ライフサイエンスコーパス: butyllithium

1 ixed aggregate and a 2:1 mixed trimer with n-butyllithium.

2 itu of an aryne species in the presence of n-butyllithium.

3 -(tert-butyloxycarbonyl)pyrrolidine with sec-butyllithium.

4 tly a 2:2 ladder-type mixed aggregate with n-butyllithium.

5 In the methyllithium and n-butyllithium addition to 4[symbol: see text]1 and 4[symb

6 onium salt 1c, which upon deprotonation with butyllithium affords the corresponding stable C-amino ph

7 A 2:1 lithium amide/ n-butyllithium aggregate 1 is investigated as an asymmetri

8 Treatment of 2- and 3-thienyloxazolines with butyllithium and bis(trimethylsilyl) peroxide results in

9 etween p-(LiC2)2C6H4 (generated in situ from butyllithium and dialkynylbenzene) and 2 equiv of BPh3 a

10 reacting protected bromobenzaldehydes with n-butyllithium and ethyl N,N-dimethylcarbamate.

11 The highly basic reagents sec-butyllithium and tert-butyllithium can be titrated in et

12 sopropylaminoborohydride are prepared from n-butyllithium and the corresponding amine-borane.

13 opylphenyl), can be prepared from H2[Ar2N3], butyllithium, and (t-BuO)3Mo(N).

14 -((triisopropylsilyl)oxy)butan-2-amine and n-butyllithium are characterized by various NMR experiment

15 alkylcuprates prepared from high-quality sec-butyllithium are thermally stable for 2-3 h at room temp

16 synthesis of alpha-Mn nanoparticles using n-butyllithium as a reducing agent.

17 ic compounds Au3Fe, Au3Co, and Au3Ni using n-butyllithium as a reducing agent.

18 metric induction in the presence of excess n-butyllithium can be obtained.

19 hly basic reagents sec-butyllithium and tert-butyllithium can be titrated in ether solution, where th

20 ere synthesized via reduction of SiI4 with n-butyllithium, capped with octanol and precipitated from

21 n at the benzylic position with a mixture of butyllithium/diisopropylamine/potassium t-butoxide and p

22 Crystallography shows a trilithiated n-butyllithium-dilithiated amide that has dimerized to a h

23 s subjected to halogen-lithium exchange with butyllithium, followed by carbonation with CO2 or formyl

24 romo-3,6-diarylbenzenes in the presence of n-butyllithium, followed by deoxygenation of the double ad

25 reatment of 4-organoselenylisoxazoles with n-butyllithium, followed by trapping with electrophiles, f

26 yl)ethyl)-N,N-dimethylurea with 3 equiv of n-butyllithium in anhydrous THF at 0 degrees C takes place

27 r N-isopropyl alaninol were lithiated with n-butyllithium in tetrahydrofuran or diethyl ether.

28 at methyl by LiN(CH2CH2OCH3)3 as well as by butyllithium in the presence of PMDTA producing isoprope

29 eNCO2Me)NHCH(Me)Ph (5; dr of 95:5) with tert-butyllithium in THF has been elucidated using multinucle

30 When it was reacted with n-butyllithium, intermediate 1 once again surprisingly gen

31 ures of the mixed aggregates of n-butyl, sec-butyllithium, isopropyllithium with lithiated (S)-N-ethy

32 further improved in the presence of a LiTMP-butyllithium mixed aggregate.

33 borane [(iPr)(2)N:BH(3)] with 1.1 equiv of n-butyllithium (n-BuLi) followed by methyl iodide (MeI), o

34 n-Butyllithium/N,N,N',N'-tetramethylethylenediamine-mediat

35 om the corresponding tributylstannanes and n-butyllithium or by deprotonation of N-(tert-butyloxycarb

36 n reactions can succeed with low-quality sec-butyllithium, presumably containing insoluble lithium hy

37 Treatment of 5a with excess butyllithium provided the acetylenic derivative 9-(5,6,

38 CuCN, CuCN.2LiCl, CuI), cuprate reagent, sec-butyllithium quality, solvent, and temperature upon the

39 -Pr)C(Me)N(i-Pr)]Cl(2) (3) with 2 equiv of n-butyllithium, revealed a smaller d(NN) value of 1.189(4)

40 The anionic polymerization of 2 with sec-butyllithium (s-BuLi) in cyclohexane gave poly-2 in quan

41 rcinols after treatment with 4 equiv of tert-butyllithium similarly afforded 2-(alkyltelluro)resorcin

42 ure of the corresponding bromoalkenes with n-butyllithium succeeded by means of a user-friendly (E)-1

43 Upon treatment with n-butyllithium, the open analogue exhibits Bronsted base c

44 ted-state deprotonation of dixanthene with n-butyllithium/TMEDA resulted in formation of the tetraani

45 zaallyl)stannanes may be transmetalated by n-butyllithium to generate 2-azaallyllithiums, which also

46 cols with unpurified commercial samples of n-butyllithium to prepare LDA or commercially available LD

47 on of 2,6-dibromophenol with 5 equiv of tert-butyllithium to react with dialkyl ditellurides.

48 duced from 2-bromophenol and 3 equiv of tert-butyllithium was allowed to react with dialkyl ditelluri