N-prop-2-ynylmaleimide. Application to sequential one-pot Rh(I) catalysed [2+2+2]-alkyne cyclotrimerisation-imine cycloaddition

Citation
R. Grigg et al., N-prop-2-ynylmaleimide. Application to sequential one-pot Rh(I) catalysed [2+2+2]-alkyne cyclotrimerisation-imine cycloaddition, TETRAHEDRON, 56(45), 2000, pp. 8967-8976
Citations number
30
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON
ISSN journal
00404020 → ACNP
Volume
56
Issue
45
Year of publication
2000
Pages
8967 - 8976
Database
ISI
SICI code
0040-4020(20001103)56:45<8967:NATSOR>2.0.ZU;2-R
Abstract
Rh(I) catalysed [2+2+2]-cyclotrimerisation of 1,6-diynes with monoynes in c ombination with stereospecific thermal or Ag(I) catalysed aldimine-->(metal lo) azomethine ylide-->cycloaddition cascades affords rapid access to compl ex heterocyclic benzene derivatives in one-pot processes with the generatio n 5 new bonds, 4 stereocentres and 3 rings. (C) 2000 Elsevier Science Ltd. All rights reserved.