云南“生态茶”的化学成分

从云南西双版纳产大叶茶（Ｃａｍｅｌｌｉａｓｉｎｅｎｓｉｓｖａｒ．ａｓｓａｍｉｃａ）制成的“生态茶”中分离到１１个化合物和１个混晶,经光谱测定,１１个化合物分别鉴定为没食子酸、（＋）儿茶素、（－）表儿茶素、（－）没食子儿茶素、（－）表没食子儿茶素、（－）表儿茶素－３－０没食子酸酯、（－）表没食子儿茶素－３－Ｏ没食子酸酯、茶素、１,４,６－三役食子酰基－β－Ｄ葡萄糖１－Ｏ－没食子酰基－４,６－（－）－六羟基联苯二甲醚基－β－Ｄ－葡萄糖以及咖啡因;混晶为芦丁和山奈酚－３－芸香糖甙的混合物。这是对国产大叶茶的第一次较详细的化学研究。     

白蔹单宁化学成分的研究

从白蔹Ａｍｐｅｌｏｐｓｉｓ ｊａｐｏｎｉｃａ（Ｔｈｕｎｍｂ．）Ｍａｋｉｎｏ的乙酸乙酯提取物中分离出５个单宁化合物。经光谱分析和化学方法鉴定,它们为没食子酸（ｇａｌｌｉｃ ａｃｉｄ,１）,１,２,６－三氧－没食子酰基－β－Ｄ－吡喃葡萄糖（１,２,６－ｔｒｉ－Ｏ－ｇａｌｌｏｙ１－β－Ｄ－ｇｌｕｃｏｐｙｒａｎｏｓｉｄｅ,２）,１,２,３,６－四氧－没食子酰基－β－Ｄ－吡喃葡萄糖（１,２,４,６－ｔｅｔｒ     

滇黄芩中五个新的黄酮类配糖体

从滇黄芩（Ｓｃｕｔｅｌｌａｒｉａ ａｍｏｅｎａ）根中分离到５个新的黄酮类配糖体。命名为滇黄芩甙甲－戊（ａｍｏｅｎｉｎｓＡ－Ｅ）。经光谱分析,化学结构分别证明为：２’,４’,６’－三羟基二氢查耳酮４’－「Ｏ－β－Ｄ－半乳吡喃糖基（１→２）」－Ｏ－β－Ｄ－葡萄吡喃糖甙,５,７,２’－三羟基－６－甲氧基二氢黄酮７－Ｏ－β－Ｄ－葡萄吡喃糖醛酸甙,（顺式）－５,７,２’－三羟基二氢黄酮醇３－Ｏ－β－Ｄ－葡萄     

鞭打绣球中的苯丙素甙和环烯醚萜甙

从鞭打绣球（ＨｅｍｉｐｈｒａｇｍａｈｅｔｅｒｏｐｈｙｌｌｕｍＷａｌｌ．）（玄参科）的全草中分离到２个新的苯丙素甙,命名为鞭打绣球甙Ａ和Ｂ（ｈｅｍｉｐｈｒｏｓｉｄｅＡａｎｄＢ）,２个已知的苯丙素甙,ｐｌａｎｔａｍａｊｏｓｉｄｅ和ｐｌａｎｔａｉｎｏｓｉｄｅＤ,以及３个已知的环烯醚萜甙,ｇｌｏｂｕｌａｒｉｃｉｓｉｎ,ｇｌｏｂｕｌａｒｉｎ和ｉｓｏ－ｓｃｒｏｐｈｕｌａｒｉｏｓｉｄｅ．通过化学和光谱分析,鞭打绣球甙Ａ和Ｂ的结构分别鉴定为２－（３－羟基－４－甲氧基苯基）乙基０－β－Ｄ－葡萄吡喃糖基（１→３）－４－Ｏ－反式阿魏醚基－β－Ｄ－葡萄吡喃糖试和２－（３,４－二羟基苯基）乙基Ｏ－［６－Ｏ－乙醚基－β－Ｄ－葡萄吡喃糖基（１→３）］－４－Ｏ－反式咖啡醚基－β－Ｄ－葡萄吡喃糖甙．     

滇重楼地上部分的配糖体

从滇重楼ＰａｒｉｓｐｏｌｙｐｈｙｌｌａＳｍ．ｖａｒ．ｙｕｎｎａｎｅｎｓｉｓ（Ｆｒ．）Ｈ－Ｍ,地上部分,分离出４个微量的配糖体,经光谱分析和化学降解证明其化学结构分别为２５Ｓ－异钮替皂甙元－３－Ｏ－α－Ｌ－鼠李吡喃糖基（１→２）［α－Ｌ－鼠李吡喃糖基（１→４）］－β－Ｄ－葡萄吡喃甙（Ａ）,２６－β－Ｄ－葡萄吡喃糖基－纽替皂甙元－３－Ｏ－α－Ｌ－鼠李吡喃糖基（１→２）［α－Ｌ－鼠李吡喃糖基（１→４）－β－Ｄ－葡萄吡喃糖甙（Ｂ）,山奈酚－３－Ｏ－β－Ｄ－葡萄吡喃糖基（１→６）－β－Ｄ－葡萄吡喃甙（Ｃ）,７－Ｏ－α－Ｌ－鼠李吡喃糖基－山奈酚－３－Ｏ－β－Ｄ－葡萄吡喃糖基（１→６）－β－Ｄ－葡萄糖甙（Ｄ）。     

仙茅根茎中的配糖体

从仙茅（ Ｃｕｒｃｕｌｉｇｏ ｏｒｃｈｉｏｉｄｅｓＧａｅｒｔｎ） 根茎中分离到７ 个化合物, 经光谱分析推定其化学结构分别为： ２, ６ － 二甲氧基苯甲酸（Ａ） ; 苔黑酚葡萄糖甙（Ｂ） ; 仙茅素Ａ （Ｃ） ; 仙茅甙（Ｄ） ; ２４ｓ, ３β, １１α, １６β, ２４ － 四羟基环阿尔廷醇－ ３ － Ｏ－ α－ Ｌ－ 鼠李吡喃糖基（１ →２） － β－Ｄ－ 葡萄吡喃糖甙（Ｅ） ; ２４ｓ, ３β, １１α, １６β, ２４ － 四羟基环阿尔廷醇－ ３－ Ｏ－ β－ Ｄ－ 葡萄吡喃糖基（１ →２） － β－ Ｄ－ 葡萄吡喃糖甙（Ｆ） 和胡萝卜甙（Ｇ） 。Ｆ为一新甙。     

闭鞘姜根中的甾体皂甙

从闭鞘姜「Ｃｏｓｔｕｓ ｓｐｅｃｉｏｓｕｓ（Ｋｏｅｎｉｇ）Ｓｍｉｔｈ」根茎中分离出五个化合物。经波谱解析和化学降解,证明其化学结构分别为胡萝卜甙（Ａ）：薯芋皂甙元３－Ｏ－ａ－Ｌ鼠李吡喃糖基（１－２）－β－Ｄ－葡萄吡喃糖甙（Ｂ）;薯芋皂甙元３－Ｏ－ａ－Ｌ－鼠李吡喃糖基（１－２）「ａ－Ｌ－鼠李吡喃糖基（１－４）」β－Ｄ葡萄吡喃糖甙（Ｃ）;薯芋皂甙元－３－Ｏ－ａ－Ｌ－鼠李吡喃糖基（１－２）「β－Ｄ－葡萄     

蜘蛛抱蛋根茎中的甾体皂甙

从蜘蛛抱蛋（ＡｓｐｉｄｉｓｔｒａｅｌａｔｉｏｒＢｌ．）根茎的甲醇提取物中分离得两个甾体皂甙。经波谱解析及化学降解证明其化学结构分别为薯芋皂甙元一３一Ｏ－［Ｂ－Ｄ－葡萄吡喃糖基（１→２）］－［Ｂ－Ｄ－木吡喃糖基（１→３）］－Ｂ－Ｄ－葡萄吡喃糖基（１→４）－Ｂ－Ｄ一半乳吡喃糖甙（即蜘蛛抱蛋甙ａｓｐｉｄｉｓｔｒｉｎ）及新静诺特皂甙元－３－Ｏ－［Ｂ－Ｄ－葡萄吡喃糖基（１→２）］～［Ｂ－Ｄ－木吡喃糖基（１→３）－Ｂ－Ｄ－葡萄吡喃糖基（１→４）一Ｂ－Ｄ－半乳吡喃糖甙,后者为一新试,命名为新蜘蛛抱蛋甙ｒｅｏａｓｐｉｄｉｓｔｒｉｎ。     

滇重楼地上部分的两个微量皂甙

从滇重楼地上部分中分离出两个新的微量的甾体皂甙ＰｏｌｙｐｈｙｌｌｏｓｉｄｅⅢ和Ⅳ,根据化学降解和光谱分析,它们的化学结构分别为２７－羟基－偏诺皂皂甙元－３－Ｏ［ａ－Ｌ－鼠李吡喃糖基（１→２）］［ａ－Ｌ－鼠李吡喃糖基（１→４－ａ－Ｌ鼠李吡喃糖基（１→４）］－β－Ｄ－葡萄吡喃糖甙,２３β,２７－二羟基－偏皂甙元－３－Ｏ－［ａ－鼠李吡喃糖（１→２）］     

婆婆针的化学成分

婆婆针（ＢｉｄｅｎｓｂｉｐｉｎｎａｔａＬｉｎｎ）是具有清热解毒功能的民间药用植物,从婆婆针的地上部分分离鉴定了３个苯丙素甙类化合物,４－Ｏ－（６″－Ｏ－对香豆酰基－β－吡喃葡萄糖）－对－香豆酸（１）,４－Ｏ－（２″－Ｏ－乙酰基－６″－Ｏ－对－香豆酰基－β－Ｄ－吡喃葡萄糖）－对－香豆酸（２）及４－Ｏ－（２″,４″－Ｏ－二乙酰基－６″－Ｏ－对－香豆酰基－β－Ｄ－吡喃葡萄糖）－对－香豆酸（３）,其中（３     

Synthesis and chemical behaviour of D-glucosyl esters of glutamic acid having the side-chain carboxyl group involved in the glycosidic linkage.

Simultaneous and stepwise deprotection of the fully benzylated D-glucosyl esters of 1-benzyl N-benzyloxycarbonyl- and N-tert-butyloxycarbonyl-L-glutamic acid (1 and 5, respectively) have been examined. Catalytic hydrogenation of 1 led to intramolecular aminolysis to give pyroglutamic acid and D-glucose, but similar treatment in the presence of trifluoroacetic acid afforded both anomers of 1-O-(L-gamma-glutamyl)-D-glucopyranose, which were characterized as trifluoroacetates (2alpha and 2beta) and converted into 2,3,4,6-tetra-O-acetyl-1-O-[1-methyl N-(acetyl)-L-glutam-5-oyl]-D-glucopyranose (4) which was also prepared by a definitive method. Hydrogenolysis of 5 gave both anomers of 1-O-[N-(tert-butyloxycarbonyl)-L-gamma-glutamyl]-D-glucopyranose (6), which, upon treatment with trifluoroacetic acid at - 10 degrees, afforded 2alpha and 2beta, respectively. The structure of 6beta was established by its conversion into 2,3,4,6-tetra-O-acetyl-1-O-[1-methyl N-(tert-butyloxycarbonyl)-L-glutam-5-oyl]-beta-D-glucopyranose (7beta), whereas similar treatment of 6alpha gave a mixture of 1,3,4,6-tetra-O-acetyl-2-O-[1-methyl N-(tert-butyloxycarbonyl)-L-glutam-5-oyl]-alpha-D-glucopyranose (9) and 7alpha. A 1 leads to 2 acyl migration occurred during esterification of the aglycon carboxyl group of 6alpha with diazomethane to give 2-O-[1-methyl N-(tert-butyloxycarbonyl)-L-glutam-5-oyl]-alpha-D-glucopyranose (8).     

金铁锁的两个新三萜皂苷

从石竹科植物金铁锁(Psammosilene tunicoides W．C．Wu et C．Y．Wu)根部分离得到4个齐墩果酸型五环三萜皂苷。它们的结构通过波谱和化学方法分别鉴定为：3-O-β-D-galac-topyranosyl-(1→2 )-β-D-6-O-methylgtucuronopymnosyl-quillaic acid (1),3-O-β-D-galactopymnosyl-(1→2)-[β-D-xylopyranosyl-(1→3)]-β-D-gtucuronopyranosyl-quillaic acid (2),3-O-β-D-galactopyrano-syl-(1→2)-[β-D-xylopyranosyl-(1→3)]-β-D-6-O-methylgtucuronopyranosyl-quillaic acid(3),3-O-β-D-galactopymnosyl-(1→2)-[β-D-xylopyranosyl-(1→3)]-β-D-6-O-ethylgtucuronopyranosyl-quillaic acid(4)。其中1为木鳖子中发现的次甙,3和4为新化合物。     

Phenolic derivatives from Ruprechtia polystachya and their inhibitory activities on the glucose-6-phosphatase system

Two new compounds, 5-methyl-2-(2-methylbutanoyl)phloroglucinol 1-O-(6-O-β-D-apiofuranosyl)-β-D-glucopyranoside (1) and trans-2,3-dihydrokaempferol 3-O-(4-O-sulfo)-α-L-arabinopyranoside (2), together with 14 known flavonoids, trans-dihydrokaempferol 3-O-α-L-arabinopyranoside (3), trans-taxifolin 3-O-α-L-arabinofuranoside (4), quercetin 3-O-α-L-rhamnopyranoside (5), quercetin 3'-O-α-L-arabinofuranoside (6), catechin 3-O-α-L-rhamnopyranoside (7), trans-taxifolin 3-O-α-L-arabinopyranoside (8), cis-dihydrokaempferol 3-O-α-L-arabinopyranoside (9), catechin (10), myricetin 3-O-α-L-rhamnopyranoside (11), quercetin 3-O-α-L-arabinopyranoside (12), quercetin 3-O-α-L-arabinofuranoside (13), quercetin 3-O-(3″-galloyl)-α-L-rhamnopyranoside (14), quercetin 3-O-(2″-galloyl)-α-L-rhamnopyranoside (15), and epicatechin 3-O-gallate (16), were isolated from the leaves of Ruprechtia polystachya Griseb. (Polygonaceae). Their structures were established on the basis of extensive 1D- and 2D-NMR experiments as well as MS analyses. All compounds, except 1, showed inhibition of the enzyme glucose-6-phosphatase in intact microsomes.     

古蔺雪胆中的新三萜皂苷

从采自四川汉源县的古蔺雪胆(Hemsleya penxianensis var.gulinensiks)中分到9个三萜皂苷化合物,通过化学反应和光谱方法鉴定了它们的结构。其中7个为已知化合物,分别为齐墩果酸-28-O-β-D-比喃葡萄糖苷(1),3-O-β-D-吡喃葡萄糖醛基齐墩果酸苷(3),3-O-β-D-吡喃葡萄糖醛基—齐墩果酸—28-O-α-L-吡喃阿拉伯糖苷(4),3-O-β-D-吡喃葡萄糖醛基—齐墩果酸—28-O-β-D-吡喃葡萄糖苷(5),3-O-α-L-阿拉伯糖基—(1→3)—β—D-吡喃葡萄糖醛基—齐墩果酸—28—O—β—D—吡喃葡萄糖苷(6),3—O—(6′—丁酯)—β-D-吡喃葡萄糖醛基—齐墩果酸—28-O-α-L-阿拉伯糖苷(7),3-O-(6′-丁酯)—β—D吡喃葡萄糖醛基—齐墩果酸—28-O-β-D-吡喃葡萄糖苷(8)。两个新化合物,即雪胆皂苷A(2)和雪胆皂苷B(9)。     

云南金钱槭茎化学成分

对云南金钱槭枝条部分的化学成分进行了研究,从其乙醇提取物中共分离鉴定了16个化合物,通过波谱学方法鉴定为:erythro-4,7,9-三羟基-3,3'-二甲氧基-8-O-4'-新木脂素-9'-O-β-D-吡喃葡萄糖苷(1),Hyugano-side IIIa(2),Hyuganoside IIIb(3),erythro-Buddlenol B(4),erythro-7',8'-Didehydrobuddlenol B(5),(±)-丁香脂素(6),臭矢菜素A(7),柑橘苷A(8),(4R)-p-薄荷-1-烯-7,8-二醇7-O-β-D-吡喃葡萄糖苷(9),2-甲氧基-3-(3-吲哚基)丙酸(10),肌苷(11),Tachioside(12),Isotachioside(13),3-O-(β-D-吡喃葡萄糖基)-1-(3,5-二甲氧基-4-羟基苯基)-1-丙酮(14),反式异松柏苷(15),4-[(E)-3-乙氧基-1-丙烯基]-2-甲氧基苯酚(16)。其中化合物5为新的倍半木脂素,其余化合物均首次从该属植物中分离得到。     

中国植物区系的性质和各成分间的关系

根据植物区系平衡理论,以“中国种子植物区系研究”项目的结果材料分析中国植物区系的性质和各成分间的关系。从全国整体来看,中国植物区系是亚热带性质,热带成分和温带成分分别占50.2%和49.8%,即基本平衡。而各地区间有显著差异,文中做了具体比较分析及揭示其变化规律,大致是热带成分在热带地区占75%～85%,亚热带地区占40%～60%,温带地区占15%～25%,寒温,高寒和中亚荒漠地区占5%～10%,自南向北向西方向递减,温带成分与之相反,而且北方温带成分变化曲线与热带成分呈反射状,表明二者是以相反方向同等发展的。文中又据中国种子属15个分布型或地理成分所归科的相似性系数矩阵来研究各成分间的关系,结果是相似性系数为12～58强,分为10级（10～60）,排列出各成分间相似性程度及其变化梯度,其中以东亚和中国特有成分间关系最密切,温带亚洲和热带亚洲间关系最疏远,同时显出3个关系很密及最密区域,即旧大陆热带,古地中海和东亚,这三区域里可能是中国植物区系的发源地。     

桂火绳中化学成分的研究

从梧桐科火绳属桂火绳中提取分离到22个化合物,经结构鉴定为:羽扇豆醇(1),白桦脂酸(2),齐墩果酸(3),丁香脂素(4),(+)-异落叶松树脂醇(5),东莨菪内酯(6),对羟基肉桂酸(7),二十七碳酸单甘油酯(8),2-十八烯酸单甘油酯(9),sitoindosideⅡ(10),儿茶素(11),表儿茶素(12),表儿茶素3-O-β-D-吡喃木糖甙(13),山奈酚3-O-β-D-吡喃葡萄糖甙(14),5,7,4'-三羟基异黄酮(15),4'-O-methylgallocatechin(16),反式-二氢槲皮素-3-O-α-阿拉伯糖甙(17),顺式-二氢槲皮素-3-O-α-阿拉伯糖甙(18),反式-二氢槲皮素-3-O-β-吡喃葡萄糖甙(19),3,5,7,3',5'-五羟基-4'-甲氧基异黄酮(20),山奈酚-3-O-β-D-吡喃葡萄糖(6→1)-α-L-吡喃鼠李糖甙(21),以及槲皮素3-O-β-D-吡喃葡萄糖(6→1)-β-D-吡喃葡萄糖甙(22),这些化学成分首次从该属植物中分离出来。     

鹿蹄草化学成分研究

从鹿蹄草(Pyrola callianthaH.Andres)中分离得到11个化合物,经光谱分析确定其结构为(4R)-1-四氢萘酮(1),(4S)-1-四氢萘酮(2),夹竹桃麻素(3),没食子酸(4),3,4-二羟基苯甲酸(5),鹿蹄草素(6),5-羟甲基糠醛(7),金丝桃苷(8),2″-O-没食子酰基金丝桃苷(9),鹿蹄草苷B(10),4-羟基-2,7-二甲基萘基-1-O-β-D-吡喃葡萄糖苷(11)。其中化合物1,2,3,5,6,11为首次从该植物中分离得到,化合物7为首次从该属中分离得到。     

小金梅草化学成分研究(英文)

从小金梅草乙醇提取物中分离得到了12个化合物,分别为3-O-β-D-槲皮素葡萄糖苷(1)、3-O-β-D-山柰酚葡萄糖苷(2)、5-O-β-D-芹菜素葡萄糖苷(3)、α-菠甾醇(4)、2,6-二甲氧基苯甲酸(5)、3-吲哚甲酸(6)、(2S,3R,4E,8E)-1-(β-D-吡喃葡萄糖苷)-N-[(R)-2’-羟基-二十碳酰基]-9-甲基-4,8-二烯-1,3-二醇-2-氨基-十八烷(7)、正三十二烷醇(8)、14,15-二十碳烯酸(9)、木腊酸(10)、β-谷甾醇(11)、胡萝卜苷(12)。以上化合物均为首次从该植物中得到。     

Synthesis and rearrangements of D-glucosyl esters of aspartic acid linked through the 1- or 4-carboxyl group.

Catalytic hydrogenation of 2,3,4,6-tetra-O-benzyl-1-O-[1-benzyl N-(benzyloxycarbonyl)-L-aspart-4-oyl]-alpha-D-glucopyranose (1alpha) in acetic acid-2-methoxyethanol gave 1-O-(L-beta-aspartyl)alpha-D-glucopyranose (2alpha) contaminated with 2-O-(L-alpha-aspartyl)-D-glucopyranose (8). Evidence that 8 was formed from the 1-oyl isomer of 1alpha, namely 2,3,4,6-tetra-O-benzyl-1-O-[4-benzyl N-(benzyloxycarbonyl)-L-aspart-1-oyl]-alpha-D-glucopyranose (7alpha), via 1 leads to 2 acyl migration, was obtained by submitting the deprotected D-glucosyl ester to successive N-acetylation, esterification, and O-acetylation; the final product was identified as a approximately 4:1 mixture of 2,3,4,6-tetra-O-acetyl-1-O-[1-methyl N-(acetyl)-L-aspart-4-oyl]-alpha-D-glucopyranose (4alpha) and 1,3,4,6-tetra-O-acetyl-2-O-[4-methyl N-(acetyl)-L-aspart-1-oyl]-D-glucopyranose (6) which were also prepared by definitive methods. On the other hand, deprotection of 1beta gave isomerically pure 2beta which was converted into the peracetylated ester derivative 4beta; an explanation for the differences in aglycon isomeric purity of 2alpha and 2beta is given. Hydrogenolysis of 7beta under the above conditions led to intermolecular transesterification with scission of the C-1 ester bond to give 1-(2-methoxyethyl) L-aspartic acid and D-glucose. Catalytic hydrogenation of 7alpha and 7beta, performed in the presence of trifluoroacetic acid, afforded 1-O-(L-alpha-aspartyl)-alpha- and -beta-D-glucopyranoside trifluoroacetate salts (11alpha and 11beta), respectively. The structure of 11beta was established by successive conversion into 2,3,4,6-tetra-O-acetyl-1-O-[4-methyl N-(acetyl)-L-aspart-1-oyl]-beta-D-glucopyranose (5beta) which was also prepared by definitive methods. Analogous treatment of 11alpha gave the N-acetyl derivative 12 which underwent 1 leads to 2 acyl migration during esterification with diazomethane to give the N-acetyl methyl ester derivative 10; acetylation of 10 afforded 6.