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19篇 您的检索式:作者名="Laronze"
    题名 作者 年代 出处 被引量
1γ-甲基-1,4-戊内酯的新合成方法显示文摘以丙二酸和异丁醛为起始原料 ,通过 Knoevenagel缩合 ,再经异构化和内酯化反应合成了γ-甲基 - 1 ,4-戊内酯 ,总收率 53%张强 闻韧 Henin J Laronze J-Y 2000中国医药工业杂志2000,31,6:1
2The antitumor properties of the alpha 3 (Ⅳ)-(185-203) peptide from the NC1 domain of type Ⅳ collagen (tumstatin) are conformation-dependent显示文摘Floquet N Pasco S Ramont L Derreumaux P Laronze J Y Nuzillard J M 2004J Biol Chem2004,279,:1
3A novel strategy for designing specific gelatinase A inhibitors: potential use to control tumor progression 显示文摘Auge F Hornebeck W Laronze JY 2004Crit Rev Oncol Hematol2004,49,:1
4Rare earth fluorosulfides LnSF and Ln2AF4S2 as new colour pigments显示文摘Demourgues A Tressaud A Laronze H 2001Journal of Alloys and Compounds2001,,:1
5Prepara- tion and characterization of alkali- and alkaline earth- based rare earth sulfides显示文摘Laronze H Demourgues A Tressaud A 1998Journal of Alloys and Com- pounds1998,,:1
6A novel strategy for designing specific gelatinase A inhibitors: potential use to control tumor progression 显示文摘Auge F Homebeck W Laronze JY 2004Crit Rev Oncol Hematol2004,49,3:1
7Synthesis and anticancer activityof new pyrrolocarbazoles and(pyrrolo)-β-carbolines 显示文摘LARONZE M BOISBRUN M 2005Bioorg&Med Chem2005,13,:1
8Synthesis and anticancer activity of new pyrrolocarbazoles and pyrrolo-beta-carbolines显示文摘Laronze M Boisbrun M Leonce S 2005Bioorg Med Chem2005,13,:1
9A novel strategy for designing specific gelatinase inhibitors: potential use to control tumor progression显示文摘AUGE F HOMEBECK W LARONZE J Y 2004Crit Rev Oncol Hematol2004,49,3:1
10Synthesis and anticancer activity of new pyrrolocarbazoles and pyrrolo-β-carbolines显示文摘Laronze M Boisbrun M Leonce S 0,,06:1
11查看详情显示文摘Laronze N Marrot J Herv6 G 0,,:1
12A novel strategy for designing specific gelatinase inhibitors:potential use to control tumor progression显示文摘AUGE F HORNEBECK W LARONZE J Y 2004Crit Rev Oncol/Hematol2004,49,3:1
13Preparation and structural properties of new series of mixed - anion compounds: rare earth fluorosulfides显示文摘Demourgues A Tressaud A Laronze H 2001J of Fluorine Chemistry2001,107,:1
14The rearrangement of some cyclopentanone-aryloximes:synthesis of (±)aplysin,(±)filiformin and of their debromo analogues显示文摘Laronze JY Boukili RE Patigny D 0,,48:1
15Preparation and characterization of alkali- and alkaline earth-based rare earth sulfides 显示文摘Laronze H Demourgues A Tressaud A 1998Journal of Alloys and Compounds1998,275,277:1
16The rearrangement of some cyclopentanone-aryloximes:synthesis of (±)aplysin,(±)-filiformin and of their debromo analogues显示文摘Laronze Y Boukili R E Patigny D 1991Tetrahedron1991,47,10:1
17Collagen-binding domains of gelatinase A and thrombospondin-derived peptides impede endocytic clearance of active gelatinase A and promote HT1080 fibrosarcoma cell invasion显示文摘Robinet A Emonard H Banyai L Laronze J Y Patthy L Hornebeck W 2008Life Sci2008,82,78:1
18The reaarrangement of some cyclopentanone-aryloximes: synthesis of ( ± )-aplysin, ( ± ) -filiformin and of their debromo analogues 显示文摘J Y Laronze R E Boukili Dominique P 1991Tetrahedron1991,47,10:1
1914-羟基-去乙基Vincadifformine的仿生合成及重排显示文摘六氢氮杂革并[4,5-b]吲哚甲酸甲酯(8)和2-羟基-5-碘甲基-四氢呋喃(10),经Kuehne仿生反应生成14α-和14β-羟基-去乙基vincadifformine(5a和5b)。5b经脱水生成去乙基tabersonine(4)。5a在过氧酸、三苯膦、醋酸作用下可仿生氧化-重排成14α-羟基-去乙基长春胺(6a)及其16-差向异物构体(6b)(83%:17%)。闻韧 Laronze J. Y. Lvy J. 1991上海医科大学学报1991,18,2:0
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