Intramolecular [4 + 2] Cycloadditions of Benzynes with Conjugated Enynes, Arenynes, and Dienes Export

@article{citeulike:6098020, abstract = {PMID: 16119931 Benzynes generated by the reaction of o-(trimethylsilyl)aryl triflates with TBAT participate in intramolecular [4 + 2] cycloadditions with conjugated enynes, arenynes, and dienes to furnish highly condensed polycyclic aromatic compounds.}, author = {Hayes, Martin E. and Shinokubo, Hiroshi and Danheiser, Rick L.}, citeulike-article-id = {6098020}, citeulike-linkout-0 = {http://dx.doi.org/10.1021/ol051372l}, citeulike-linkout-1 = {http://pubs.acs.org/doi/abs/10.1021/ol051372l}, day = {1}, doi = {10.1021/ol051372l}, journal = {Organic Letters}, keywords = {42, benzyne, cycloaddition, danheiser, enyne, mit}, month = {September}, number = {18}, pages = {3917--3920}, posted-at = {2009-11-11 12:57:20}, priority = {0}, title = {Intramolecular [4 + 2] Cycloadditions of Benzynes with Conjugated Enynes, Arenynes, and Dienes}, url = {http://dx.doi.org/10.1021/ol051372l}, volume = {7}, year = {2005} }

TY - JOUR ID - citeulike:6098020 L3 - citeulike-article-id:6098020 N2 - PMID: 16119931 Benzynes generated by the reaction of o-(trimethylsilyl)aryl triflates with TBAT participate in intramolecular [4 + 2] cycloadditions with conjugated enynes, arenynes, and dienes to furnish highly condensed polycyclic aromatic compounds. IS - 18 JF - Organic Letters EP - 3920 TI - Intramolecular [4 + 2] Cycloadditions of Benzynes with Conjugated Enynes, Arenynes, and Dienes VL - 7 SP - 3917 KW - 42 KW - benzyne KW - cycloaddition KW - danheiser KW - enyne KW - mit AU - Hayes, Martin AU - Shinokubo, Hiroshi AU - Danheiser, Rick PY - 2005/09/01/ UR - http://dx.doi.org/10.1021/ol051372l ER -