English
 
User Manual Privacy Policy Disclaimer Contact us
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT
  Base-Promoted Internal Redox-Cyclisation Reactions

Shaaban, S., Peng, B., & Maulide, N. (2013). Base-Promoted Internal Redox-Cyclisation Reactions. Synlett, 24(13), 1722-1724. doi:10.1055/s-0033-1339313.

Item is

Basic

show hide
Item Permalink: http://hdl.handle.net/11858/00-001M-0000-0014-A395-0 Version Permalink: http://hdl.handle.net/11858/00-001M-0000-001A-1540-4
Genre: Journal Article

Files

show Files

Locators

show

Creators

show
hide
 Creators:
Shaaban, Saad1, Author              
Peng, Bo1, Author              
Maulide, Nuno1, Author              
Affiliations:
1Research Group Maulide, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445614              

Content

show
hide
Free keywords: C-H activation - C-H functionalisation - redox - cyclisation - pyrrolidine
 Abstract: A new internal, base-mediated redox-cyclisation reaction has been discovered and developed. In this transformation, the sacrificial reduction of an alkynyl moiety to an alkene allows direct functionalisation of an α-amino C-H bond. This approach allows the preparation of several 1,3-oxazinane derivatives in an atom-­efficient manner.

Details

show
hide
Language(s): eng - English
 Dates: 2013-07-10
 Publication Status: Published online
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Method: Peer
 Identifiers: DOI: 10.1055/s-0033-1339313
 Degree: -

Event

show

Legal Case

show

Project information

show

Source 1

show
hide
Title: Synlett
  Other : Synlett
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: -
Pages: - Volume / Issue: 24 (13) Sequence Number: - Start / End Page: 1722 - 1724 Identifier: ISSN: 0936-5214
CoNE: /journals/resource/954925570856