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101.
Symbiodinolide is a polyol macrolide isolated from the marine dinoflagellate Symbiodinium sp. in 2007. The C14-C24 fragment of symbiodinolide possessing the 17R/18R/21R absolute configuration, which was obtained as one of the degraded products of symbiodinolide, was synthesized stereoselectively from cis-2-butene-1,4-diol. The detailed comparison of the synthetic product with the degraded product in the spectroscopic data confirmed that the stereostructure of the C14-C24 fragment was 17R, 18R, and 21R. 相似文献
102.
Chunguang HanYoshi Yamano Fumitoshi KakiuchiKazuhiko Nakamura Daisuke Uemura 《Tetrahedron》2011,67(49):9622-9626
An oxidative cleavage of allyl vic-diols to aldehydes catalyzed by a Grubbs carbene complex using a co-oxidant has been established for the first time, with good yields. The utility of this selective cleavage reaction was demonstrated through the use of two huge marine molecules, symbiodinolide and N-p-BrBz palytoxin. 相似文献
103.
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105.
Masahiro Yamashita Daisuke Kawakami Satoshi Matsunaga Yoshio Nakayama Mari Sasaki Shinya Takaishi Fumiyasu Iwahori Hitoshi Miyasaka Ken‐ichi Sugiura Yoshiki Wada Hiroshi Miyamae Hiroyuki Matsuzaki Hiroshi Okamoto Hisaaki Tanaka Kazuhiro Marumoto Shin‐ichi Kuroda 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2004,116(36):4867-4871
106.
We discuss a rigid string model proposed by Casalbuoni and Longhi. Constraints for the massive states are solved to find the physical states and the mass spectrum. We also find its supersymmetric extension with the kappa symmetry. The supersymmetry transformations are found starting from on-shell transformations using the Dirac bracket. 相似文献
107.
[structure: see text] 8,11-Dideoxytetrodotoxin, an unnatural tetrodotoxin analogue, was synthesized in a highly stereoselective manner from a common intermediate in our synthetic studies on tetrodotoxin. The synthesis features neighboring group participation of trichloroacetamide for stereoselective hydroxylation, protection of ortho ester, and guanidine installation with Boc-protected isothiourea. 相似文献
108.
109.
Yuji Hayashi Takeshi Matsumoto Motokazu Uemura Masato Koreeda 《Magnetic resonance in chemistry : MRC》1980,14(2):86-91
Carbon-13 NMR signals of the biologically active norditerpenoid dilactones from Podocarpus plants were fully assigned by using selective 1H decoupling, coupling constants (2JCH), spin-lattice relaxation times (T1) and correlation of the spectra of more than thirty dilactone congeners. The spectra of five nagilactones, B, C, D, E and F, which constitute representative members of three major structural types of the dilactones: (A) 8:14, 9:11-dienolide (α-pyrone) type, (B) 7α:8α-epoxy-9:11-enolide type, and (C) 7:8,9:11-dienolide type, were extensively analysed. Some characteristic steric interactions for the substituents on the ring system can be demonstrated from the spectral properties. 相似文献
110.
The diffusion constant (D) and the spin depolarisation rate (λS) of the positive muon in the ferromagnetic b.c.c. lattices such as Fe have been calculated on the basis of the small polaron (SP) model with particular attention to the hopping and the coherent motions. They have been obtained in the forms: and , where d is a jump length, and Hd is a magnitude of internal dipolar field. At high temperatures, the activated-type hopping motion gives a dominant contribution to wD, and wS coincides with wD. With decreasing temperature, wD turns to be increasing owing to the coherent motion. Whereas wS deviates from wD, after passing the minimum, to have a maximum, and then decreases in inverse proportion to a lifetime (B) of the SP band states. Because of the cell periodicity of the internal fields, the spin in an SP band state feels a definite magnetic field corresponding to the state, and sees various fields if scattered to other states. These scattering processes succeeding in a time shorter than (γμHd)-1 result in the motional narrowing of the spectra, with λS ? γ2μHdB. 相似文献