✦ LIBER ✦

Synthesis of the antifouling polyamine pseudoceratidine and its analogs: Factors influencing biocidal activity

✍ Scribed by James A Ponasik; Darren J Kassab; Bruce Ganem

Publisher: Elsevier Science
Year: 1996
Tongue: French
Weight: 176 KB
Volume: 37
Category: Article
ISSN: 0040-4039
DOI: 10.1016/0040-4039(96)01310-x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis and Biological Activities of t

Synthesis and Biological Activities of the Antibiotic B 371 and its Analogs

✍ Hoppe, Inga ;Schöllkopf, Ulrich 📂 Article 📅 1984 🏛 John Wiley and Sons 🌐 English ⚖ 380 KB

## Abstract The synthesis of the title compound **1** is described as well as the syntheses of a series of structural analogs of type **4**. The antimicrobial __in vitro__ activity of these vinyl isocyanides, substituted in β‐position either by an indole derivative or by an aryl or 2‐thienyl group,

A facile synthesis of an aldehydic analo

A facile synthesis of an aldehydic analog of platelet activating factor and its use in the production of specific antibodies

✍ Chang-jin Wang; Hsin-Hsiung Tai 📂 Article 📅 1990 🏛 Elsevier Science 🌐 English ⚖ 539 KB

The multistep synthesis of a platelet activating factor (PAF) analog having a reactive aldehyde group at the ~-end of the sn-I position is described. A novel ozonolysis of a double bond was employed to generate the aldehyde group in high yield under mild conditions. The aldehyde group was generated

Platelet-activating factor analogs. II.

Platelet-activating factor analogs. II. Synthesis of the 1-O-(4-decyloxymethylphenyl)- and 1-O-(4-decyloxyphenylmethyl) analogs

✍ R.C. Anderson; B.E. Reitter; C.M. Winslow 📂 Article 📅 1986 🏛 Elsevier Science 🌐 English ⚖ 472 KB

1-O-(4-Decyloxymethylphenyl)-and 1-O-(4-decyloxyphenylmethyl)-2-O-acetyl-glycero-3phosphorylcholine were synthesized from 2,2-dimethyl-l,3-dioxolane-4-methanol. The utility of a 2-O-tetrahydropyranyl ether as a protecting group and its facile removal in the pre~nce of a 3-phosphorylcholine is illust

A new method for the stereospecific synt

A new method for the stereospecific synthesis of ether phospholipids. Preparation of the amide analog of platelet-activating factor and related derivatives

✍ Nizal S Chadrakumar; Joseph Hajdu 📂 Article 📅 1982 🏛 Elsevier Science 🌐 French ⚖ 216 KB

A novel stereospecific synthesis of biologically active ether-phospholipids is reported. Ether phospholipids are among the most potent biologically active phospholipid derivatives.ls2 Naturally occuring as membrane-components, a number of l-sn-alkoxyglycero-phosphorylcholines have been shown to be r

Synthesis of an N-Acetylated Heparin Pen

Synthesis of an N-Acetylated Heparin Pentasaccharide and its anticoagulant activity in comparison with the heparin pentasaccharide with high anti-factor-Xa activity

✍ Hans Peter Wessel; Ludvik Labler; Thomas B. Tschopp 📂 Article 📅 1989 🏛 John Wiley and Sons 🌐 German ⚖ 714 KB

The synthesis of tri-N-acetylated heparin pentasaccharide 2 is described. It was assembled from five suitably blocked monosaccharide units (S7). Glucuronic-acid building block 4 was prepared from glucose by direct Jones oxidation of the 6-0-trityl derivative 18. The resulting acid 16 was esterified

Study of the crystal shape and its influ

Study of the crystal shape and its influence on the anti-tumor activity of tumor necrosis factor-related apoptosis-inducing ligand (Apo2L/TRAIL)

✍ Ji-Cheng Yin; Jin-Song Zhou; Jing Sun; Yi Qiu; Dong-Zhi Wei; Ya-Ling Shen 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 320 KB 👁 1 views

## Abstract This paper describes a method about the crystal shape control improving the anti‐tumor activity of tumor necrosis factor‐related apoptosis‐inducing ligand (Apo2L/TRAIL) in a batch cooling suspension crystallization by selecting pH values as a controllable variable. Three shaped TRAIL cr