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N-benzyloxycarbonyl-2-allylaniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86136-89-2

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86136-89-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86136-89-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,1,3 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 86136-89:
(7*8)+(6*6)+(5*1)+(4*3)+(3*6)+(2*8)+(1*9)=152
152 % 10 = 2
So 86136-89-2 is a valid CAS Registry Number.

86136-89-2Relevant academic research and scientific papers

M-CPBA-Mediated Intramolecular Aminohydroxylation of N-Sulfonyl Aminoalkenes to Synthesize β-Hydroxyl Cyclic Amines

Yin, Yan,Zhou, Hong,Sun, Guofeng,Liu, Xichen

, p. 1337 - 1345 (2015/10/06)

A variety of structurally diverse N-sulfonyl-protected aminoalkenes readily reacted with m-CPBA to produce a series of β-hydroxyl cyclic amines in high yields through intramolecular aminohydroxylation. This metal-free and easy-to-handle synthetic methodol

Asymmetric indoline synthesis via intramolecular aza-Michael addition mediated by bifunctional organocatalysts

Miyaji, Ryota,Asano, Keisuke,Matsubara, Seijiro

, p. 3658 - 3661 (2013/08/23)

A novel method for the asymmetric synthesis of 2-substituted indolines, employing bifunctional amino(thio)urea catalysts, was developed. The reaction proceeded via an intramolecular aza-Michael addition mediated by activation through hydrogen bonding. The

Organocatalytic approach to benzofused nitrogen-containing heterocycles: Enantioselective total synthesis of (+)-angustureine

Fustero, Santos,Moscardo, Javier,Jimenez, Diego,Perez-Carrion, Maria Dolores,Sanchez-Rosello, Maria,Del Pozo, Carlos

supporting information; experimental part, p. 9868 - 9872 (2009/10/20)

A study was conducted to demonstrate an organocatalytic approach to benzofused nitrogen-containing heterocycles. he study also demonstrated enantioselective total synthesis of (+)-angustureine. It reported the easy an d enantioselective preparation of tet

Improved protocol for asymmetric, intramolecular heteroatom Michael addition using organocatalysis: Enantioselective syntheses of homoproline, pelletierine, and homopipecolic acid

Carlson, Erik C.,Rathbone, Lauren K.,Yang, Hua,Collett, Nathan D.,Carter, Rich G.

, p. 5155 - 5158 (2008/09/21)

(Chemical Equation Presented) An improved protocol for the construction of enantioenriched pyrrolidine, indoline, and piperidine rings using an organocatalyzed, intramolecular heteroatom Michael addition is described. Application to the enantioselective synthesis of homoproline, homopipecolic acid, and pelletierine has been accomplished.

Gold(I)-catalyzed intramolecular hydroamination of alkenyl carbamates

Han, Xiaoqing,Widenhoefer, Ross A.

, p. 1747 - 1749 (2007/10/03)

(Chemical Equation Presented) Gold for rings: Reaction of alkenyl carbamates such as 1 in the presence of [Au{P(tBu)2(o-biphenyl)}]Cl and AgOTf led to nitrogen heterocycles (e.g. 2). This AuI-catalyzed intramolecular hydroamination t

Construction of nitrogen-heterocyclic compounds through zirconium mediated intramolecular alkene-carbonyl coupling reaction of N-(o-alkenylaryl)carbamate derivatives

Takigawa, Yasushi,Ito, Hisanaka,Omodera, Katsunori,Ito, Maiko,Taguchi, Takeo

, p. 1385 - 1392 (2007/10/03)

Intramolecular alkene-carbonyl coupling reaction of N-benzyl-N-(o- alkenylaryl)carbamate derivative derived from o-aminostyrene, o-(aminomethyl)styrene and o-aminoallylbenzene smoothly proceeded by treating with zirconocene-butene complex to give the corresponding lactam derivative.

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