A Self-Immolative Strategy for 1,2-Elimination of Homallyl Sulfones to 1,3-Dienes
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00397918708063902
Reference8 articles.
1. Syntheses Via Vinyl Sulfones 20. For paper 19 see reference 2
2. Conrad, P. C., Kwiatkowski, P. L. and Fuchs, P. L. submitted
3. Recent developments in sulfone chemistry
4. Total synthesis of ionophore antibiotic X-14547A. 2. Coupling of the tetrahydropyran and tetrahydroindan systems and construction of the butadienyl and ketopyrrole moieties
5. A new preparation of enamides and dienamides.
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1. Evolving Organic Synthesis Fostered by the Pluripotent Phenylsulfone Moiety;Chemical Reviews;2009-05-13
2. Synthesis of [Ethylene-1-(η5-4,5,6,7-tetrahydro-1-indenyl)-2- (η5-4‘,5‘,6‘,7‘-tetrahydro-2‘-indenyl)]titanium Dichloride, the Elusive Isomer of the Brintzinger-Type ansa-Titanocenes;The Journal of Organic Chemistry;2003-10-01
3. 2-Methoxyallyl Bromide;Encyclopedia of Reagents for Organic Synthesis;2001-04-15
4. New Synthetic Methods Exploiting Vinyl Sulfones Discovered During the Synthesis of a Natural Product;Phosphorus, Sulfur, and Silicon and the Related Elements;1994-10
5. Carbon–Carbon Double-Bond Formation by Sulphone Elimination;Sulphones in Organic Synthesis;1993
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