SYNTHESIS OF 1,8-DIAZASPIRO[4.5]DECANE SYSTEM

被引:7
|
作者
WITTEKIN.RR
WEISSMAN, C
机构
关键词
D O I
10.1002/jhet.5570090118
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
引用
收藏
页码:111 / &
相关论文
共 50 条
  • [1] THE SYNTHESIS OF 1,8-DIAZASPIRO[4,5]-DECANES
    VANPARYS, M
    VANDEWALLE, M
    BULLETIN DES SOCIETES CHIMIQUES BELGES, 1981, 90 (07): : 749 - 755
  • [2] 8-L-Cystinyl Bis(1,8-diazaspiro[4.5]decane) as an Orally Bioavailable L-Cystine Crystallization Inhibitor for Cystinuria
    Hu, Longqin
    Albanyan, Haifa
    Yang, Jeffrey
    Wang, Yiling
    Yang, Min
    Tan, Xiangduan
    Zhong, Xiaodi
    Ward, Michael D.
    Sahota, Amrik
    ACS MEDICINAL CHEMISTRY LETTERS, 2024, : 1026 - 1031
  • [3] DERIVATIVES OF 1,3-DIAZASPIRO[4.5]DECANE
    SCHIPPER, E
    CHINERY, E
    JOURNAL OF ORGANIC CHEMISTRY, 1961, 26 (09): : 3597 - &
  • [4] ASYMMETRIC-SYNTHESIS .29. PREPARATION OF 1,8-DIAZASPIRO[5.5]UNDECANE DERIVATIVES
    ZHU, JP
    QUIRION, JC
    HUSSON, HP
    JOURNAL OF ORGANIC CHEMISTRY, 1993, 58 (23): : 6451 - 6456
  • [5] CENTRAL CHOLINERGIC AGENTS .3. SYNTHESIS OF 2-ALKOXY-2,8-DIAZASPIRO[4.5]DECANE-1,3-DIONES AS MUSCARINIC AGONISTS
    ISHIHARA, Y
    YUKIMASA, H
    MIYAMOTO, M
    GOTO, G
    CHEMICAL & PHARMACEUTICAL BULLETIN, 1992, 40 (05) : 1177 - 1185
  • [6] SYNTHESIS OF A NEW SERIES OF 8-SUBSTITUTED-2,8-DIAZASPIRO[4.5]DECAN-3-ONES
    CIGNARELLA, G
    VILLA, S
    BARLOCCO, D
    JOURNAL OF HETEROCYCLIC CHEMISTRY, 1993, 30 (05) : 1357 - 1359
  • [7] 1,4-diazaspiro[4.5]decane-2,3-dione
    Stasko, D
    Davis, MC
    Chapman, RD
    ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS, 2002, 58 : O1384 - O1386
  • [8] One-step synthesis of diazaspiro[4.5]decane scaffolds with exocyclic double bonds
    Li, Lidong
    Hu, Qiong
    Zhou, Pingping
    Xie, Haifeng
    Zhang, Xiaorong
    Zhang, Hao
    Hu, Yadong
    Yin, Fei
    Hu, Yimin
    ORGANIC & BIOMOLECULAR CHEMISTRY, 2014, 12 (29) : 5356 - 5359
  • [9] The Synthesis of Methyl-Substituted Spirocyclic Piperidine-Azetidine (2,7-Diazaspiro[3.5]nonane) and Spirocyclic Piperidine-Pyrrolidine (2,8-Diazaspiro[4.5]decane) Ring Systems
    Smith, Aaron C.
    Cabral, Shawn
    Kung, Daniel W.
    Rose, Colin R.
    Southers, James A.
    Garcia-Irizarry, Carmen N.
    Damon, David B.
    Bagley, Scott W.
    Griffith, David A.
    JOURNAL OF ORGANIC CHEMISTRY, 2016, 81 (09): : 3509 - 3519
  • [10] Spirocyclic nonpeptide glycoprotein IIb-IIIa antagonists -: Part IV:: Modifications of the 2,8-diazaspiro[4.5]decane nucleus.
    Mehrotra, MM
    Heath, J
    Pandey, A
    Smyth, MS
    Rüter, G
    Schotten, T
    Rose, J
    Seroogy, J
    Volkots, DL
    Alaimo, L
    Park, G
    Scarborough, RM
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2000, 219 : U35 - U35