These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
8. Stereoselective synthesis of trans-fused 7,6,6,7-membered tetracyclic ether, corresponding to the EFGH-ring of gambierol and the BCDE-ring of gambieric acids. Saito T, Nakata T. Org Lett; 2009 Jan 01; 11(1):113-6. PubMed ID: 19053801 [Abstract] [Full Text] [Related]
10. [Development of radical reactions in water aimed at environmentally benign synthetic reactions]. Ueda M. Yakugaku Zasshi; 2004 Jun 01; 124(6):311-9. PubMed ID: 15170066 [Abstract] [Full Text] [Related]
11. Carbon-carbon bond formation and pyrrole synthesis via the [3,3] sigmatropic rearrangement of O-vinyl oxime ethers. Wang HY, Mueller DS, Sachwani RM, Londino HN, Anderson LL. Org Lett; 2010 May 21; 12(10):2290-3. PubMed ID: 20411970 [Abstract] [Full Text] [Related]
12. Short and stereoselective total synthesis of furano lignans (+/-)-dihydrosesamin, (+/-)-lariciresinol dimethyl ether, (+/-)-acuminatin methyl ether, (+/-)-sanshodiol methyl ether, (+/-)-lariciresinol, (+/-)-acuminatin, and (+/-)-lariciresinol monomethyl ether and furofuran lignans (+/-)-sesamin, (+/-)-eudesmin, (+/-)-piperitol methyl ether, (+/-)-pinoresinol, (+/-)-piperitol, and (+/-)-pinoresinol monomethyl ether by radical cyclization of epoxides using a transition-metal radical source. Roy SC, Rana KK, Guin C. J Org Chem; 2002 May 17; 67(10):3242-8. PubMed ID: 12003531 [Abstract] [Full Text] [Related]
13. Enantioselective radical cyclizations: a new approach to stereocontrol of cascade reactions. Miyabe H, Takemoto Y. Chemistry; 2007 May 17; 13(26):7280-6. PubMed ID: 17659664 [Abstract] [Full Text] [Related]
14. Radical addition-initiated domino reactions of conjugated oxime ethers. Ueda M. Chem Pharm Bull (Tokyo); 2014 May 17; 62(9):845-55. PubMed ID: 25177013 [Abstract] [Full Text] [Related]
16. Heck-type cyclization of oxime ethers: stereoselective carbon-carbon bond formation with aryl halides to produce heterocyclic oximes. Ohno H, Aso A, Kadoh Y, Fujii N, Tanaka T. Angew Chem Int Ed Engl; 2007 May 17; 46(33):6325-8. PubMed ID: 17640020 [No Abstract] [Full Text] [Related]
17. Acetylenic bond participation in biogenetic-like olefinic cyclizations in nitroalkane solvents. Synthesis of the 17-hydroxy-5 beta-pregnan-20-one system. Morton DR, Gravestock MB, Parry RJ, Johnson WS. J Am Chem Soc; 1973 Jun 27; 95(13):4417-8. PubMed ID: 4708389 [No Abstract] [Full Text] [Related]
18. A convergent coupling strategy for the formation of polycyclic ethers: stereoselective synthesis of the BCDE fragment of brevetoxin A. Crimmins MT, McDougall PJ, Emmitte KA. Org Lett; 2005 Sep 01; 7(18):4033-6. PubMed ID: 16119960 [Abstract] [Full Text] [Related]
19. Head-to-tail oxime cyclization of oligodeoxynucleotides for the efficient synthesis of circular DNA analogues. Edupuganti OP, Defrancq E, Dumy P. J Org Chem; 2003 Oct 31; 68(22):8708-10. PubMed ID: 14575507 [Abstract] [Full Text] [Related]