27098-65-3Relevant articles and documents
Directed addition of sulfur-stabilised carbanions to 1,2,3-trisubstituted aziridines
Craig, Donald,Lu, Pengfei,Mathie, Tanya,Tholen, Niels T.H.
, p. 6376 - 6382 (2010)
Thioether and sulfone-stabilised carbanions possessing varying functional groups enter into highly regioselective, stereospecific ring-opening reactions with vinyl- and hydroxymethyl-substituted aziridines. Some derivatisation reactions of the adducts are
Enantioselective Synthesis of (?)-Halenaquinone
Goswami, Subir,Harada, Kenichi,El-Mansy, Mohamed F.,Lingampally, Rajinikanth,Carter, Rich G.
supporting information, p. 9117 - 9121 (2018/07/24)
The efficient, 12–14 step (LLS) total synthesis of (?)-halenaquinone has been achieved. Key steps in the synthetic sequence include: (a) proline sulfonamide-catalyzed, Yamada–Otani reaction to establish the C6 all-carbon quaternary stereocenter, (b) multi
HERBICIDE COMPOSITION
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Paragraph 0481-0484, (2015/11/03)
There is provided a herbicidal composition containing a cyclohexanone compound represented by Formula (I) and at least one compound selected from Group A. Group A: consisting of benoxacor, cloquintocet-mexyl, cyometrinil, dichlormid, fenchlorazole-ethyl,