Sequential Staudinger/Pictet–Spengler cyclization strategy for the construction of tetrahydroisoquinolines of the bioxalomycin and ecteinascidin family of alkaloids-Reference-Cited by-同舟云学术

Sequential Staudinger/Pictet–Spengler cyclization strategy for the construction of tetrahydroisoquinolines of the bioxalomycin and ecteinascidin family of alkaloids

Published:2001-01 Issue:4 Volume:42 Page:543-546
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Herberich Brad,Kinugawa Masahiko,Vazquez Alfredo,Williams Robert M

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference18 articles.

1. (a) Zaccardi, J.; Alluri, M.; Ashcroft, J.; Bernan, V.; Korshalla, J. D.; Morton, G. O.; Siegel, M., Tsao, R.; Williams, D. R.; Maiese, W.; Ellestad, G. A. J. Org. Chem. 1994, 59, 4045–4047;

2. (b) Bernan, V. S.; Montenegro, D. A.; Korshalla, J. D.; Maiese, W. M.; Steinberg, D. A.; Greenstein, M., J. Antibiot. 1994, 47, 1417–1424;

3. (c) Singh, M. P.; Peterson, P. J.; Jacobus, N. V.; Maiese, W. M.; Greenstein, M.; Steinberg, D. A. Antimicrob. Agents Chemother. 1994, 38, 1808–1812.

4. The structure of a novel antitumor antibiotic, saframycin A

5. (a) Rinehart, K. L., Holt, T. G.; Fregeau, N. L.; Keifer, P. A.; Wilson, G. R.; Perun, T. J.; Sakai, R.; Thompson, A. G.; Stroh, J. G.; Shield, L. S.; Seigler, D. S. J. Nat. Prod. 1990, 53, 771–792;

Cited by 48 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Dearomative logic in natural product total synthesis;Natural Product Reports;2022

2. Synthetic and Mechanistic Study of the Catalytic Enantioselective Preparation of Primary β-Amino Ketones from Enones and a Fluorinated Gabriel Reagent;ACS Catalysis;2014-12-09

3. Scandium(III) triflate mediated intramolecular ring expansion of aziridines: a direct access to 4-aryltetrahydroisoquinolines;Tetrahedron Letters;2014-12

4. Protection for the Amino Group;Greene's Protective Groups in Organic Synthesis;2014-08-11

5. Chemistry of renieramycins. Part 12: An improved total synthesis of (±)-renieramycin G;Tetrahedron;2012-06