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59540-81-7

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59540-81-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59540-81-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,5,4 and 0 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 59540-81:
(7*5)+(6*9)+(5*5)+(4*4)+(3*0)+(2*8)+(1*1)=147
147 % 10 = 7
So 59540-81-7 is a valid CAS Registry Number.

59540-81-7Relevant academic research and scientific papers

Palladium-catalyzed site-selective arylation of aliphatic ketones enabled by a transient ligand

Pan, Lei,Yang, Ke,Li, Guigen,Ge, Haibo

supporting information, p. 2759 - 2762 (2018/03/21)

Transition metal-catalyzed direct C-H bond functionalization enabled by transient ligands has become an attractive topic. Here we report a palladium-catalyzed site-selective arylation of β-C(sp3)-H bonds in aliphatic ketones with β-alanine as the transient ligand.

Design of chiral sulfoxide-olefins as a new class of sulfur-based olefin ligands for asymmetric catalysis

Qi, Wei-Yi,Zhu, Ting-Shun,Xu, Ming-Hua

supporting information; experimental part, p. 3410 - 3413 (2011/08/22)

The design and development of a novel class of chiral sulfur-olefin hybrid ligands with high synthetic feasibility are described. These new sulfoxide-olefin ligands showed excellent catalytic activities and enantioselectivities (up to 98% ee) in rhodium-catalyzed asymmetric 1,4-addition reactions of aryl boronic acids to α,β-unsaturated carbonyl compounds.

Synthesis of β-aryl ketones by tetraphosphine/palladium catalysed Heck reactions of 2- or 3-substituted allylic alcohols with aryl bromides

Berthiol, Florian,Doucet, Henri,Santelli, Maurice

, p. 4372 - 4383 (2007/10/03)

Through the use of [PdCl(C3H5)]2/cis,cis,cis-1,2,3,4-tetrakis(diphenylphosphinomethyl)cyclopentane as a catalyst, a range of aryl bromides undergoes Heck reaction using 2- or 3-subtituted allylic alcohols. With these sterically congested alkenes, the selective formation of β-aryl ketones was observed when appropriate reaction conditions were used. The influence of the functional group on the aryl bromide and of the base on the selectivity is remarkable. With several substrates, much higher selectivities were obtained using NaHCO3 instead of K2CO3 as base. Furthermore, this catalyst can be used at low loading with several substrates.

SYNTHESIS OF JUVABIONE ANALOGUES

Mane, Ramchandra B.,Desai, Uday V.,Hebbalkar, Geeta D.

, p. 646 - 657 (2007/10/02)

Alkylation of various β-ketoesters IIIa-d with bis(p-methoxycarbonylphenyl)bromomethane (II) and bis(p-chlorophenyl)bromomethane (VI) followed by cleavage of ethoxycarbonyl group or hydrolysis and esterification gave methoxycarbonylphenyl and chlorophenyl analogues of ar-juvabione, respectively.Condensation of bis(p-methoxycarbonylphenyl)methanol (IX) with isovaleryl and trichloroacetyl chloride gave isovalerate X and trichloroacetate XI, respectively, while the condensation of bis(p-chlorophenyl)methanol (XII) with isovaleryl chloride and citronellyl bromide yieldedisovalerate XIII and citronellyl ether XIV, respectively.The methoxycarbonylation of aryl-alkyl ketones XVa-d with oxalyl chloride and treatment with methanol furnished various ar-juvabione analogues XVIa-d.The compounds Vb, Vc, Vd, XVIb, and XVIc showed high activity against Dysdercus koenigii at 1μg concentration.

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