Search Results - "NAKATA, Tadashi"

Refine Results
  1. 1

    Total Synthesis of Marine Polycyclic Ethers by Nakata, Tadashi

    Published in Chemical reviews (01-12-2005)
    “…Since the first isolation of BTX-B in 1981, the unprecedented structure and potent bioactivity of marine polycyclic ethers have attracted much attention of…”
    Get full text
    Journal Article
  2. 2

    SmI2-induced cyclizations and their applications in natural product synthesis by Nakata, Tadashi

    Published in Chemical record (01-06-2010)
    “…Since the isolation of brevetoxin‐B, a red tide toxin, many bioactive marine natural products featuring synthetically challenging trans‐fused polycyclic ether…”
    Get full text
    Journal Article
  3. 3

    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 by Saito, Tatsuo, Nakata, Tadashi

    Published in Organic letters (01-01-2009)
    “…Stereoselective synthesis of a trans-fused 7,6,6,7-membered tetracyclic ether, corresponding to the EFGH-ring of gambierol and the BCDE-ring of gambieric…”
    Get full text
    Journal Article
  4. 4

    C2-Symmetric Chiral Pentacyclic Guanidine: A Phase-Transfer Catalyst for the Asymmetric Alkylation of tert-Butyl Glycinate Schiff Base by Kita, Tetsuya, Georgieva, Angelina, Hashimoto, Yuichi, Nakata, Tadashi, Nagasawa, Kazuo

    Published in Angewandte Chemie International Edition (02-08-2002)
    “…The enantioselective alkylation of the Schiff base 2 was carried out in the presence of a novel phase‐transfer catalyst, the guanidine‐containing pentacyclic…”
    Get full text
    Journal Article
  5. 5

    Synthetic Studies on Maitotoxin. 1. Stereoselective Synthesis of the C′D′E′F′-Ring System Having a Side Chain by Morita, Masayuki, Ishiyama, Seishi, Koshino, Hiroyuki, Nakata, Tadashi

    Published in Organic letters (01-05-2008)
    “…The stereoselective synthesis of the maitotoxin C′D′E′F′-ring system having a side chain has been accomplished through a convergent strategy. The key reactions…”
    Get full text
    Journal Article
  6. 6

    Synthetic Studies on Maitotoxin. 2. Stereoselective Synthesis of the WXYZA′-Ring System by Morita, Masayuki, Haketa, Tasuku, Koshino, Hiroyuki, Nakata, Tadashi

    Published in Organic letters (01-05-2008)
    “…The stereoselective synthesis of the WXYZA′-ring system of maitotoxin has been accomplished via a linear synthetic approach, in which key reactions were…”
    Get full text
    Journal Article
  7. 7

    Discovery of novel antiviral agents directed against the influenza A virus nucleoprotein using photo-cross-linked chemical arrays by Hagiwara, Kyoji, Kondoh, Yasumitsu, Ueda, Atsushi, Yamada, Kazunori, Goto, Hideo, Watanabe, Toshiki, Nakata, Tadashi, Osada, Hiroyuki, Aida, Yoko

    “…The nucleoprotein (NP) of the influenza virus is expressed in the early stage of infection and plays important roles in numerous steps of viral replication. NP…”
    Get full text
    Journal Article
  8. 8

    Synthetic Studies on Maitotoxin. 3. Stereoselective Synthesis of the BCDE-Ring System by Satoh, Masanori, Koshino, Hiroyuki, Nakata, Tadashi

    Published in Organic letters (01-05-2008)
    “…The stereoselective synthesis of the BCDE-ring system of maitotoxin has been accomplished through a two-directional strategy for the construction of polycyclic…”
    Get full text
    Journal Article
  9. 9

    Pheromone Gland-Specific Fatty-Acyl Reductase of the Silkmoth, Bombyx mori by Moto, Ken'ichi, Yoshiga, Toyoshi, Yamamoto, Masanobu, Takahashi, Shunya, Okano, Kazuhiro, Ando, Tetsu, Nakata, Tadashi, Matsumoto, Shogo

    “…The C10-C18unsaturated, acyclic, aliphatic compounds that contain an oxygenated functional group (alcohol, aldehyde, or acetate ester) are a major class of sex…”
    Get full text
    Journal Article
  10. 10

    New synthetic method for 2,3- trans-2-methyl-tetrahydropyran-3-ol and oxepan-3-ol by unique insertion of a methyl group by Kimishima, Atsushi, Nakata, Tadashi

    Published in Tetrahedron letters (10-11-2008)
    “…Treatment of tetrahydropyran-3-ol and oxepan-3-ol derivatives, which have a 1′-mesyloxy group at the C-2 side chain, with Me 3Al effected removal of the…”
    Get full text
    Journal Article
  11. 11

    Stereoselective Synthesis of 2,6-syn-Dimethyl-tetrahydropyran Derivatives, Important Segments of Marine Polycyclic Ethers, by Unique Insertion of the Methyl Group by Maemoto, Michihiro, Kimishima, Atsushi, Nakata, Tadashi

    Published in Organic letters (05-11-2009)
    “…Treatment of 6-methyl-tetrahydropyran derivatives, which have a 1′-mesyloxy group at the C2-side chain, with Me3Al effected stereoselective insertion of a…”
    Get full text
    Journal Article
  12. 12

    Total Synthesis of an Antitumor Agent, Mucocin, Based on the “Chiron Approach” by Takahashi, Shunya, Nakata, Tadashi

    Published in Journal of organic chemistry (09-08-2002)
    “…The total synthesis of a powerful antitumor acetogenin, mucocin (1), was achieved through a palladium-catalyzed cross-coupling reaction of the THP−THF fragment…”
    Get full text
    Journal Article
  13. 13

    Total Synthesis of the Proposed Structure for Pyragonicin by Takahashi, Shunya, Ogawa, Narihito, Koshino, Hiroyuki, Nakata, Tadashi

    Published in Organic letters (23-06-2005)
    “…The total synthesis of acetogenin 1 reported for pyragonicin and its 10-epimer 32 is described. The common THP ring system was stereoselectively constructed…”
    Get full text
    Journal Article
  14. 14
  15. 15

    Total Synthesis of a Cytotoxic Acetogenin, Pyranicin by Takahashi, Shunya, Kubota, Akemi, Nakata, Tadashi

    Published in Organic letters (17-04-2003)
    “…The first total synthesis of a new cytotoxic acetogenin, pyranicin (1), is described. SmI2-induced reductive cyclization of β-alkoxy acrylate 4 proceeded…”
    Get full text
    Journal Article
  16. 16

    Convergent Synthesis of the ABCDEF-Ring System of Yessotoxin and Adriatoxin by Suzuki, Keisuke, Nakata, Tadashi

    Published in Organic letters (31-10-2002)
    “…The convergent synthesis of the ABCDEF-ring system of yessotoxin and adriatoxin was accomplished. This efficient convergent strategy was performed on the basis…”
    Get full text
    Journal Article
  17. 17
  18. 18

    Efficient Synthesis of trans-Fused Polycyclic Ethers Including Tetrahydropyrans and Oxepanes Based on SmI2-Induced Reductive Cyclization by Hori, Nobuyuki, Matsukura, Hiroko, Nakata, Tadashi

    Published in Organic letters (07-10-1999)
    “…An efficient method for the synthesis of trans-fused polycyclic ether ring systems including tetrahydropyrans and oxepanes, i.e., six−seven−six-,…”
    Get full text
    Journal Article
  19. 19
  20. 20

    Stereoselective Syntheses of the C‘D‘E‘F‘-Ring System of Maitotoxin and the FG-Ring System of Gambierol by Sakamoto, Yasuharu, Matsuo, Goh, Matsukura, Hiroko, Nakata, Tadashi

    Published in Organic letters (23-08-2001)
    “…The stereoselective syntheses of the C‘D‘E‘F‘-ring system of maitotoxin and the FG-ring system of gambierol were accomplished. The key steps involve…”
    Get full text
    Journal Article