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Home   •   Spotlight  •  rlist2q07j  •  Most Requested Journal Articles 2Q07-Chemistry and Related Science (10)
Most Requested Journal Articles 2Q07-Chemistry and Related Science

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Following is one of the journal articles most requested by researchers using CAS electronic products.


CAS indexed 271 chemical substances from this document.
CAS subject entries for this document include: Addition reaction; Alkenes, reactions; Azides; and 1 additional concept.

CAPLUS COPYRIGHT 2007 ACS on STN

TITLE: Hydrazines and Azides via the Metal-Catalyzed Hydrohydrazination and Hydroazidation of Olefins
AUTHOR(S): Waser, Jerome; Gaspar, Boris; Nambu, Hisanori; Carreira, Erick M.
CORPORATE SOURCE: Laboratorium fuer Organische Chemie, ETH Zuerich, Hoenggerberg HCI-H335, Zurich, 8093, Switz.
SOURCE: Journal of the American Chemical Society (2006), 128(35), 11693-11712 CODEN: JACSAT; ISSN: 0002-7863
PUBLISHER: American Chemical Society
LANGUAGE: English
ABSTRACT:
The discovery, study, and implementation of the Co- and Mn-catalyzed hydrohydrazination and hydroazidation reactions of olefins are reported. These reactions are equiv. to direct hydroaminations of C-C double bonds with protected hydrazines or hydrazoic acid but are based on a different concept in which the H and the N atoms come from two different reagents, a silane and an oxidizing nitrogen source (azodicarboxylate or sulfonyl azide). The hydrohydrazination reaction using di-tert-Bu azodicarboxylate is characterized by its ease of use, large functional group tolerance, and broad scope, including mono-, di-, tri-, and tetrasubstituted olefins. Key to the development of the hydroazidation reaction was the use of sulfonyl azides as nitrogen sources and the activating effect of tert-Bu hydroperoxide. The reaction was found to be efficient for the functionalization of mono-, di-, and trisubstituted olefins, and only a few functional groups are not tolerated. The alkyl azides obtained are versatile intermediates and can be transformed to the free amines or triazoles without isolation of the azides. Preliminary mechanistic investigations suggest a rate-limiting hydrocobaltation of the alkene, followed by an amination reaction. Radical intermediates cannot be ruled out and may be involved.  

Updated 8/24/2007 12:28:13 PM
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