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302 related items for PubMed ID: 18363375
1. An efficient protocol for the enantioselective preparation of a key polyfunctionalized cyclohexane. New access to (R)- and (S)-4-Hydroxy-2-cyclohexenone and (R)- and (S)-trans-cyclohex-2-ene-1,4-diol. Bayón P, Marjanet G, Toribio G, Alibés R, de March P, Figueredo M, Font J. J Org Chem; 2008 May 02; 73(9):3486-91. PubMed ID: 18363375 [Abstract] [Full Text] [Related]
2. Dioxygenase-catalysed cis-dihydroxylation of meta-substituted phenols to yield cyclohexenone cis-diol and derived enantiopure cis-triol metabolites. Boyd DR, Sharma ND, Stevenson PJ, Blain M, McRoberts C, Hamilton JT, Argudo JM, Mundi H, Kulakov LA, Allen CC. Org Biomol Chem; 2011 Mar 07; 9(5):1479-90. PubMed ID: 21221457 [Abstract] [Full Text] [Related]
6. Resolution of racemic 2-aminocyclohexanol derivatives and their application as ligands in asymmetric catalysis. Schiffers I, Rantanen T, Schmidt F, Bergmans W, Zani L, Bolm C. J Org Chem; 2006 Mar 17; 71(6):2320-31. PubMed ID: 16526780 [Abstract] [Full Text] [Related]
8. Asymmetric synthesis of the epimeric (3S)-3-((E)-hex-1-enyl)-2-methylcyclohexanones. Vrielynck FA, De Clercq PJ. Molecules; 2007 Feb 21; 12(2):237-44. PubMed ID: 17846574 [Abstract] [Full Text] [Related]
9. Alpha-alkenoyl ketene S,S-acetal-based multicomponent reaction: an efficient approach for the selective construction of polyfunctionalized cyclohexanones. Ma Y, Wang M, Li D, Bekturhun B, Liu J, Liu Q. J Org Chem; 2009 Apr 17; 74(8):3116-21. PubMed ID: 19296593 [Abstract] [Full Text] [Related]
11. Chemoenzymatic synthesis of rivastigmine based on lipase-catalyzed processes. Mangas-Sánchez J, Rodríguez-Mata M, Busto E, Gotor-Fernández V, Gotor V. J Org Chem; 2009 Aug 07; 74(15):5304-10. PubMed ID: 19555095 [Abstract] [Full Text] [Related]
12. Practical and efficient multigram preparation of a camphor-derived diol for the enantioselective Lewis acid catalyzed allylboration of aldehydes. Lachance H, St-Onge M, Hall DG. J Org Chem; 2005 May 13; 70(10):4180-3. PubMed ID: 15876115 [Abstract] [Full Text] [Related]
13. Gold-catalyzed tandem C-C and C-O bond formation: a highly diastereoselective formation of cyclohex-4-ene-1,2-diol derivatives. Lim C, Kang JE, Lee JE, Shin S. Org Lett; 2007 Aug 30; 9(18):3539-42. PubMed ID: 17665922 [Abstract] [Full Text] [Related]
14. [Lipase-catalyzed kinetic resolution of 2-substituted cycloalkanols]. Forró E. Acta Pharm Hung; 2001 Aug 30; 71(1):119-26. PubMed ID: 11769092 [Abstract] [Full Text] [Related]
17. Enantiodivergent preparation of optically active oxindoles having a stereogenic quaternary carbon center at the C3 position via the lipase-catalyzed desymmetrization protocol: effective use of 2-furoates for either enzymatic esterification or hydrolysis. Akai S, Tsujino T, Akiyama E, Tanimoto K, Naka T, Kita Y. J Org Chem; 2004 Apr 02; 69(7):2478-86. PubMed ID: 15049648 [Abstract] [Full Text] [Related]
18. New families of enantiopure cyclohexenone cis-diol, o-quinol dimer and hydrate metabolites from dioxygenase-catalysed dihydroxylation of phenols. Boyd DR, Sharma ND, Malone JF, Allen CC. Chem Commun (Camb); 2009 Jun 28; (24):3633-5. PubMed ID: 19521632 [Abstract] [Full Text] [Related]
19. Synthesis of (R)-(+)-4-methylcyclohex-2-ene-1-one. Tun MK, Herzon SB. J Org Chem; 2012 Oct 19; 77(20):9422-5. PubMed ID: 23030397 [Abstract] [Full Text] [Related]
20. A new powerful strategy for the organocatalytic asymmetric construction of a quaternary carbon stereogenic center. Inokoishi Y, Sasakura N, Nakano K, Ichikawa Y, Kotsuki H. Org Lett; 2010 Apr 02; 12(7):1616-9. PubMed ID: 20222687 [Abstract] [Full Text] [Related] Page: [Next] [New Search]