Diels-Alder reactions of 1,3-dienylboronates as a new route to functionalized carbocycles.
- 31 December 1987
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 28 (36) , 4169-4172
- https://doi.org/10.1016/s0040-4039(00)95569-2
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- A regioselective synthesis of 2-tributylstannyl-1,3-dienesTetrahedron Letters, 1987
- Optically Active ?-Chloro-(E)-crotylboronate Esters by Allyl RearrangementAngewandte Chemie International Edition in English, 1986
- Chiral synthesis via organoboranes. 4. Synthetic utility of boronic esters of essentially 100% optical purity. Synthesis of homologated boronic acids and esters of very high enantiomeric puritiesThe Journal of Organic Chemistry, 1985
- Regiospecific cycloaddition reactions using functionalized isoprenylsilane and related compoundsTetrahedron Letters, 1985
- Diastereogenic Addition of Crotylmetal Compounds to AldehydesAngewandte Chemie International Edition in English, 1982
- The reaction of B-alkyl-9-borabicyclo[3.3.1]nonanes with aldehydes and ketones. A facile elimination of the alkyl group by aldehydesJournal of Organometallic Chemistry, 1978
- Allyl silanes in organic synthesis: some reactions of 3-trimethylsilylcyclohex-4-ene-1,2-dicarboxylic acid and its derivativesJournal of the Chemical Society, Chemical Communications, 1976
- Regioselectivity in the Diels–Alder reaction of 1-trimethylsilylbutadieneJournal of the Chemical Society, Chemical Communications, 1976
- Borverbindungen, XIIQuantitative Bestimmung verschiedener B‐Funktionen in organischen Borverbindungen durch Oxydation mit Trimethylamin‐N‐oxidEuropean Journal of Organic Chemistry, 1967