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343871-08-9

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343871-08-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 343871-08-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,3,8,7 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 343871-08:
(8*3)+(7*4)+(6*3)+(5*8)+(4*7)+(3*1)+(2*0)+(1*8)=149
149 % 10 = 9
So 343871-08-9 is a valid CAS Registry Number.

343871-08-9Relevant academic research and scientific papers

An Industrial Perspective on Counter Anions in Gold Catalysis: Underestimated with Respect to “Ligand Effects”

Schie?l, Jasmin,Schulmeister, Jürgen,Doppiu, Angelino,W?rner, Eileen,Rudolph, Matthias,Karch, Ralf,Hashmi, A. Stephen K.

, p. 2493 - 2502 (2018)

The conversion of a variety of well-known test reactions, representing the key reactivity patterns of gold catalysis, were analyzed by GC and 1H NMR. The study is focused on establishing of a strategical approach for the consideration of ligand

Complex Polyheterocycles and the Stereochemical Reassignment of Pileamartine A via Aza-Heck Triggered Aryl C-H Functionalization Cascades

Bower, John F.,Caiger, Lewis,García-Cárceles, Javier,Hazelden, Ian R.,Jones, Benjamin T.,Langer, Thomas,Lewis, Richard J.

, p. 15593 - 15598 (2021/10/12)

Structurally complex benzo- and spiro-fused N-polyheterocycles can be accessed via intramolecular Pd(0)-catalyzed alkene 1,2-aminoarylation reactions. The method uses N-(pentafluorobenzoyloxy)carbamates as the initiating motif, and this allows aza-Heck-type alkene amino-palladation in advance of C-H palladation of the aromatic component. The chemistry is showcased in the first total synthesis of the complex alkaloid (+)-pileamartine A, which has resulted in the reassignment of its absolute stereochemistry.

An Industrial Perspective on Counter Anions in Gold Catalysis: On Alternative Counter Anions

Schie?l, Jasmin,Schulmeister, Jürgen,Doppiu, Angelino,W?rner, Eileen,Rudolph, Matthias,Karch, Ralf,Hashmi, A. Stephen K.

, p. 3949 - 3959 (2018/09/06)

A comparison of versatile counter anions was investigated by means of a variety of well-known test reactions representing the key reactivity patterns of homogeneous gold catalysis, the catalytic activity was monitored by GC and 1H NMR. As previ

The bioinspired design of a reagent allows the functionalization of Cα-H of α,β-unsaturated carbonyl compounds via the Baylis-Hillman chemistry under ambient conditions

Singh, Palwinder,Kumar, Arun,Kaur, Sukhmeet,Kaur, Jagroop,Singh, Harpreet

supporting information, p. 2936 - 2939 (2016/02/20)

A rationally designed reagent capable of affecting alkylation at Cα of α,β-unsaturated carbonyl compounds is reported. The reaction proceeded at room temperature without any additives. The pH and H-bond formation during the reaction play a key role in the working of the reagent.

METHOD FOR THE PREPARATION OF alpha-SUBSTITUTED ACRYL ALDEHYDES

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Paragraph 0119, (2016/04/19)

The invention discloses simple and rapid method for the preparation of α-substituted acryl aldehydes. More particularly, the invention discloses a method for the preparation of α-substituted acryl aldehydes via a gold-catalysed [1,3] rearrangement of the allenyl ethers with a record turnover frequency of 4600 h?1 at 0.05 mol % of the catalyst concentration in homogeneous gold(I) catalysis. The α-substituted acryl aldehydes synthesized by the instant process are used as building blocks in organic synthesis.

Gold(i)-catalysed [1,3] O→C rearrangement of allenyl ethers

Kona, Chandrababu Naidu,Ramana, Chepuri V.

supporting information, p. 2152 - 2154 (2014/02/14)

A simple and rapid access to the α-substituted acryl aldehydes has been provided by developing a gold-catalysed [1,3] rearrangement of the allenyl ethers importantly with a record turnover frequency of 4600 h-1 (at 0.05 mol% of the catalyst concentration) in homogeneous gold(i) catalysis. The Royal Society of Chemistry.

Chiral primary amine catalyzed asymmetric epoxidation of α-substituted acroleins

Li, Jiuyuan,Fu, Niankai,Zhang, Long,Zhou, Pengxin,Luo, Sanzhong,Cheng, Jin-Pei

supporting information; experimental part, p. 6840 - 6849 (2011/03/19)

1,1-Disubstituted terminal alkenes remain challenging substrates in asymmetric epoxidation reactions. In this study, chiral primary amines are shown to catalyze the asymmetric epoxidation of α-substituted acroleins, a versatile type of 1,1-disubstituted t

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