New electronically enriched boronobutadienes for the synthesis of hydroxylated cyclohexenes via tandem [4+2]/allylboration
- 14 February 2003
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 44 (10) , 2231-2235
- https://doi.org/10.1016/s0040-4039(03)00164-3
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- A Concise Synthesis of an Advanced Clerodin Intermediate through a Vaultier Tandem ReactionEuropean Journal of Organic Chemistry, 2002
- Tandem Aza[4 + 2]/Allylboration: A Novel Multicomponent Reaction for the Stereocontrolled Synthesis of α-Hydroxyalkyl Piperidine DerivativesOrganic Letters, 2000
- An improvement to the Vaultier tandem sequence: A practical highly stereoselective three-component reactionTetrahedron Letters, 1999
- Diels–Alder reactions of dienylboron compounds with unactivated dienophiles: an application of boron tethering for substituted cyclohexenol synthesisChemical Communications, 1999
- 1,3-dienylboronates in diels-alder reaction: Part IIITetrahedron Letters, 1997
- 1,3-Dienylboronates in Diels-Alder reactions: Part II1Tetrahedron: Asymmetry, 1996
- Diels-Alder reactions of 1,3-dienylborate salts with activated dienophilesTetrahedron Letters, 1996
- Hydroboration of Alkynes with Pinacolborane Catalyzed by HZrCp2ClOrganometallics, 1995
- Lewis base-catalysed asymmetric Diels—Alder reactionJournal of the Chemical Society, Chemical Communications, 1991
- Diels-Alder reactions of 1,3-dienylboronates as a new route to functionalized carbocycles.Tetrahedron Letters, 1987