Prev. Article Next Article Table of Contents

Note

Total Synthesis of Indoles from Tricholoma Species via Bartoli/Heteroaryl Radical Methodologies

Adrian Dobbs*

Department of Chemistry, The Open University, Walton Hall, Milton Keynes MK7 6AA, U.K. A.P.Dobbs@open.ac.uk

J. Org. Chem., 2001, 66 (2), pp 638–641

DOI: 10.1021/jo0057396

Publication Date (Web): December 22, 2000

To whom correspondence should be addressed. Fax: +44 1908 858327.

View: Full Text HTML | Hi-Res PDF

Tools

SciFinder Links

History

Published In Issue January 26, 2001
Received November 20, 2000

Recommend & Share

Related Content

Enantiospecific Total Syntheses of Kapakahines B and FJournal of the American Chemical Society
- Enantiospecific Total Syntheses of Kapakahines B and F
  Timothy Newhouse, Chad A. Lewis and Phil S. Baran
  Journal of the American Chemical Society 2009 131 (18), pp 6360–6361
  Abstract: Gram-scale, enantiospecific total syntheses of the anti-leukemia marine natural products kapakahines B and F have been completed. Two powerfully simplifying transformations have enabled the gram-scale synthesis of this natural product family: (1) an ...
  Abstract | Full Text HTML | PDF w/ Links | Hi-Res PDF
A Flexible, Convergent Approach to Polycyclic Indole Structures: Formal Synthesis of (±)-MersicarpineOrganic Letters
- A Flexible, Convergent Approach to Polycyclic Indole Structures: Formal Synthesis of (±)-Mersicarpine
  Aurlien Biechy and Samir Z. Zard
  Organic Letters 2009 11 (13), pp 2800–2803
  Abstract: The formal synthesis of (±)-mersicarpine was achieved using an intermolecular radical addition−radical cyclization cascade. This key reaction represents a flexible, convergent route to numerous polycyclic indole derivatives.
  Abstract | Full Text HTML | PDF w/ Links | Hi-Res PDF
Asymmetric [4 + 3] Cycloadditions between Vinylcarbenoids and Dienes: Application to the Total Synthesis of the Natural Product (−)-5-epi-Vibsanin EJournal of the American Chemical Society
- Asymmetric [4 + 3] Cycloadditions between Vinylcarbenoids and Dienes: Application to the Total Synthesis of the Natural Product (−)-5-epi-Vibsanin E
  Brett D. Schwartz, Justin R. Denton, Yajing Lian, Huw M. L. Davies and Craig M. Williams
  Journal of the American Chemical Society 2009 131 (23), pp 8329–8332
  Abstract: The total synthesis of (−)-5-epi-vibsanin E (2) has been achieved in 18 steps. The synthesis combines the rhodium-catalyzed [4 + 3] cycloaddition between a vinylcarbenoid and a diene to rapidly generate the tricyclic core with an effective end game ...
  Abstract | Full Text HTML | PDF w/ Links | Hi-Res PDF

Note

Total Synthesis of Indoles from Tricholoma Species via Bartoli/Heteroaryl Radical Methodologies

Tools

SciFinder Links

History

Recommend & Share

Related Content

Enantiospecific Total Syntheses of Kapakahines B and F

A Flexible, Convergent Approach to Polycyclic Indole Structures: Formal Synthesis of (±)-Mersicarpine

Asymmetric [4 + 3] Cycloadditions between Vinylcarbenoids and Dienes: Application to the Total Synthesis of the Natural Product (−)-5-epi-Vibsanin E

Other ACS content by these authors:

JOURNALS

BOOKS

MAGAZINE

COMMUNITIES

DIRECTORIES & DATABASES