Alternative Spiroketalization Methods toward Purpuromycin: A Hemiketal Conjugate Addition Strategy and Use of an Electron-Rich Isocoumarin Precursor

被引:18
作者
Bandichhor, Rakeshwar [1 ]
Lowell, Andrew N. [1 ]
Kozlowski, Marisa C. [1 ]
机构
[1] Univ Penn, Dept Chem, Roy & Diana Vagelos Labs, Philadelphia, PA 19104 USA
基金
美国国家科学基金会;
关键词
ALPHA-RUBROMYCIN; CONVERGENT ROUTE; HUMAN TELOMERASE; DNA HELICASE; (+/-)-GAMMA-RUBROMYCIN; HELIQUINOMYCIN; INHIBITION; BIKAVERIN; SYSTEM; MODEL;
D O I
10.1021/jo200398v
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Two methods are presented that were designed to circumvent the persistent problem of benzofuran formation and instead yield a spiroketal of the rubromycin family type. First, using an alternative disconnection, a hemiketal conjugate addition to a naphthaquinone electrophile was investigated. Synthesis of the requisite electrophile provided insight into the selective oxidation and functionalization of the naphthalene portion. Second, the electronic features of the isocoumarin ring system were adjusted, and the corresponding reactivity further supports the hypothesis that electron-rich isocoumarins are capable of spiroketalization. Robust, flexible syntheses from simple precursors were developed that allowed multiple reduced isocoumarins to be generated. Combined, the data presented herein give insight into the sensitivities of this family and illuminate other potential methods of spiroketalization. In addition, the convergent assembly of substrates containing different naphthaquinone and isocoumarin subunits highlights the utility of our 1,3-dipolar cycloaddition approach to generate analogs of these structures for SAR, as well as chemical reactivity studies.
引用
收藏
页码:6475 / 6487
页数:13
相关论文
共 42 条
  • [1] Total synthesis of (±)-γ-Rubromycin on the basis of two aromatic pummerer-type reactions
    Akai, Shuji
    Kakiguchi, Keisuke
    Nakamura, Yuka
    Kuriwaki, Ikumi
    Dohi, Toshifumi
    Harada, Shusaku
    Kubo, Ozora
    Morita, Nobuyoshi
    Kita, Yasuyuki
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2007, 46 (39) : 7458 - 7461
  • [2] RULES FOR RING-CLOSURE
    BALDWIN, JE
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1976, (18) : 734 - 736
  • [3] BARDONE MR, 1974, TETRAHEDRON, V30, P2747, DOI 10.1016/S0040-4020(01)97439-3
  • [4] Total synthesis of phomazarin
    Boger, DL
    Hong, JY
    Hikota, M
    Ishida, M
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (11) : 2471 - 2477
  • [5] Rubromycins:: Structurally intriguing, biologically valuable, synthetically challenging antitumour antibiotics
    Brasholz, Malte
    Soergel, Sebastian
    Azap, Cengiz
    Reissig, Hans-Ulrich
    [J]. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2007, 2007 (23) : 3801 - 3814
  • [6] RUBROMYCINS .3. CONSTITUTION OF ALPHA-RUBROMYCIN, BETA-RUBROMYCIN, GAMMA-RUBROMYCIN, AND GAMMA-ISO-RUBROMYCIN
    BROCKMAN.H
    ZEECK, A
    [J]. CHEMISCHE BERICHTE-RECUEIL, 1970, 103 (06): : 1709 - &
  • [7] RUBROMYCIN, EIN ROTES ANTIBIOTIKUM AUS ACTINOMYCETEN
    BROCKMANN, H
    RENNEBERG, KH
    [J]. NATURWISSENSCHAFTEN, 1953, 40 (02) : 59 - 60
  • [8] Heliquinomycin, a new inhibitor of DNA helicase, produced by Streptomyces sp MJ929-SF2 .2. Structure determination of heliquinomycin
    Chino, M
    Nishikawa, K
    Tsuchida, T
    Sawa, R
    Nakamura, H
    Nakamura, KT
    Muraoka, Y
    Ikeda, D
    Naganawa, H
    Sawa, T
    Takeuchi, T
    [J]. JOURNAL OF ANTIBIOTICS, 1997, 50 (02) : 143 - 146
  • [9] Effect of a novel antibiotic, heliquinomycin, on DNA helicase and cell growth
    Chino, M
    Nishikawa, K
    Yamada, A
    Ohsono, M
    Sawa, T
    Hanaoka, F
    Ishizuka, M
    Takeuchi, T
    [J]. JOURNAL OF ANTIBIOTICS, 1998, 51 (05) : 480 - 486
  • [10] PURPUROMYCIN, A NEW ANTIBIOTIC ISOLATED FROM ACTINOPLANES-IANTHINOGENES N-SP
    CORONELL.C
    PAGANI, H
    BARDONE, MR
    LANCINI, GC
    [J]. JOURNAL OF ANTIBIOTICS, 1974, 27 (03) : 161 - 168