Crossref Cited-by Linking logo

Collect. Czech. Chem. Commun. 1960, 25, 483-491
https://doi.org/10.1135/cccc19600483

Zur Konfiguration stickstoffhaltiger Verbindungen VII. Absolute Konfiguration von Hydrin und Hydrolin

R. Lukeš, J. Kovář, J. Kloubek and K. Bláha

Crossref Cited-by Linking

  • Lee Jaedeok, Lee Jae Eun, Ha Hyun-Joon, Son Se In, Lee Won Koo: N-Methylative aziridine ring opening: asymmetric synthesis of hygroline, pseudohygroline, and hygrine. Tetrahedron Letters 2015, 56, 856. <https://doi.org/10.1016/j.tetlet.2014.12.133>
  • Anusha Bheemreddy, Reddy Ummareddy V. Subba, Reddy Basireddy V. Subba, Reddy Cirandur Suresh: Diastereoselective Synthesis of (+)-Pseudohygroline via Proline-catalyzed α-Hydroxylation. Natural Product Communications 2014, 9, 1934578X1400900. <https://doi.org/10.1177/1934578X1400900510>
  • Liniger Marc, Estermann Katja, Altmann Karl-Heinz: Total Synthesis of Hygrolines and Pseudohygrolines. J. Org. Chem. 2013, 78, 11066. <https://doi.org/10.1021/jo4017343>
  • McGaw B A, Woolley J G: The Separate Roles of Hygrine Enantiomers in the Biosynthesis of Tropane Alkaloids. Journal of Pharmacy and Pharmacology 2011, 29, 16P. <https://doi.org/10.1111/j.2042-7158.1977.tb11484.x>
  • McGaw B A, Woolley J G: The Stereochemical Integrity of Hygrine Enantiomers in vivo and in vitro. Journal of Pharmacy and Pharmacology 2011, 31, 7P. <https://doi.org/10.1111/j.2042-7158.1979.tb11555.x>
  • Yadav J.S., Narasimhulu G., Mallikarjuna Reddy N., Subba Reddy B.V.: Total synthesis of (+)-pseudohygroline. Tetrahedron Letters 2010, 51, 1574. <https://doi.org/10.1016/j.tetlet.2010.01.060>
  • Davies Stephen G., Fletcher Ai M., Roberts Paul M., Smith Andrew D.: Asymmetric synthesis of Sedum alkaloids via lithium amide conjugate addition. Tetrahedron 2009, 65, 10192. <https://doi.org/10.1016/j.tet.2009.09.104>
  • Lee Jeong-Hee, Jeong Byeong-Seon, Ku Jin-Mo, Jew Sang-sup, Park Hyeung-geun: Total Synthesis of (+)-Hygrine via Asymmetric Phase-Transfer Catalytic Alkylation. J. Org. Chem. 2006, 71, 6690. <https://doi.org/10.1021/jo061108l>
  • e Silva Maria Joselice, Cottier Louis, Srivastava Rajendra M., Sinou Denis, Thozet Alain: Total synthesis and identification of two diastereoisomers of 1-methyl-2-[N-(p-tolylsulfonyl)-2-pyrrolidinyl]ethyl β-l-fucopyranoside. Carbohydrate Research 2005, 340, 309. <https://doi.org/10.1016/j.carres.2004.11.016>
  • Kasai Yusuke, Taji Hiromi, Fujita Takuma, Yamamoto Yoko, Akagi Megumi, Sugio Akinori, Kuwahara Shunsuke, Watanabe Masataka, Harada Nobuyuki, Ichikawa Akio, Schurig Volker: MαNP acid, a powerful chiral molecular tool for preparation of enantiopure alcohols by resolution and determination of their absolute configurations by the 1H NMR anisotropy method. Chirality 2004, 16, 569. <https://doi.org/10.1002/chir.20077>
  • Bates Roderick W., Sa-Ei Kanicha: Syntheses of the sedum and related alkaloids. Tetrahedron 2002, 58, 5957. <https://doi.org/10.1016/S0040-4020(02)00584-7>
  • Enierga Gina, Espiritu Maria, Perlmutter Patrick, Pham Ngoc, Rose Mark, Sjöberg Stefan, Thienthong Neeranat, Wong Katie: Intramolecular amidomercurations under allylic control: a stereoselective synthesis of (+)-pseudohygroline and (+)-3-hydroxypyrrolizidine. Tetrahedron: Asymmetry 2001, 12, 597. <https://doi.org/10.1016/S0957-4166(01)00064-7>
  • Knight David W., Salter Rhys: Activation of the reverse-Cope elimination by allylic oxygen functions: Syntheses of (−)-hygroline and (+)-pseudohygroline. Tetrahedron Letters 1999, 40, 5915. <https://doi.org/10.1016/S0040-4039(99)01131-4>
  • Enierga Gina, Hockless David C.R., Perlmutter Patrick, Rose Mark, Sjöberg Stefan, Wong Katie: An enantioselective synthesis of (+)-pseudohygroline. Tetrahedron Letters 1998, 39, 2813. <https://doi.org/10.1016/S0040-4039(98)00253-6>
  • Takahata Hiroki, Kubota Minoru, Momose Takefumi: New synthesis of all the four isomers of 2-(2-hydroxypropyl)pyrrolidines via iterative asymmetric dihydroxylation to cause enantiomeric enhancement. Tetrahedron: Asymmetry 1997, 8, 2801. <https://doi.org/10.1016/S0957-4166(97)00348-0>
  • San Martín Aurelio, Rovirosa Juana, Gambaro Vicente, Castillo Mariano: Tropane alkaloids from Schizanthus hookeri. Phytochemistry 1980, 19, 2007. <https://doi.org/10.1016/0031-9422(80)83023-8>
  • McGaw Brian A., Woolley Jack G.: Metabolism of hygrine in Atropa, Hyoscyamus and Physalis. Phytochemistry 1979, 18, 189. <https://doi.org/10.1016/S0031-9422(00)90951-8>
  • Roessler Felix, Ganzinger Dietmar, Johne Siegfried, Schöpp Emanuel, Hesse Manfred: Ruspolia hypercrateriformisM.R.: Isolierung und Strukturaufklärung von neuen Pyrrolidin‐Alkaloiden. 169. Mitt. über organische Naturstoffe. Helvetica Chimica Acta 1978, 61, 1200. <https://doi.org/10.1002/hlca.19780610336>
  • McGaw Brian A., Woolley Jack G.: Stereochemistry of tropane alkaloid formation in Datura. Phytochemistry 1978, 17, 257. <https://doi.org/10.1016/S0031-9422(00)94158-X>
  • Baralle Francisco E., Gros Eduardo G.: Biosynthesis of cuscohygrine in Atropa belladonna from sodium acetate-2-14C. Phytochemistry 1969, 8, 853. <https://doi.org/10.1016/S0031-9422(00)85872-0>