標(biāo)題: Titlebook: Organolithiums in Enantioselective Synthesis; David M. Hodgson Book 2003 Springer-Verlag Berlin Heidelberg 2003 Metalorganic Chemistry.che [打印本頁(yè)] 作者: PEL 時(shí)間: 2025-3-21 17:56
書(shū)目名稱(chēng)Organolithiums in Enantioselective Synthesis影響因子(影響力)
書(shū)目名稱(chēng)Organolithiums in Enantioselective Synthesis影響因子(影響力)學(xué)科排名
書(shū)目名稱(chēng)Organolithiums in Enantioselective Synthesis網(wǎng)絡(luò)公開(kāi)度
書(shū)目名稱(chēng)Organolithiums in Enantioselective Synthesis網(wǎng)絡(luò)公開(kāi)度學(xué)科排名
書(shū)目名稱(chēng)Organolithiums in Enantioselective Synthesis被引頻次
書(shū)目名稱(chēng)Organolithiums in Enantioselective Synthesis被引頻次學(xué)科排名
書(shū)目名稱(chēng)Organolithiums in Enantioselective Synthesis年度引用
書(shū)目名稱(chēng)Organolithiums in Enantioselective Synthesis年度引用學(xué)科排名
書(shū)目名稱(chēng)Organolithiums in Enantioselective Synthesis讀者反饋
書(shū)目名稱(chēng)Organolithiums in Enantioselective Synthesis讀者反饋學(xué)科排名
作者: 系列 時(shí)間: 2025-3-21 21:06 作者: lanugo 時(shí)間: 2025-3-22 03:35 作者: ADOPT 時(shí)間: 2025-3-22 07:30
Enantioselective Synthesis by Lithiation Adjacent to Nitrogen and Electrophile Incorporation, with a single chiral ligand and diastereoselective and enantioselective conjugate additions with benzylic and allylic lithiation intermediates. The sequences are classified, where information is available, in terms of stereocontrol in the lithiation or substitution step.作者: crescendo 時(shí)間: 2025-3-22 09:31
Book 2003n inspiration for future developments. Following an overview chapter summarising the key milestones, successive chapters, each written by leading experts in their field, critically survey all the major areas of progress..作者: DUST 時(shí)間: 2025-3-22 14:51 作者: 衣服 時(shí)間: 2025-3-22 17:06
Enantioselective Conjugate Addition and 1,2-Addition to C=N of Organolithium Reagents,ine chemistry is also briefly presented. Sect. 2 summarizes the 1,2-additions to imines and imine congeners (hydrazones, oxime ethers, nitrones) using chiral auxiliaries and chiral ligands. We do not describe additions which use chiral auxiliary groups in carbonyl compounds.作者: 忘恩負(fù)義的人 時(shí)間: 2025-3-23 01:11 作者: QUAIL 時(shí)間: 2025-3-23 02:20
Enantioselective Addition of Organolithiums to C=O Groups and Ethers,es and ketones) or enantioselective cleavages of C-O units in strained ethers (i.e., epoxides and oxetanes) as well as in acetals. The achievement of high enantioselectivities is desirable and hence factors controlling these enantioselectivities are subjects of intensive research. Beneficial externa作者: Myosin 時(shí)間: 2025-3-23 07:11
Enantioselective Conjugate Addition and 1,2-Addition to C=N of Organolithium Reagents, reactions of organolithium reagents constitutes a remarkable area of fundamental progresses in recent synthetic organic chemistry. The conjugate addition (or Michael reaction, 1,4-addition) and 1,2-addition to C= N double bonds are powerful methods for forming a carbon-carbon bond. This chapter rev作者: 騎師 時(shí)間: 2025-3-23 10:47 作者: Outmoded 時(shí)間: 2025-3-23 17:15 作者: Entirety 時(shí)間: 2025-3-23 20:13
Enantioselective Synthesis by Lithiation Adjacent to Oxygen and Subsequent Rearrangement,s field is presented. The first section concerns asymmetric Wittig rearrangements. Asymmetric retro-Brook rearrangements are then covered, followed by rearrangements of phosphate to phosphonate. The last section reviews asymmetric rearrangements of lithiated epoxides.作者: 愛(ài)好 時(shí)間: 2025-3-24 00:00
Enantioselective Synthesis by Lithiation to Generate Planar or Axial Chirality,laying these stereochemical features are ferrocenes, arenechromium tricarbonyl complexes, biaryls, atropisomeric amides and allenes. Methods for the enantioselective lithiation of these compound classes, relying on either substrate (chiral auxiliary) or reagent (chiral base) control will be reviewed作者: CODA 時(shí)間: 2025-3-24 03:26 作者: capillaries 時(shí)間: 2025-3-24 09:28 作者: acrophobia 時(shí)間: 2025-3-24 12:32 作者: 攝取 時(shí)間: 2025-3-24 18:49
Bernd Goldfusssly underestimate and misrepresent progress in managing various central nervous system tumors, the tremendous technologic enhancements that have revolutionized the imaging of the tumors and the host organ, the multitude of surgical adjuncts such as computerized imaging guidance and functional mappin作者: minimal 時(shí)間: 2025-3-24 22:56
Mayu Iguchi,Ken-ichi Yamada,Kiyoshi Tomiokasly underestimate and misrepresent progress in managing various central nervous system tumors, the tremendous technologic enhancements that have revolutionized the imaging of the tumors and the host organ, the multitude of surgical adjuncts such as computerized imaging guidance and functional mappin作者: 摸索 時(shí)間: 2025-3-25 02:21 作者: 聯(lián)想記憶 時(shí)間: 2025-3-25 07:03 作者: 留戀 時(shí)間: 2025-3-25 09:19
Takeshi Toru,Shuichi Nakamurasly underestimate and misrepresent progress in managing various central nervous system tumors, the tremendous technologic enhancements that have revolutionized the imaging of the tumors and the host organ, the multitude of surgical adjuncts such as computerized imaging guidance and functional mappin作者: Prognosis 時(shí)間: 2025-3-25 13:27
David M. Hodgson,Katsuhiko Tomooka,Emmanuel Grassly underestimate and misrepresent progress in managing various central nervous system tumors, the tremendous technologic enhancements that have revolutionized the imaging of the tumors and the host organ, the multitude of surgical adjuncts such as computerized imaging guidance and functional mappin作者: 生氣的邊緣 時(shí)間: 2025-3-25 18:20 作者: 縱欲 時(shí)間: 2025-3-25 23:46 作者: florid 時(shí)間: 2025-3-26 01:27 作者: 衍生 時(shí)間: 2025-3-26 06:06 作者: Dawdle 時(shí)間: 2025-3-26 09:43 作者: 合乎習(xí)俗 時(shí)間: 2025-3-26 13:58
Jonathan Claydencoveries have ushered in the era of molecular targeted therapy, as first demonstrated by the extraordinary success story in chronic myelogenous leukemia of imatinib (Gleevec). The rational combination of target978-0-387-29201-4978-0-387-29202-1作者: 觀點(diǎn) 時(shí)間: 2025-3-26 20:42
Jean F. Normantcoveries have ushered in the era of molecular targeted therapy, as first demonstrated by the extraordinary success story in chronic myelogenous leukemia of imatinib (Gleevec). The rational combination of target978-0-387-29201-4978-0-387-29202-1作者: 南極 時(shí)間: 2025-3-26 21:18 作者: 鋪?zhàn)?nbsp; 時(shí)間: 2025-3-27 04:56 作者: GRILL 時(shí)間: 2025-3-27 09:18 作者: 強(qiáng)行引入 時(shí)間: 2025-3-27 13:02 作者: Colonnade 時(shí)間: 2025-3-27 14:28 作者: GREEN 時(shí)間: 2025-3-27 17:49
Takeshi Toru,Shuichi Nakamuraof brain tumors, their proliferation, and their resistance to therapy. These molecular discoveries have ushered in the era of molecular targeted therapy, as first demonstrated by the extraordinary success story in chronic myelogenous leukemia of imatinib (Gleevec). The rational combination of target作者: accrete 時(shí)間: 2025-3-27 23:35
David M. Hodgson,Katsuhiko Tomooka,Emmanuel Grasof brain tumors, their proliferation, and their resistance to therapy. These molecular discoveries have ushered in the era of molecular targeted therapy, as first demonstrated by the extraordinary success story in chronic myelogenous leukemia of imatinib (Gleevec). The rational combination of target作者: 制定 時(shí)間: 2025-3-28 05:17
Enantioselective Synthesis by Lithiation Adjacent to Oxygen and Electrophile Incorporation, common, depending on the individual situation. 1-Oxy-2-alkenyllithium reagents have similar stereochemical properties. In a number of cases configurational stability is recorded. Procedures for efficient dynamic kinetic resolution, involving a crystallization step, have been developed. In particula作者: 抱怨 時(shí)間: 2025-3-28 07:52 作者: 真實(shí)的人 時(shí)間: 2025-3-28 11:43
978-3-662-14612-5Springer-Verlag Berlin Heidelberg 2003作者: 干旱 時(shí)間: 2025-3-28 16:40
Organolithiums in Enantioselective Synthesis978-3-540-36117-6Series ISSN 1436-6002 Series E-ISSN 1616-8534 作者: 破裂 時(shí)間: 2025-3-28 22:07
Enantioselective Synthesis by Lithiation Adjacent to Oxygen and Subsequent Rearrangement,s field is presented. The first section concerns asymmetric Wittig rearrangements. Asymmetric retro-Brook rearrangements are then covered, followed by rearrangements of phosphate to phosphonate. The last section reviews asymmetric rearrangements of lithiated epoxides.作者: Indicative 時(shí)間: 2025-3-29 02:04
Enantioselective Synthesis by Lithiation to Generate Planar or Axial Chirality,laying these stereochemical features are ferrocenes, arenechromium tricarbonyl complexes, biaryls, atropisomeric amides and allenes. Methods for the enantioselective lithiation of these compound classes, relying on either substrate (chiral auxiliary) or reagent (chiral base) control will be reviewed.作者: 厭倦嗎你 時(shí)間: 2025-3-29 06:45
