013,188(5):1031-1037
A rapid method to N-acyl ureas from corresponding N-acyl thioureas is described. N-coumaroyl-N′-arylthioureas, which are easily prepared by the reaction of coumarin-3-carboxylic acid chloride with potassium thiocyanate and arylamines, can be expeditiously transformed into corresponding N-acyl ureas via r.t. grinding with wet silica supported potassium permanganate under solvent-free conditions in an excellent yield. 相似文献
17.
Stereoselective total synthesis of two chiral lactones, (+)‐trans‐cognac lactone (1b) and (+)‐trans‐aerangis lactone (2c), has been achieved from the same intermediate using a radical‐based cyclization route. 相似文献
18.
Chadi Khoury François Le Goffic Marie‐Noëlle Rager 《Journal of carbohydrate chemistry》2013,32(7):395-409
The synthesis of 2‐acetamido‐2‐deoxy‐6‐O‐octanoyl‐D‐glucono‐1,5‐lactone 9 and 2‐acetamido‐2‐deoxy‐6‐O‐octanoyl‐α‐D‐glucopyranose 7 from 2‐acetamido‐2‐deoxy‐α‐D‐glucopyranose is reported. For both targets, the key intermediate was allyl 2‐acetamido‐3,4‐di‐O‐benzyl‐2‐deoxy‐6‐O‐octanoyl‐α‐D‐glucopyranoside 5. Surface tension measurements (critical micellar concentration of 22.3 mM and 5 mM for 9 and 7, respectively) showed up the surface activity of both compounds, while enzyme inhibition assays indicated that 9 could inhibit bovine β‐N‐acetylglucosaminidase (Ki=6.5 µM) but not Serratia marcescens chitobiase nor hen egg‐white lysozyme. Moreover, 7 was shown to induce chitinase production of S. marcescens and to be readily metabolized by these bacteria. 相似文献
19.
Triflic acid-mediated stereoselective direct lactonization of a variety of α-amino γ,δ-unsaturated carboxylic acid esters and the construction of new γ-butyrolactone structural motifs are reported. Several α-amino γ,δ-unsaturated carboxylic acid esters underwent stereo- and regioselective 1,5-cyclization and afforded a variety of highly substituted homoserine lactone scaffolds having contiguous stereocenters. The direct lactonization of the chiral α-amino γ,δ-unsaturated carboxylic acid esters with triflic acid led to the enantioselective synthesis of the novel homoserine lactones. A plausible mechanism for the direct lactonization of α-amino γ,δ-unsaturated carboxylic acid esters is presented. The stereochemistry of major isomers 3f, 7a, 7b, and 7d was unambiguously established from the X-ray structure analysis. 相似文献
20.
An enantiospecific total synthesis of polyhydroxy δ-pyrone natural product (+)-anamarine is accomplished. The main features of the synthesis include the stereoselective reduction of the ketone obtained by the desymmetrization of the bis-dimethyl amide of tartaric acid and further elaboration involving asymmetric Brown's allylation and ring closing metathesis. 相似文献