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THE STRUCTURE OF ARMILLARIZIN,A NEW PROTOILLUDANE SESQUITERPENOID AROMATIC ESTER FROM ARMILLARIA MELLEA(VAHL.EX FR)QUEL. 被引量:8
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作者 Jun Shan YANG Ya Lun SU Yu Lan WANG Xiao Zhang FENG De Quan YU Xiao Tian LIANG Institute of Materia Medica,Chinese Academy of Medical Sciences,Beijing,100050 《Chinese Chemical Letters》 SCIE CAS CSCD 1990年第2期173-174,共2页
A new protoilludane sesquiterpenoid aromatic ester,named armillarizin (1)has been isolated from the artificially cultured mycelium of Armillaria me- llea(Vahl.ex Fr)Quel.(Tricholomataceae).Its structure was deduced on... A new protoilludane sesquiterpenoid aromatic ester,named armillarizin (1)has been isolated from the artificially cultured mycelium of Armillaria me- llea(Vahl.ex Fr)Quel.(Tricholomataceae).Its structure was deduced on the ba- sis of spectral analyses.The relative configuration was established from the nuclear Overhauser effects and from the values of ~1H-~1H coupling constants. 展开更多
关键词 FR THE structure OF ARMILLARIZIN A NEW PROTOILLUDANE SESQUITERPENOID AROMATIC ester FROM ARMILLARIA MELLEA VAHL.EX FR)QUEL
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Studies on the Relationship between the Helical Structure and Optical Activity of Some Chiral Cyclic Esters Ⅱ
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作者 Ai Hua NIE Xiu Lin YE Qi Yi XING(Department of Chemistry,Pcking University,Beijing 100871) 《Chinese Chemical Letters》 SCIE CAS CSCD 1997年第2期141-144,共4页
A method for the analysis of the relationship between the helical structure and optical activity was proposed by the study of the conformations and X-ray diffraction structures of some cyclic esters prepared by esteri... A method for the analysis of the relationship between the helical structure and optical activity was proposed by the study of the conformations and X-ray diffraction structures of some cyclic esters prepared by esterification of L-(-)-2.3-O-methylidene threitol and L-(+)-2,3-O-isopropplidene threitol with alkanedioyl dichlorides and o-,m-,and p-phthaloyl dichlorides. 展开更多
关键词 Activity CL Studies on the Relationship between the Helical structure and Optical Activity of Some Chiral Cyclic esters
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Structural effects of multiple-bonds on aggregating tendencies of long-chain esters 被引量:1
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作者 JIANG Xi-Kui JI Guo-Zhen LUO Guang-Lin 《Chinese Journal of Chemistry》 SCIE CAS CSCD 1991年第5期448-452,共0页
The kinetics of the hydrolysis of p-nitrophenyl esters of three types of single-chain carbo- xylic acids, namely, saturated, olefinic and acetylenic, was investigated in two aquiorgano binary sol- vent systems, DMSO-H... The kinetics of the hydrolysis of p-nitrophenyl esters of three types of single-chain carbo- xylic acids, namely, saturated, olefinic and acetylenic, was investigated in two aquiorgano binary sol- vent systems, DMSO-H_2O and dioxane (DX)-H_2O. The ester probes used are: octanoie (C8), do- decanoic (C12), stearic (C18), oleic (C18-ol), elaidic (C18-el) and stearolic (C18-st). The order of measured CAgC values is: C18-ol>C18-el>C18>C18-st, whereas the order of decreasing magnitude of the observed hydrolytic rate constants of the monomeric species (km) is: C18 >C18-el>C18-ol> C18-st. These rather unanticipated results are discussed. 展开更多
关键词 Structural effects of multiple-bonds on aggregating tendencies of long-chain esters
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