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2-((2S,3R,4S)-6-chloro-1,2,3,4-tetrahydro-3-nitro-2-phenyl-1-tosylquinolin-4-yl)-1-phenylethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1619985-36-2

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1619985-36-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1619985-36-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,9,9,8 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1619985-36:
(9*1)+(8*6)+(7*1)+(6*9)+(5*9)+(4*8)+(3*5)+(2*3)+(1*6)=222
222 % 10 = 2
So 1619985-36-2 is a valid CAS Registry Number.

1619985-36-2Downstream Products

1619985-36-2Relevant academic research and scientific papers

Asymmetric domino aza-Michael-Michael reaction of o-N-protected aminophenyl α,β-unsaturated ketones: Construction of chiral functionalized tetrahydroquinolines

Kim, Shinae,Kang, Ki-Tae,Kim, Sung-Gon

, p. 5114 - 5121 (2014/07/08)

The diastereo- and enantioselective synthesis of 2,3,4-trisubstituted tetrahydroquinolines has been developed through organocatalytic domino aza-Michael-Michael reaction of o-N-tosylaminophenyl α,β-unsaturated ketones with nitroalkenes. This useful and simple domino process afforded diverse highly functionalized tetrahydroquinolines, some of which are not easily accessible using other methodologies, in good yields and with excellent diastereo- and enantioselectivities (up to >30:1 dr, >99% ee).

Asymmetric domino aza-Michael-Michael reaction of o-N-protected aminophenyl α,β-unsaturated ketones: Construction of chiral functionalized tetrahydroquinolines

Kim, Shinae,Kang, Ki-Tae,Kim, Sung-Gon

, p. 5114 - 5121 (2014/12/10)

The diastereo- and enantioselective synthesis of 2,3,4-trisubstituted tetrahydroquinolines has been developed through organocatalytic domino aza-Michael-Michael reaction of o-N-tosylaminophenyl α,β-unsaturated ketones with nitroalkenes. This useful and simple domino process afforded diverse highly functionalized tetrahydroquinolines, some of which are not easily accessible using other methodologies, in good yields and with excellent diastereo- and enantioselectivities (up to >30:1 dr, >99% ee).

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