Titlebook: Organic Chemistry from Retrosynthesis to Asymmetric Synthesis; Vitomir ?unji?,Vesna Petrovi? Perokovi? Book 2016 Springer International Pu

變更

書目名稱Organic Chemistry from Retrosynthesis to Asymmetric Synthesis影響因子(影響力)




書目名稱Organic Chemistry from Retrosynthesis to Asymmetric Synthesis影響因子(影響力)學(xué)科排名




書目名稱Organic Chemistry from Retrosynthesis to Asymmetric Synthesis網(wǎng)絡(luò)公開(kāi)度




書目名稱Organic Chemistry from Retrosynthesis to Asymmetric Synthesis網(wǎng)絡(luò)公開(kāi)度學(xué)科排名




書目名稱Organic Chemistry from Retrosynthesis to Asymmetric Synthesis被引頻次




書目名稱Organic Chemistry from Retrosynthesis to Asymmetric Synthesis被引頻次學(xué)科排名




書目名稱Organic Chemistry from Retrosynthesis to Asymmetric Synthesis年度引用




書目名稱Organic Chemistry from Retrosynthesis to Asymmetric Synthesis年度引用學(xué)科排名




書目名稱Organic Chemistry from Retrosynthesis to Asymmetric Synthesis讀者反饋




書目名稱Organic Chemistry from Retrosynthesis to Asymmetric Synthesis讀者反饋學(xué)科排名

FUME

Vitomir ?unji?,Vesna Petrovi? Perokovi?hlreichen Aufgaben und L?sungen.Dieses Buch richtet sich an Bachelor- und Lehramtsstudierende und vermittelt einen fundierten Aufbau der Zahlbereiche. Ausgehend von den natürlichen Zahlen werden systematisch die ganzen, rationalen, reellen und komplexen Zahlen bis?hin zu den Hamiltonschen Quaternion

意外的成功

Vitomir ?unji?,Vesna Petrovi? Perokovi?sen wird.Gut verst?ndlich, fachlich fundiert, kein ?Fachchin.Dieses Buch wirft einen kritischen Blick auf das Gendern. Wenn Sie sich mit geschlechtergerechter Sprache nicht anfreunden k?nnen, finden Sie hier zahlreiche – auch v?llig neue – Argumente dagegen. Aber auch als Freund*in des Genderns werd

壟斷

Vitomir ?unji?,Vesna Petrovi? Perokovi? real und virtuell.Vertrauen ist für eine funktionierende ?konomie so unabdingbar wie für eine funktionierende Gesellschaft. Dieses Buch stellt die gro?e Bedeutung des Vertrauens in Wirtschaft und Gesellschaft heraus. Es zeigt auf, wie Vertrauen funktioniert, worauf es gründet und welche Rolle es in

CLEFT

Disconnection, Synthons, Introductory Example,opan-1-ol is selected as an exemplary target molecule for retrosynthetic analysis and its (.)-enantiomer for asymmetric synthesis. Interconversions of oxygen functionalities are overviewed. The acidity of the C–H bond as a key property for C–C disconnections is indicated. Some historical and environ

卵石

Retrosynthetic Analysis of the Compounds with One Functional Group,isconnection of carbinols, alkenes, ketones and nitro compounds are discussed. Concepts of .-Diels–Alder and .-Wittig disconnections are presented and the mechanisms of reactions explained. Application of the Wittig reaction on the industrial scale is exemplified by the synthesis of the analog of .,

Cytology

,Stereoisomers and Stereoselective Reactions—“Departure into Third Dimension”, in organic molecules—are discussed. The kinetic control of enantioselective reactions and characteristics of enantioselective and diastereoslective reactions is presented. Asymmetric syntheses are exemplified by the hydrogenation of C=O and C=NR bonds in prochiral substrates catalyzed by organometa

截?cái)?/a>

Disconnection with Participation of Two Functional Groups,unctional groups is introduced. The favorable relation of oxygen functionalities in a 1,3- and 1,5-dioxygenated pattern supporting logical disconnections is demonstrated. The Mannich reaction, Michael addition and Robinson annelation are presented as synthetic approaches to this target molecule base

四指套

油膏

Retrosynthetic Consideration of Heterocyclic Structures,n the 1,2-, 1,3- and 1,4-position is presented. Their use in the cyclization of medium-large rings is exemplified. Retrosyntheses and syntheses of biologically active heterocyclic compounds, . .. and ., are presented. Cyclizations to three- to seven-membered heterocycles with one or more heteroatoms