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(1S)-2-([tert-butyl(dimethyl)silyl]oxyimino)-1-methylethyl (3S)-3-[(4-methoxybenzyl)oxy] butanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

861903-07-3

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861903-07-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 861903-07-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,1,9,0 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 861903-07:
(8*8)+(7*6)+(6*1)+(5*9)+(4*0)+(3*3)+(2*0)+(1*7)=173
173 % 10 = 3
So 861903-07-3 is a valid CAS Registry Number.

861903-07-3Downstream Products

861903-07-3Relevant articles and documents

Synthetic studies on bioactive natural polyketides: Intramolecular nitrile oxide-olefin cycloaddition approach for construction of a macrolactone skeleton of macrosphelide B

Paek, Seung-Mann,Suh, Young-Ger

, p. 4850 - 4860 (2011/09/12)

Studies on the synthesis of macrosphelide B via an intramolecular nitrile oxideolefin cycloaddition (INOC) is described. In particular, an asymmetric INOC approach using phase transfer catalysts seems to be a potentially efficient and versatile procedure

Concise syntheses of (+)-macrosphelides A and B: Studies on the macro-ring closure strategy

Paek, Seung-Mann,Yun, Hwayoung,Kim, Nam-Jung,Jung, Jong-Wha,Chang, Dong-Jo,Lee, Sujin,Yoo, Jakyung,Park, Hyun-Ju,Suh, Young-Ger

supporting information; experimental part, p. 554 - 561 (2009/07/25)

Highly concise syntheses of (+)-macrosphelides A and B were accomplished in this study. The key feature of our synthetic route involved the direct three-carbon homologation of the readily available Weinreb amide 6 by the addition of a trans-vinylogous est

Concise syntheses of (+)-macrosphelides A and B

Paek, Seung-Mann,Seo, Seung-Yong,Kim, Seok-Ho,Jung, Jong-Wha,Lee, Yong-Sil,Jung, Jae-Kyung,Suh, Young-Ger

, p. 3159 - 3162 (2007/10/03)

(Chemical Equation Presented) Unified and highly convergent total syntheses of (+)-macrosphelides A and B are described. Key features of the syntheses include (1) concise synthesis of the optically active δ-hydroxy-γ- keto α,β-unsaturated acid fragment vi

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