Synthesis of novel β-carbolines by the pictet-spengler reaction of tryptophan and ninhydrin:: Oxidative rearrangement of yohimbanone to the corresponding β-carboline.

被引:0
作者
Rohanna, JC [1 ]
Leonard, MS [1 ]
机构
[1] Washington & Jefferson Coll, Dept Chem, Washington, PA 15301 USA
来源
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY | 2005年 / 229卷
关键词
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
1159-CHED
引用
收藏
页码:U533 / U533
页数:1
相关论文
共 50 条
  • [21] ORGN 903-Synthesis of pyrrole-fused pteridines via Pictet-Spengler reaction and Smiles rearrangement
    Xiang, Jinbao
    Zheng, Lianyou
    Chen, Feng
    Dang, Qun
    Bai, Xu
    [J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2006, 232
  • [22] Microporous Schiff base network polymer as an efficient catalyst for the synthesis of spirooxindole tetrahydro-β-carbolines via Pictet-Spengler reaction
    Zhang, Yongfei
    Zhang, Jingwen
    Xiao, Jun
    Zhang, Shiqi
    Hui, Yonghai
    Chen, Weiliang
    [J]. RESEARCH ON CHEMICAL INTERMEDIATES, 2024, 50 (04) : 1873 - 1893
  • [23] Use of the Pictet-Spengler reaction for the synthesis of 1,4-disubstituted-1,2,3,4-tetrahydro-β-carbolines and 1,4-disubstituted-β-carbolines:: formation of γ-carbolines
    Kusurkar, Radhika S.
    Alkobati, Nabil A. H.
    Gokule, Anita S.
    Puranik, Vedavati G.
    [J]. TETRAHEDRON, 2008, 64 (08) : 1654 - 1662
  • [24] Synthesis of Novel Isoquinolino[5,4-ab]phenanthridine Derivatives via Pictet-Spengler Reaction
    Tsai, Min-Chen
    Huang, Pei Yu
    Syu, Liang Sheng
    Shih, Tzenge-Lien
    [J]. SYNTHESIS-STUTTGART, 2019, 51 (06): : 1377 - 1382
  • [25] Total Synthesis of Enantiopure Phalarine via a Stereospecific Pictet-Spengler Reaction: Traceless Transfer of Chirality from L-Tryptophan
    Trzupek, John D.
    Lee, Dongjoo
    Crowley, Brendan M.
    Marathias, Vasilios M.
    Danishefsky, Samuel J.
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2010, 132 (24) : 8506 - 8512
  • [26] Practical Stereoselective Synthesis of C3-Spirooxindole- and C2-Spiropseudoindoxyl-Pyrrolidines via Organocatalyzed Pictet-Spengler Reaction/Oxidative Rearrangement Sequence
    Kondo, Masaru
    Matsuyama, Naoki
    Aye, Tin Z.
    Mattan, Irshad
    Sato, Tomoyuki
    Makita, Yoshinori
    Ishibashi, Masami
    Arai, Midori A.
    Takizawa, Shinobu
    Sasai, Hiroaki
    [J]. ADVANCED SYNTHESIS & CATALYSIS, 2021, 363 (10) : 2648 - 2663
  • [27] o-Benzenedisulfonimide as a reusable acid catalyst for an easy, efficient, and green synthesis of tetrahydroisoquinolines and tetrahydro-β-carbolines through Pictet-Spengler reaction
    Barbero, Margherita
    Bazzi, Stefano
    Cadamuro, Silvano
    Dughera, Stefano
    [J]. TETRAHEDRON LETTERS, 2010, 51 (48) : 6356 - 6359
  • [28] Structure and spectral properties of a-carbolines. Part 9. New arguments against direct rearrangement of the spiroindolenine intermediate into a-carboline system in the pictet-spengler cyclization An MNDO approach
    Kowalski, P.
    Mokrosz, J. L.
    [J]. Bulletin des Societes Chimiques Belges, 106 (03):
  • [29] SYNTHESIS OF NOVEL BENZOFURO-FUSED THIAZOLO[3,2-a]-PYRIMIDINONES VIA PICTET-SPENGLER REACTION
    Wang, Dao-Lin
    Wang, Dong
    Qiang, Jian-Hua
    Liu, Lin
    [J]. HETEROCYCLES, 2016, 92 (03) : 552 - 559
  • [30] On Water Pictet-Spengler Reaction of Tryptophan followed by Buchwald Coupling for the Synthesis of Natural Products Stellarines A, B and β-Carboline Derivatives: Their Molecular Docking against SARS-CoV-2 MPro
    Gunjan
    Sharma, Pankaj
    Kumar, Pradeep
    Sharma, Nutan
    Bhagat, Sunita
    [J]. CHEMISTRYSELECT, 2023, 8 (11):