Titlebook: Bioactive Heterocycles II; Shoji Eguchi Book 2007 Springer-Verlag Berlin Heidelberg 2007 Pericyclic reaction.Pyrimidine.biochemistry.chemi

Opiate

書目名稱Bioactive Heterocycles II影響因子(影響力)




書目名稱Bioactive Heterocycles II影響因子(影響力)學科排名




書目名稱Bioactive Heterocycles II網(wǎng)絡(luò)公開度




書目名稱Bioactive Heterocycles II網(wǎng)絡(luò)公開度學科排名




書目名稱Bioactive Heterocycles II被引頻次




書目名稱Bioactive Heterocycles II被引頻次學科排名




書目名稱Bioactive Heterocycles II年度引用




書目名稱Bioactive Heterocycles II年度引用學科排名




書目名稱Bioactive Heterocycles II讀者反饋




書目名稱Bioactive Heterocycles II讀者反饋學科排名

Isolate

Ring Transformation of Nitropyrimidinone Leading to Versatile Azaheterocyclic Compounds,pyridone and nitropyrimidinone are excellent substratesfor this reaction. Dinitropyridone behaves as the synthetic equivalent of unstable nitromalonaldehyde togive nitroanilines, nitropyridines, and nitrophenols. On the other hand, nitropyrimidinone causes threekinds of RTF reactions. When nitropyri

MORPH

Synthesis of Thalidomide,its formulation in 1956. While most of the early studiesspecifically concerned teratogenicity, recently there has been a?resurgence of interest in thalidomidebecause of its potential for treating a?number of otherwise intractable diseases, such as leprosy,human immunodeficiency virus replication in

blister

chiropractor

bypass

Intractable

CARK

JavaScript Programmer‘s Referenceoline,has two structural features: a?.-fused bicyclic heterocycleand a?quaternary carbon stereocenter at the bridgehead position. Syntheses of the intermediate ketonereported by some research groups are described. The synthesis of chiral TNA-67 is also shown.

大廳

Rational Drug Design of , Opioid Receptor Agonist TAN-67 from , Opioid Receptor Antagonist NTI,oline,has two structural features: a?.-fused bicyclic heterocycleand a?quaternary carbon stereocenter at the bridgehead position. Syntheses of the intermediate ketonereported by some research groups are described. The synthesis of chiral TNA-67 is also shown.

LAVA

https://doi.org/10.1007/978-1-4842-1787-0ocycles related to biologically interesting molecules. The article also extends to ionic reactionsin a?similar fashion, though not many examples have been investigated. The scope and limitations arealso described when necessary.