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(S)-1-(4-methoxyphenyl)but-3-en-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106650-97-9

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106650-97-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106650-97-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,6,5 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 106650-97:
(8*1)+(7*0)+(6*6)+(5*6)+(4*5)+(3*0)+(2*9)+(1*7)=119
119 % 10 = 9
So 106650-97-9 is a valid CAS Registry Number.

106650-97-9Relevant academic research and scientific papers

Asymmetrie allylation of aldehydes catalyzed by simple dual small organic molecules: L-proline and L-prolinol

Chen, Guo-Hong,Liu, Ling-Yan,Wei, Xiao-Ning,Chang, Wei-Xing,Li, Jing

, p. 1013 - 1015 (2010)

A novel and simple methodology for the asymmetric allylation of aldehydes was reported. Double small organic molecules such as L-proline and L-prolinol were first employed for providing a chiral environment so as to afford chiral homoallylic alcohols in high yields and moderate enantioselectivities in our protocol.

The first series of chiral 2,2′:6′,2″-terpyridine tri-N-oxide ligands for Lewis base-catalyzed asymmetric allylation of aldehydes

Wong, Wing-Leung,Lee, Chi-Sing,Leung, Hon-Kit,Kwong, Hoi-Lun

, p. 1967 - 1969 (2004)

The first series of chiral 2,2′:6′2″-terpyridine tri-N-oxide ligands have been developed; They were showed to be active Lewis base-catalysts for asymmetric allylation of aldehydes using allyltrichlorosilane with optimal results at 0°C for electron-deficie

A highly enantioselective indium-mediated allylation reaction of aldehydes

Loh, Teck-Peng,Zhou, Jian-Rong,Yin, Zheng

, p. 1855 - 1857 (1999)

(formula presented) The first highly enantioselective indium-mediated allylation of aldehydes was reported. In most cases, good chemical yields and moderate to high enantioselectivies (up to 90% ee) were obtained in the presence of external chiral ligands

Synthesis of helical π-conjugated polymers bearing pyridine: N -oxide pendants and asymmetric allylation of aldehydes in the helical cavity

Ikai, Tomoyuki,Yoshida, Takumu

, p. 8537 - 8540 (2019)

Catalytically active chiral π-conjugated polymers (poly-1(NO)r) bearing pyridine N-oxide pendants were synthesized by ternary copolymerization of a d-glucose-bound diethynyl compound with two types of thieno[3,4-b]thiophene comonomer, one of wh

Chiral bis(oxazolinyl)phenylrhodium(III) complexes as Lewis acid catalysts for enantioselective allylation of aldehydes

Motoyama, Yukihiro,Narusawa, Hiroki,Nishiyama, Hisao

, p. 131 - 132 (1999)

The reaction of (Phebox)SnMe3 1 [PheboxH = 2,6-bis(oxazolinyl)benzene] and [(c-octene)RhCl]2 in the presence of CCl4 provided air-stable and water-tolerant (Phebox)RhCl2(H2O) complexes 2 which acted a

Asymmetric allylation reactions of achiral aldehydes with diallyltin dibromide by the use of chiral diamines

Kobayashi, Shu

, p. 6729 - 6732 (1995)

Asymmetric allylation reactions of achiral aldehydes with diallyltin dibromide have been achieved by using a chiral diamine derived from L-proline as a promoter.

Biocatalytic Dynamic Kinetic Resolution for the Synthesis of Atropisomeric Biaryl N-Oxide Lewis Base Catalysts

Staniland, Samantha,Adams, Ralph W.,McDouall, Joseph J. W.,Maffucci, Irene,Contini, Alessandro,Grainger, Damian M.,Turner, Nicholas J.,Clayden, Jonathan

, p. 10755 - 10759 (2016)

Atropisomeric biaryl pyridine and isoquinoline N-oxides were synthesized enantioselectively by dynamic kinetic resolution (DKR) of rapidly racemizing precursors exhibiting free bond rotation. The DKR was achieved by ketoreductase (KRED) catalyzed reductio

Isotope effects and heavy-atom tunneling in the Roush allylboration of aldehydes

Vetticatt, Mathew J.,Singleton, Daniel A.

, p. 2370 - 2373 (2012)

Intermolecular 13C kinetic isotope effects (KIEs) for the Roush allylboration of p-anisaldehyde were determined using a novel approach. The experimental 13C KIEs fit qualitatively with the expected rate-limiting cyclic transition sta

A highly practical and enantioselective reagent for the allylation of aldehydes

Kubota, Katsumi,Leighton, James L.

, p. 946 - 948 (2003)

Strain at silicon is the key to success of reagent 1 since this strain, which is induced by the diazasilacyclopentane ring, determines its reactivity. This practical and general new reagent for the highly enantioselective allylation of aldehydes is easily prepared as an air-stable solid and may be stored without significant decomposition.

Chiral bipyridine-annulated bicyclo[3.3.1]nonane N-oxide organocatalysts for stereoselective allylation and hydrosilylation reactions

?eimyt?, Simona,Ston?ius, Sigitas

supporting information, (2020/12/21)

The synthesis of chiral C2-symmetric bis(bipyridine N,N′-dioxide) and bis(bipyridine N-monooxide) derivatives featuring bipyridine-annulated bicyclo[3.3.1]nonane framework is reported. The new Lewis basic bipyridine N,N′-dioxides exhibited good

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