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.
2. Diastereoselective synthesis of the C(17)-C(28) fragment (the C-D spiroketal unit) of spongistatin 1 (altohyrtin A) via a kinetically controlled iodo-spiroketalization reaction. Holson EB; Roush WR Org Lett; 2002 Oct; 4(21):3719-22. PubMed ID: 12375927 [TBL] [Abstract][Full Text] [Related]
3. Synthesis of the C(2)-C(13) fragment (the A-B spiroketal unit) of spongistatin 1 (altohyrtin A): use of a common intermediate for the synthesis of both spongistatin spiroketals. Holson EB; Roush WR Org Lett; 2002 Oct; 4(21):3723-5. PubMed ID: 12375928 [TBL] [Abstract][Full Text] [Related]
4. Synthesis of the C29-C44 portion of spongistatin 1 (altohyrtin A). Wallace GA; Scott RW; Heathcock CH J Org Chem; 2000 Jun; 65(13):4145-52. PubMed ID: 10866633 [TBL] [Abstract][Full Text] [Related]
5. Asymmetric total synthesis of spongistatins 1 and 2. Crimmins MT; Katz JD; Washburn DG; Allwein SP; McAtee LF J Am Chem Soc; 2002 May; 124(20):5661-3. PubMed ID: 12010038 [TBL] [Abstract][Full Text] [Related]
6. Structure-based design of a novel synthetic spiroketal pyran as a pharmacophore for the marine natural product spongistatin 1. Uckun FM; Mao C; Vassilev AO; Huang H; Jan ST Bioorg Med Chem Lett; 2000 Mar; 10(6):541-5. PubMed ID: 10741549 [TBL] [Abstract][Full Text] [Related]
7. An aldol approach to the synthesis of the EF fragment of spongistatin 1. Crimmins MT; Katz JD; McAtee LC; Tabet EA; Kirincich SJ Org Lett; 2001 Mar; 3(6):949-52. PubMed ID: 11263923 [TBL] [Abstract][Full Text] [Related]
8. A modular approach to marine macrolide construction. 3. Enantioselective synthesis of the C1-C28 sector of spongistatin 1 (altohyrtin A). Zuev D; Paquette LA Org Lett; 2000 Mar; 2(5):679-82. PubMed ID: 10814408 [TBL] [Abstract][Full Text] [Related]
9. The stereocontrolled total synthesis of altohyrtin A/spongistatin 1: the southern hemisphere EF segment. Paterson I; Coster MJ; Chen DY; Aceña JL; Bach J; Keown LE; Trieselmann T Org Biomol Chem; 2005 Jul; 3(13):2420-30. PubMed ID: 15976859 [TBL] [Abstract][Full Text] [Related]
10. Synthesis of a C(29)-C(51) subunit of spongistatin 1 (Altohyrtin A) starting from (R)-3-benzyloxy-2-methylpropan-1-ol. Lemaire-Audoire S; Vogel P J Org Chem; 2000 Jun; 65(11):3346-56. PubMed ID: 10843616 [TBL] [Abstract][Full Text] [Related]
11. Synthesis of the C16-C28 spiroketal subunit of spongistatin 1 (altohyrtin A): the pyrone approach. Crimmins MT; Katz JD Org Lett; 2000 Apr; 2(7):957-60. PubMed ID: 10768196 [TBL] [Abstract][Full Text] [Related]
12. Organocatalytic enantioselective Michael addition of cyclic hemiacetals to nitroolefins: a facile access to chiral substituted 5- and 6-membered cyclic ethers. Zhu Y; Qian P; Yang J; Chen S; Hu Y; Wu P; Wang W; Zhang W; Zhang S Org Biomol Chem; 2015 Apr; 13(16):4769-75. PubMed ID: 25806618 [TBL] [Abstract][Full Text] [Related]
13. Multigram synthesis of the C29-C51 subunit and completion of the total synthesis of altohyrtin C (spongistatin 2). Heathcock CH; McLaughlin M; Medina J; Hubbs JL; Wallace GA; Scott R; Claffey MM; Hayes CJ; Ott GR J Am Chem Soc; 2003 Oct; 125(42):12844-9. PubMed ID: 14558833 [TBL] [Abstract][Full Text] [Related]
14. Synthetic studies on the bryostatins: synthetic routes to analogues containing the tricyclic macrolactone core. Keck GE; Truong AP Org Lett; 2005 May; 7(11):2153-6. PubMed ID: 15901157 [TBL] [Abstract][Full Text] [Related]
15. Synthesis and biological evaluation of a spongistatin AB-spiroketal analogue. Smith AB; Corbett RM; Pettit GR; Chapuis JC; Schmidt JM; Hamel E; Jung MK Bioorg Med Chem Lett; 2002 Aug; 12(15):2039-42. PubMed ID: 12113837 [TBL] [Abstract][Full Text] [Related]
17. Total synthesis of (+)-spongistatin 1. An effective second-generation construction of an advanced EF Wittig salt, fragment union, and final elaboration. Smith AB; Zhu W; Shirakami S; Sfouggatakis C; Doughty VA; Bennett CS; Sakamoto Y Org Lett; 2003 Mar; 5(5):761-4. PubMed ID: 12605509 [TBL] [Abstract][Full Text] [Related]