PEL
发表于 2025-3-21 17:56:48
书目名称Organolithiums in Enantioselective Synthesis影响因子(影响力)<br> http://figure.impactfactor.cn/if/?ISSN=BK0704498<br><br> <br><br>书目名称Organolithiums in Enantioselective Synthesis影响因子(影响力)学科排名<br> http://figure.impactfactor.cn/ifr/?ISSN=BK0704498<br><br> <br><br>书目名称Organolithiums in Enantioselective Synthesis网络公开度<br> http://figure.impactfactor.cn/at/?ISSN=BK0704498<br><br> <br><br>书目名称Organolithiums in Enantioselective Synthesis网络公开度学科排名<br> http://figure.impactfactor.cn/atr/?ISSN=BK0704498<br><br> <br><br>书目名称Organolithiums in Enantioselective Synthesis被引频次<br> http://figure.impactfactor.cn/tc/?ISSN=BK0704498<br><br> <br><br>书目名称Organolithiums in Enantioselective Synthesis被引频次学科排名<br> http://figure.impactfactor.cn/tcr/?ISSN=BK0704498<br><br> <br><br>书目名称Organolithiums in Enantioselective Synthesis年度引用<br> http://figure.impactfactor.cn/ii/?ISSN=BK0704498<br><br> <br><br>书目名称Organolithiums in Enantioselective Synthesis年度引用学科排名<br> http://figure.impactfactor.cn/iir/?ISSN=BK0704498<br><br> <br><br>书目名称Organolithiums in Enantioselective Synthesis读者反馈<br> http://figure.impactfactor.cn/5y/?ISSN=BK0704498<br><br> <br><br>书目名称Organolithiums in Enantioselective Synthesis读者反馈学科排名<br> http://figure.impactfactor.cn/5yr/?ISSN=BK0704498<br><br> <br><br>
系列
发表于 2025-3-21 21:06:51
http://reply.papertrans.cn/71/7045/704498/704498_2.png
lanugo
发表于 2025-3-22 03:35:08
http://reply.papertrans.cn/71/7045/704498/704498_3.png
ADOPT
发表于 2025-3-22 07:30:48
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.
crescendo
发表于 2025-3-22 09:31:28
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..
DUST
发表于 2025-3-22 14:51:02
http://reply.papertrans.cn/71/7045/704498/704498_6.png
衣服
发表于 2025-3-22 17:06:59
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.
忘恩负义的人
发表于 2025-3-23 01:11:35
http://reply.papertrans.cn/71/7045/704498/704498_8.png
QUAIL
发表于 2025-3-23 02:20:44
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
Myosin
发表于 2025-3-23 07:11:12
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