@article {2055,
	title = {A synthetic approach to the fusicoccane A-B ring fragment based on a Pauson-Khand cycloaddition/Norrish type 1 fragmentation},
	journal = {Journal of Organic Chemistry},
	volume = {73},
	number = {17},
	year = {2008},
	note = {ISI Document Delivery No.: 344EDTimes Cited: 1Cited Reference Count: 88Dake, Gregory R. Fenster, Erik E. Patrick, Brian O.},
	month = {Sep},
	pages = {6711-6715},
	type = {Article},
	abstract = {A synthetic approach to the A-B ring system within the fusicoccane family of diterpenes is presented. Key steps in this approach are a diastereoselective Pauson-Khand reaction, a Norrish 1 photofragmentation, a Charette cyclopropanation, and a ring-closing metathesis process.},
	keywords = {ALLYLIC ALCOHOLS, BICYCLIC SYSTEMS, CARBONYL-COMPOUNDS, CEROPLASTIN NUCLEUS, CLOSING METATHESIS, CYCLIZATION, DOLASTANE DITERPENES, ENYNE METATHESIS, NATURAL-PRODUCTS, NAZAROV, ORGANIC-SYNTHESIS},
	isbn = {0022-3263},
	url = {<Go to ISI>://000258908000030},
	author = {Dake, G. R. and Fenster, E. E. and Patrick, B. O.}
}
@article {7193,
	title = {CONTROL OF REGIOSELECTIVITY THROUGH RELIEF OF STERIC CROWDING IN THE DI-PI-METHANE PHOTOREARRANGEMENT OF 9,10-ETHENOANTHRACENE DERIVATIVES},
	journal = {Tetrahedron Letters},
	volume = {33},
	number = {12},
	year = {1992},
	note = {ISI Document Delivery No.: HJ784Times Cited: 4Cited Reference Count: 13},
	month = {Mar},
	pages = {1535-1538},
	type = {Article},
	abstract = {Product structures and quantum yields for the solution phase di-pi-methane photorearrangement of the 9,10-ethenoanthracene derivatives 1-4 have been determined. The results are consistent with a model in which relief of steric crowding is the factor that governs regioselectivity.},
	keywords = {BICYCLIC SYSTEMS, NITROBENZOATES, REARRANGEMENTS, solvolysis},
	isbn = {0040-4039},
	url = {<Go to ISI>://A1992HJ78400002},
	author = {Chen, J. X. and Pokkuluri, P. R. and Scheffer, J. R. and Trotter, J.}
}
@article {7193,
	title = {CONTROL OF REGIOSELECTIVITY THROUGH RELIEF OF STERIC CROWDING IN THE DI-PI-METHANE PHOTOREARRANGEMENT OF 9,10-ETHENOANTHRACENE DERIVATIVES},
	journal = {Tetrahedron Letters},
	volume = {33},
	number = {12},
	year = {1992},
	note = {ISI Document Delivery No.: HJ784Times Cited: 4Cited Reference Count: 13},
	month = {Mar},
	pages = {1535-1538},
	type = {Article},
	abstract = {Product structures and quantum yields for the solution phase di-pi-methane photorearrangement of the 9,10-ethenoanthracene derivatives 1-4 have been determined. The results are consistent with a model in which relief of steric crowding is the factor that governs regioselectivity.},
	keywords = {BICYCLIC SYSTEMS, NITROBENZOATES, REARRANGEMENTS, solvolysis},
	isbn = {0040-4039},
	url = {<Go to ISI>://A1992HJ78400002},
	author = {Chen, J. X. and Pokkuluri, P. R. and Scheffer, J. R. and Trotter, J.}
}
