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18621-06-2

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18621-06-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18621-06-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,6,2 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 18621-06:
(7*1)+(6*8)+(5*6)+(4*2)+(3*1)+(2*0)+(1*6)=102
102 % 10 = 2
So 18621-06-2 is a valid CAS Registry Number.

18621-06-2Relevant academic research and scientific papers

Hydrogen-Borrowing Alkylation of 1,2-Amino Alcohols in the Synthesis of Enantioenriched γ-Aminobutyric Acids

Hall, Christopher J. J.,Goundry, William R. F.,Donohoe, Timothy J.

supporting information, p. 6981 - 6985 (2021/03/01)

For the first time we have been able to employ enantiopure 1,2-amino alcohols derived from abundant amino acids in C?C bond-forming hydrogen-borrowing alkylation reactions. These reactions are facilitated by the use of the aryl ketone Ph*COMe. Racemisation of the amine stereocentre during alkylation can be prevented by the use of sub-stoichiometric base and protection of the nitrogen with a sterically hindered triphenylmethane (trityl) or benzyl group. The Ph* and trityl groups are readily cleaved in one pot to give γ-aminobutyric acid (GABA) products as their HCl salts without further purification. Both steps may be performed in sequence without isolation of the hydrogen-borrowing intermediate, removing the need for column chromatography.

The synthetic and biological studies of discorhabdins and related compounds

Wada, Yasufumi,Harayama, Yu,Kamimura, Daigo,Yoshida, Masako,Shibata, Tomoyuki,Fujiwara, Kousaku,Morimoto, Koji,Fujioka, Hiromichi,Kita, Yasuyuki

scheme or table, p. 4959 - 4976 (2011/08/06)

Various analogues of the marine alkaloids, discorhabdins, have been synthesized. The strategy contains spirocyclization with phenyliodine(iii) bis(trifluoroacetate) (PIFA), oxidative fragmentation of the β-amino alcohols with the hypervalent iodine reagent C6F 5I(OCOCF3)2, the detosylation and dehydrogenation reaction of the pyrroloiminoquinone unit in the presence of a catalytic amount of NaN3 and the bridged ether synthesis with HBr-AcOH as the key reactions. All the synthesized compounds were evaluated by in vitro MTT assay for cytotoxic activity against the human colon cancer cell line HCT-116. Furthermore, the discorhabdin A oxa analogues were also evaluated against four kinds of tumor model cells, a human colon cancer cell line (WiDr), a human prostate cancer cell line (DU-145) and murine leukemia cell lines (P388 and L1210). For the identification of the target, discorhabdin A and the discorhabdin A oxa analogue were evaluated by an HCC panel assay. In the test, discorhabdins could have a novel mode of action with the tumor cells. The Royal Society of Chemistry 2011.

The first total synthesis of discorhabdin A

Tohma, Hirofumi,Harayama, Yu,Hashizume, Miki,Iwata, Minako,Kiyono, Yorito,Egi, Masahiro,Kita, Yasuyuki

, p. 11235 - 11240 (2007/10/03)

The first stereoselective total synthesis of a potent antitumor alkaloid, discorhabdin A (1), which is a unique sulfur-containing pyrroloiminoquinone alkaloid, is described. The key step in the stereocontrolled total synthesis of 1 involves both a diaster

Synthetic studies on the sulfur-cross-linked core of antitumor marine alkaloid, discorhabdins: Total synthesis of discorhabdin A

Tohma, Hirofumi,Harayama, Yuu,Hashizume, Miki,Iwata, Minako,Egi, Masahiro,Kita, Yasuyuki

, p. 348 - 350 (2007/10/03)

A concise and efficient method to construct the characteristic sulfur-cross-linked core of an unprecedented antitumor marine alkaloid, discorhabdins, has been developed. By utilizing this methodology the first total synthesis of (±)-discorhabdin A (1) has

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