Regioselective palladium (O) catalyzed azidation and amination of 1-alkenylcyclpropyl esters: a new route to 2,3-methanoamino acids.

Tetrahedron Letters

Volumn 34, Issue 26, 1993, Pages 4193-4196

  Aufranc, Pierre ^a   Ollivier, Jean ^a   Stolle, Andreas ^a,b   Bremer, Claudia ^a,b   Es Sayed, Mazen ^a,b   de Meijere, Armin ^b   Salaün, Jacques ^a  

^a UNIVERSITÉ PARIS SUD   (France)

^b UNIVERSITY OF GÖTTINGEN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ALIPHATIC AMINE; AMINE; CYCLOPROPANE DERIVATIVE; CYCLOPROPANECARBOXYLIC ACID DERIVATIVE;

ARTICLE; PRIORITY JOURNAL; REACTION ANALYSIS; SYNTHESIS;

EID: 0027298752     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)60525-7     Document Type: Article

References (23)

1. REARRANGEMENT OF ALLYLIC AZIDES
2. Studies on the Preparation and Rearrangements of Allylic Azides1
3. On the Regioselectivity of Palladium(0)-Catalyzed Substitutions on Cyclopropyl Group Containing Allyl Esters1
4. Ultrasound-Promoted Acyloin Condensation and Cyclization of Carboxylic Esters
5. Cyclopropanone hemiacetals
6. A new and convenient preparation of 1-aminocyclopropanecarboxylic acid from acrolein