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163399-75-5

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163399-75-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 163399-75-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,3,9 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 163399-75:
(8*1)+(7*6)+(6*3)+(5*3)+(4*9)+(3*9)+(2*7)+(1*5)=165
165 % 10 = 5
So 163399-75-5 is a valid CAS Registry Number.

163399-75-5Downstream Products

163399-75-5Relevant academic research and scientific papers

Synergistic Pd/Amine-Catalyzed Stereodivergent Hydroalkylation of 1,3-Dienes with Aldehydes: Reaction Development, Mechanism, and Stereochemical Origins

Wang, Hongfa,Zhang, Qinglong,Zhang, Ruiyuan,Zi, Weiwei

supporting information, p. 10948 - 10962 (2021/08/03)

Metal-hydride-catalyzed hydroalkylation of 1,3-dienes with enolizable carbonyl compounds is an atom- and step-economical method for preparing chiral molecules with allylic stereocenters. Although high diastereo- and enantioselectivities have been achieved

Determination of the absolute configurations and total synthesis of new immunosuppressants, mycestericins E and G

Fujita, Tetsuro,Hamamichi, Norimitsu,Matsuzaki, Tohru,Kitao, Yuki,Kiuchi, Masatoshi,Node, Manabu,Hirose, Ryoji

, p. 8599 - 8602 (2007/10/02)

The absolute configurations of two new immunosuppressant, mycestericins E (1) and G (2), were established and both compounds were synthesized starting from 1,8-octanediol and a fully protected methyl (2S,4R)-oxazolidine-4-carboxylate 3. Compounds 5 and 22

Asymmetric Total Synthesis of ISP-I (Myriocin, Thermozymocidin), a Potent Immunosuppressive Principle in the Isaria sinclairii Metabolite

Shigeki, Sano,Kobayashi, Yoshimaro,Kondo, Tatsuya,Takebayashi, Maki,Maruyama, Shigeki,et al.

, p. 2097 - 2100 (2007/10/02)

Asymmetric total synthesis of ISP-I has been achived by utilizing highly selectrive E-olefin formation based on the Schlosser-modified Wittig reaction and highly diastereoselective aldol reactions employing both chiral heterocyclic derivatives, 3-acetyl-(4S)-isopropyl-1,3-thiazolidine-2-thione and ethyl -2-yl carboxylate.

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