83865-35-4Relevant academic research and scientific papers
Highly functionalised monocyclic and bicyclic β-lactams via alkene metathesis
Barrett, Anthony G. M.,Baugh, Simon P. D.,Gibson, Vernon C.,Giles, Matthew R.,Marshall, Edward L.,Procopiou, Panayiotis A.
, p. 155 - 156 (1997)
Both monocyclic and bicyclic β-lactam systems are prepared via alkene metathesis reactions using Mo(=CHCPhMe2)-(=NC6H3Pr(i)20[(OCMe(CF3)2]2 or Ru(=CHPh)Cl2(PCy3/
Rapid entry into mono-, bi-, and tricyclic β-lactam arrays via alkene metathesis
Barrett, Anthony G. M.,Baugh, Simon P. D.,Christopher Braddock,Flack, Kevin,Gibson, Vernon C.,Giles, Matthew R.,Marshall, Edward L.,Procopiou, Panayiotis A.,White, Andrew J. P.,Williams, David J.
, p. 7893 - 7907 (2007/10/03)
4-Acetoxy-2-azetidinone and (3R,4R)-4-acetoxy-3-[(1R)-1-(tert- butyldimethylsilyl)-oxyethyl]-2-azetidinone were converted into 4-alkenyloxy- , 4-(N-allyltoluene-4-sulfonamido)-, 4-(allylthio)-, and 4-alkenyl-2- azetidinone systems. In addition, 4-acetoxy-2-azetidinone and (3R,4R)-4- acetoxy-3-[(1R)-1-(tert-butyldimethylsilyl)-oxyethyl]-2-azetidinone were converted into β-lactam dienes via sequential C-4 substitution using unsaturated alcohols, allyl mercaptan, N-allyltoluene-4-sulfonamide, and allyl(chloro)dimethylsilane followed by N-allylation. Crossed metathesis of β-lactam alkenes with styrene partners and ring closing metathesis of β- lactam dienes using the Schrock [(CF3)2MeCO]2Mo(=CHCMe2Ph)(=NC6H3-2,6- iso-Pr2) (1) or Grubbs Cl2(Cy3P)2Ru=CHPh (2) carbenes gave diverse monocyclic and bicyclic β-lactam systems including derivatives of 1- azabicyclo-[4.2.0]octan-8-one, 1-azabicyclo[5.2.0]nonan-9-one and its 6- thia, 6-aza, and 6-oxa analogues, 7-oxa-1-azabicyclo[6.2.0]octan-10-one,8- oxa-1-azabicyclo[7.2.0]octan-11-one, and 9-oxa-1-azabicyclo[8.2.0]octan-12- one. Ring-closing enyne metathesis and tandem ring-closing enyne and diene metathetic reactions were used to produce bicyclic β-lactam conjugated dienes as exemplified by the conversion of (3S,4R)-(-)-3-[(1R)-(tert- butyldimethylsilyl)oxyethyl]-1-(5-oxa-oct-7-en-2-yn-1-yl)-4-(2-propenyl)- azetidin-2-one (83) into (6R,7S)-(+)-7-[(1R)-(tert- butyldimethylsilyl)oxyethyl]-3-[(2,5-dihydro)-3-furanyl]-1- azabicyclo[4.2.0]oct-3-en-8-one (98).
NITROGEN NUCLEOPHILE DISPLACEMENTS OF THE ACETATE GROUP FROM 4-ACETOXYAZETIDIN-2-ONE
Campbell, Malcolm M.,Connarty, Bernard P.
, p. 1853 - 1854 (2007/10/02)
N-Tosylamino nucleophiles displaced acetate from 4-acetoxyazetidin-2-one, complementing other studies of heteronucleophiles.Annelation procedures for model 4,6-bicyclic β-lactams were established.
