منابع مشابه
REACTION OF VINYLENE TRITHIOCARBONATE WITH CHLOROSULFONYL ISOCYANATE
The reaction between vinylene trithiocarbonate and chlorosulfonyl isocyanate proceeds by initial attack of thiocarbonyl on the isocyanate carbon.
متن کاملreaction of vinylene trithiocarbonate with chlorosulfonyl isocyanate
the reaction between vinylene trithiocarbonate and chlorosulfonyl isocyanate proceeds by initial attack of thiocarbonyl on the isocyanate carbon.
متن کاملRegioselective and diastereoselective amination with use of chlorosulfonyl isocyanate: a short and efficient synthesis of (-)-cytoxazone.
The total synthesis of (-)-cytoxazone 1 was achieved in six linear steps (34% overall yield) from p-anisaldehyde. The key steps in this route are the regioselective and stereoselective introduction of a N-protected amine group, using the CSI reaction of the anti-1,2-dimethyl ether 3, and the subsequent regioselective cyclization of the N-protected amino diol 13 to give the 2-oxazolidinone unit ...
متن کاملNovel synthetic method for allylic amination of cyclic allylic ethers using chlorosulfonyl isocyanate
Article history: Received 13 December 2010 Revised 1 February 2011 Accepted 9 February 2011 Available online 13 February 2011
متن کاملAsymmetric total synthesis of (+)-indatraline via diastereoselective amination of chiral ethers using chlorosulfonyl isocyanate
A concise asymmetric total synthesis of (þ)-indatraline from readily available cinnamic acid is described. The key steps include Corey’s oxazaborolidine-catalyzed asymmetric carbonyl reduction and a highly stereoselective amination of chiral benzylic ether with retention of stereochemistry using chlorosulfonyl isocyanate. 2013 Elsevier Ltd. All rights reserved.
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ژورنال
عنوان ژورنال: Journal of Synthetic Organic Chemistry, Japan
سال: 1988
ISSN: 0037-9980,1883-6526
DOI: 10.5059/yukigoseikyokaishi.46.1209