Đang chuẩn bị liên kết để tải về tài liệu:
Synthesis and characterizations of novel thiazolyl-thiadiazole derivatives as telomerase activators

Không đóng trình duyệt đến khi xuất hiện nút TẢI XUỐNG

Pyridine-3/4-thiocarboxamide derivatives were used as starting materials for the synthesis of the target compounds. The pyridine-3/4-thiocarboxamide derivatives were reacted with ethyl 2-chloroacetoacetate in ethanol to give the thiazole derivatives (1, 2). The two ethyl thiazole-carboxylate derivatives (1, 2) thus obtained were treated with sodium hydroxide solution and ethanol and converted to carboxylic acids (3, 4). The carboxylic acid derivatives (3, 4) were reacted with thiosemicarbazide in phosphoroxy trichloride and aminothiadiazole rings (5, 6) were formed. Thus, two thiazolyl-thiadiazole amine derivatives (5, 6) were obtained. |

TÀI LIỆU LIÊN QUAN

The logic of chemical synthesis

ECE 551 Digital Design And Synthesis: Lecture 8

Summary of environmental technique doctoral thesis: Synthesis of silver, copper, iron nanoparticles and their applications in controlling cyanobacterial blooms in the fresh water body

Semi-synthesis of some heterocyclic triterpene derivatives on the basis of allobetulin

Challenges to qualitative evidence synthesis – Aiming for diversity and abstracting without losing meaning

Synthesis of nanozeolites and nanozeolite-based FCC catalysts, and their catalytic activity in gas oil cracking reaction

Lecture BSc Multimedia - Chapter 5: Digital audio synthesis

Advances in polymer based Friedlander quinoline synthesis

ECE 551 Digital Design And Synthesis: Lecture 9

Lecture Principles of biochemistry - Chapter 16 (part 4): Synthesis of eicosanoids, glycerolipids and isoprenoids
Đã phát hiện trình chặn quảng cáo AdBlock
Trang web này phụ thuộc vào doanh thu từ số lần hiển thị quảng cáo để tồn tại. Vui lòng tắt trình chặn quảng cáo của bạn hoặc tạm dừng tính năng chặn quảng cáo cho trang web này.