@article {2694,
	title = {Construction of Carbo- and Heterocycles Using Radical Relay Cyclizations Initiated by Alkoxy Radicals},
	journal = {Organic Letters},
	volume = {11},
	number = {9},
	year = {2009},
	note = {ISI Document Delivery No.: 438ATTimes Cited: 5Cited Reference Count: 55Zhu, Hai Wickenden, Jason G. Campbell, Natalie E. Leung, Joe C. T. Johnson, Kayll M. Sammis, Glenn M.},
	month = {May},
	pages = {2019-2022},
	type = {Article},
	abstract = {An efficient method for the rapid construction of carbo- and heterocycles has been developed using radical relay cyclizations initiated by alkoxy radicals. Linear substrates were cyclized to form a wide range of cyclopentane, pyrrolidine, tetrahydropyran, and tetrahydrofuran derivatives in excellent yields. This methodology was utilized as a key step in the synthesis of the tetrahydrofuran fragment in (-)-amphidinolide K.},
	keywords = {1, 5-HYDROGEN ATOM TRANSFER, AMPHIDINOLIDE K, C-H ACTIVATION, CARBONYLATION, CHAIN REACTIONS, EFFICIENT, FUNCTIONALIZATION, ORGANIC-SYNTHESIS, REARRANGEMENT, TRANSLOCATION REACTIONS},
	isbn = {1523-7060},
	url = {<Go to ISI>://000265529000039},
	author = {Zhu, H. and Wickenden, J. G. and Campbell, N. E. and Leung, J. C. T. and Johnson, K. M. and Sammis, G. M.}
}
@article {2694,
	title = {Construction of Carbo- and Heterocycles Using Radical Relay Cyclizations Initiated by Alkoxy Radicals},
	journal = {Organic Letters},
	volume = {11},
	number = {9},
	year = {2009},
	note = {ISI Document Delivery No.: 438ATTimes Cited: 5Cited Reference Count: 55Zhu, Hai Wickenden, Jason G. Campbell, Natalie E. Leung, Joe C. T. Johnson, Kayll M. Sammis, Glenn M.},
	month = {May},
	pages = {2019-2022},
	type = {Article},
	abstract = {An efficient method for the rapid construction of carbo- and heterocycles has been developed using radical relay cyclizations initiated by alkoxy radicals. Linear substrates were cyclized to form a wide range of cyclopentane, pyrrolidine, tetrahydropyran, and tetrahydrofuran derivatives in excellent yields. This methodology was utilized as a key step in the synthesis of the tetrahydrofuran fragment in (-)-amphidinolide K.},
	keywords = {1, 5-HYDROGEN ATOM TRANSFER, AMPHIDINOLIDE K, C-H ACTIVATION, CARBONYLATION, CHAIN REACTIONS, EFFICIENT, FUNCTIONALIZATION, ORGANIC-SYNTHESIS, REARRANGEMENT, TRANSLOCATION REACTIONS},
	isbn = {1523-7060},
	url = {<Go to ISI>://000265529000039},
	author = {Zhu, H. and Wickenden, J. G. and Campbell, N. E. and Leung, J. C. T. and Johnson, K. M. and Sammis, G. M.}
}
@article {2341,
	title = {Chemoselective Oxygen-Centered Radical Cyclizations onto Silyl Enol Ethers},
	journal = {Organic Letters},
	volume = {10},
	number = {21},
	year = {2008},
	note = {ISI Document Delivery No.: 367EETimes Cited: 3Cited Reference Count: 37Zlotorzynska, Maria Zhai, Huimin Sammis, Glenn M.},
	month = {Nov},
	pages = {5083-5086},
	type = {Article},
	abstract = {A new oxygen-centered radical cyclization onto silyl enol ethers has been developed and utilized for the synthesis of versatile siloxy-substituted tetrahydrofurans. The reactions display excellent chemoselectivity for cyclization onto the electron-rich silyl enol ether when competing terminal alkene cyclization, 1,5-hydrogen abstraction, and beta-fragmentation pathways are present. The increased chemoselectivity also allows for the synthesis of tetrahydropyrans, a challenging substrate class to access using oxygen-centered radical alkene cyclizations due to competing 1,5-hydrogen abstractions.},
	keywords = {4-PENTEN-1-OXYL RADICALS, ALKOXY RADICALS, CHEMISTRY, GENERATION, ORGANIC-SYNTHESIS, REDUCING AGENT, RING-CLOSURE REACTIONS, SELECTIVITY, STEREOSELECTIVE-SYNTHESIS, TETRAHYDROFURANS},
	isbn = {1523-7060},
	url = {<Go to ISI>://000260534500094},
	author = {Zlotorzynska, M. and Zhai, H. and Sammis, G. M.}
}
@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 {2107,
	title = {Synthetic studies toward halichlorine: Complex azaspirocycle formation with use of an NBS-promoted semipinacol reaction},
	journal = {Journal of Organic Chemistry},
	volume = {73},
	number = {11},
	year = {2008},
	note = {ISI Document Delivery No.: 307MRTimes Cited: 13Cited Reference Count: 90Hurley, Paul B. Dake, Gregory R.},
	month = {Jun},
	pages = {4131-4138},
	type = {Article},
	abstract = {The investigations of a synthetic route incorporating a NIBS-promoted semipinacol rearrangement to the 6-azaspiro[4.5]decane fragment within halichlorine (1) are presented. A convergent approach was pursued, utilizing two chiral, enantiomerically enriched building blocks, 2-trimethylstannyl piperidene 10 and substituted cyclobutanone 19. Noteworthy synthetic operations in this study include the following: (a) a highly diastereoselective NBS-promoted semipinacol reaction that established four stereogenic centers in ketone 25 and (b) the use of a N-p-toluenesulfonyl-2-iodo-2-piperidene as a precursor to a basic organometallic reagent, which was critical to the success of the coupling of fragments 10 and 19.},
	keywords = {(+/-)-PINNAIC ACID, ASYMMETRIC-SYNTHESIS, BAEYER-VILLIGER OXIDATION, CARBOXYLIC-ACIDS, CRIEGEE REARRANGEMENT, ETHYLMAGNESIUM BROMIDE, ORGANIC-SYNTHESIS, PINNAIC ACID, RING-CLOSING METATHESIS, SPIROCYCLIC CORE},
	isbn = {0022-3263},
	url = {<Go to ISI>://000256323500018},
	author = {Hurley, P. B. and Dake, G. R.}
}
@article {1615,
	title = {Studies toward soraphen A: An aldol-metathesis avenue to the macrocyclic framework},
	journal = {Organic Letters},
	volume = {8},
	number = {13},
	year = {2006},
	note = {ISI Document Delivery No.: 053DITimes Cited: 5Cited Reference Count: 63Vincent, Guillaume Mansfield, Darren J. Vors, Jean-Pierre Ciufolini, Marco A.},
	month = {Jun},
	pages = {2791-2794},
	type = {Article},
	abstract = {We describe a convergent approach to soraphen A, 1, that involves coupling of two fragments by an aldol condensation - olefin metathesis sequence. This route permits rapid access to congeners of 1.},
	keywords = {ALPHA-HYDROXYALLYLATION, ANTIFUNGAL, CARBONYL-COMPOUNDS, CHIRAL ALDEHYDES, ENANTIOSELECTIVE SYNTHESIS, GLIDING BACTERIA, MACROLIDE, OLEFIN METATHESIS, ORGANIC-SYNTHESIS, SILYL ETHERS, STEREOSELECTIVE SYNTHESIS},
	isbn = {1523-7060},
	url = {<Go to ISI>://000238284500034},
	author = {Vincent, G. and Mansfield, D. J. and Vors, J. P. and Ciufolini,Marco A.}
}
@article {811,
	title = {1,4-hydroxybiradical behavior revealed through crystal structure - Solid-state reactivity correlations},
	journal = {Journal of the American Chemical Society},
	volume = {126},
	number = {11},
	year = {2004},
	note = {ISI Document Delivery No.: 804GETimes Cited: 21Cited Reference Count: 27},
	month = {Mar},
	pages = {3511-3520},
	type = {Article},
	abstract = {Structure- reactivity correlations for triplet 1,4-hydroxybiradicals in solution are made difficult by the presence of multiple reactive conformers and the possibility of conformation-dependent intersystem crossing. These problems can be overcome by working in the crystalline state, where the conformations of the 1,4-hydroxybiradicals are fixed and determinable by X-ray crystallography of the parent ketones, assuming that hydrogen atom abstraction occurs with little or no change in conformation. This approach is applied to 15 bi- and tricyclic ketones designed to have slightly different biradical conformations, so that the effect of small and incremental changes in geometry on biradical behaviour can be tested. The results indicate that, while geometry does have a strong influence on 1,4-hydroxybiradical partitioning between cyclization, cleavage, and reverse hydrogen transfer, a full understanding of the results requires that the strain involved in forming the cyclization products be taken into account.},
	keywords = {4-BIRADICALS, BIRADICALS, CONFORMATIONAL MEMORY, GEOMETRIC REQUIREMENTS, II REACTION, ORGANIC-SYNTHESIS, PHENYL KETONES, PHOTOCHEMISTRY, PHOTOCYCLIZATION, STEREOSELECTIVITY, TRIPLET 1},
	isbn = {0002-7863},
	url = {<Go to ISI>://000220286400046},
	author = {Braga, D. and Chen, S. and Filson, H. and Maini, L. and Netherton, M. R. and Patrick, B. O. and Scheffer, J. R. and Scott, C. and Xia, W. J.}
}
@article {829,
	title = {Investigations of alpha-siloxy-epoxide ring expansions forming 1-azaspirocyclic ketones},
	journal = {Journal of Organic Chemistry},
	volume = {69},
	number = {17},
	year = {2004},
	note = {ISI Document Delivery No.: 845XHTimes Cited: 13Cited Reference Count: 97},
	month = {Aug},
	pages = {5676-5683},
	type = {Article},
	abstract = {The construction of 1-azaspirocyclic cycloalkanones using a siloxy-epoxide semipinacol ring expansion process was examined. Functionalized 1-azaspiro[5.5]undecan-7-ones (1-azaspirocyclic cyclohexanones) proceeded in high chemical yields with complete diastereoselectivity using titanium tetrachloride as the Lewis acid promoter. The formation of functionalized 6-azaspiro[5.4]-decan-1-ones (1-azaspirocyclic cyclopentanones) proceeded in high chemical yield with little diastereoselectivity. Modification of reaction parameters such as the Lewis acid promoter or the nature of the silyl ether allowed for the preferential formation of either ("anti" or "syn" 1,2 alkyl shift) diastereomeric product. An explanation for the different reactivity profiles between the cyclobutanol silyl ethers and cyclopentanol silyl ethers is provided.},
	keywords = {1ST TOTAL-SYNTHESIS, ALDOL ALDOL PROCESS, ASYMMETRIC-SYNTHESIS, BAEYER-VILLIGER OXIDATION, LEWIS-ACIDS, ORGANIC-SYNTHESIS, PRACTICAL, QUATERNARY CARBON CENTERS, REARRANGEMENT, SEMI-PINACOL, SILYL ETHER REARRANGEMENTS, STEREOSELECTIVE CONSTRUCTION},
	isbn = {0022-3263},
	url = {<Go to ISI>://000223278200021},
	author = {Dake, G. R. and Fenster, M. D. B. and Fleury, M. and Patrick, B. O.}
}
@article {876,
	title = {Pt(II) or Ag(I) salt catalyzed cycloisomerizations and tandem cycloadditions forming functionalized azacyclic arrays},
	journal = {Organic Letters},
	volume = {6},
	number = {26},
	year = {2004},
	note = {ISI Document Delivery No.: 880TNTimes Cited: 47Cited Reference Count: 41},
	month = {Dec},
	pages = {5023-5026},
	type = {Article},
	abstract = {Cyclic ene-N-p-toluenesulfonamides tethered to an electron-deficient alkyne undergo cycloisomerizations readily under the influence of catalytic Pt(II) salts (PtCl2 or [dppbPtmu-OH](2)(BF4)(2)) or AgOTf. Yields for this process range from 47\% to 99\%. The resulting functionalized 2-azahydrindans can be reacted further using the Diels-Alder reaction. Tandem cycloisomerization-cycloaddition reactions in one pot generate highly functionalized 1-azadecalin ring systems in a highly stereocontrolled manner.},
	keywords = {COMPLEXES, cyclizations, ENAMIDES, ENANTIOSELECTIVE REACTIONS, ENYNES, ORGANIC-SYNTHESIS, palladium, platinum, REORGANIZATION, SKELETAL, STEREOCONTROLLED TOTAL-SYNTHESIS},
	isbn = {1523-7060},
	url = {<Go to ISI>://000225812300057},
	author = {Harrison, T. J. and Dake, G. R.}
}
@article {4517,
	title = {Hydrocarbon C-H bond activation by a tungsten acetylene complex},
	journal = {Organometallics},
	volume = {18},
	number = {17},
	year = {1999},
	note = {ISI Document Delivery No.: 230KBTimes Cited: 13Cited Reference Count: 60},
	month = {Aug},
	pages = {3414-3428},
	type = {Article},
	abstract = {Thermal activation of Cp*W(NO)(eta(2)-CPhCH2)(CH2SiMe3) (1) in neat hydrocarbon solutions transiently generates Cp*W(NO)(eta(2)-PhC=CH) (A), which subsequently activates solvent C-H bonds. For example, the thermolysis of 1 in benzene solution generates quantitatively Cp*W(NO)(eta(2)-CPhCH2)(Ph) (2) The thermolysis of 1 in solutions of methyl-substituted arenes such as toluene or p-, m-, or o-xylene provides mixtures of aryl and benzyl vinyl complexes of the general formulas Cp*W(NO)(eta(2)-CPhCH2)(aryl), Cp*W(NO)(eta(2)-CPhCH2)(eta(1)-benzyl), or Cp*W(NO)(eta(2)-benzyl)(eta(1)-CPh=CH2). Similarly, the thermolysis of 1 in (Me3Si)(2)O affords Cp*W(NO)(eta(2)-CPhCH2)(CH2SiMe2OSiMe3) (10). Mechanistic and kinetic studies support the proposal that the formation of A from 1 by elimination of silane is the rate-controlling process in these reactions. Intra- and intermolecular selectivity studies reveal that the strongest C-H bond (yielding the stronger M-C bond) is the preferred site of reactivity, as expected. Dual C-H bond activation of aliphatic hydrocarbons occurs during the thermal activation ;of I in solutions of these substrates. Consequently, metallacycles of the form Cp*W(NO)(eta(2)-CH(eta(2)-Ph)CH2CH(R)CH2) [(11)R = Pr-n; (12)R = Bu-n; (13)R = Bu-t; and (14)R = OEt] result from the dehydrogenation of n-pentane, n-hexane, 2,2-dimethylbutane, and diethyl ether, respectively. This dual C-H activation process displays a selectivity for substrates that contain an ethyl substituent. Dual C-H bond activation of 2,3-dimethyl-2-butene in the presence of 1 under thermolysis conditions regioselectively affords Cp*W(NO)(eta(3)-endo-CH2C(Me)C(Me)CH2(eta(1)-CPhMe)) (15), Attempts to trap acetylene complex A with PNMe3 result in the formation of the metallacyclopropane complex Cp*W(NO)(CH2SiMe3)(eta(2)-CH2CPh(PMe3)) (16). All new complexes have been characterized by conventional spectroscopic methods, and the solid-state molecular structures of compounds 11, 15, and 16 have been established by X-ray diffraction methods.},
	keywords = {ELIMINATION, HYDROGEN-TRANSFER, ISOMERIZATION, LIGAND, METAL-COMPLEXES, MOLECULAR-STRUCTURE, ORGANIC-SYNTHESIS, ORGANOMETALLIC NITROSYL CHEMISTRY, OXIDATIVE ADDITION, REDUCTIVE, R{\textquoteright} =},
	isbn = {0276-7333},
	url = {<Go to ISI>://000082249400023},
	author = {Debad, D. and Legzdins,Peter and Lumb, S. A. and Rettig, S. J. and Batchelor, R. J. and Einstein, F. W. B.}
}
@article {4298,
	title = {Epimerization via carbon-carbon bond cleavage. L-ribulose-5-phosphate 4-epimerase as a masked class II aldolase},
	journal = {Biochemistry},
	volume = {37},
	number = {16},
	year = {1998},
	note = {ISI Document Delivery No.: ZM208Times Cited: 32Cited Reference Count: 35},
	month = {Apr},
	pages = {5746-5754},
	type = {Article},
	abstract = {Studies indicating that the E. coli L-ribulose-5-phosphate 4-epimerase employs an "aldolase-like" mechanism are reported. This NAD(+)-independent enzyme epimerizes a steseocenter that does not bear an acidic proton and therefore it cannot utilize a simple deprotonation-reprotonation mechanism. Sequence similarities between the epimerase and the class II L-fuculose-1-phosphate aldolase suggest that the two may be evolutionarily related and that the epimerization may occur via carbon-carbon bond cleavage and re-formation. Conserved residues thought to provide the metal ion ligands of the epimerase have been modified using site-directed mutagenesis. The resulting mutants show low k(cat) values in addition to a reduced affinity for Zn2+. These observations serve to establish that there is a structural link between between the active site geometry of the epimerase and the aldolase. In addition, the H97N mutant was found to catalyze the condensation of dihydroxyacetone and glycolaldehyde phosphate to produce a mixture of L-ribulose-5-phosphate and D-xylulose-5-phosphate. This observation of aldolase activity establishes that the epimerase active site is capable of promoting carbon-carbon bond cleavage. Furthermore, glycolaldehyde phosphate was shown to be a competitive inhibitor of the mutant enzyme (K-t = 0.37 mM) but not of the wild-type enzyme. The mutation apparently causes the epimerase to become "leaky" and enables it to bind/generate the normal reaction intermediates from the unbound aldol cleavage products.},
	keywords = {ENZYMES, ESCHERICHIA-COLI, L-FUCULOSE-1-PHOSPHATE ALDOLASE, MECHANISM, MUTAGENESIS, ORGANIC-SYNTHESIS, PCR, PURIFICATION, SEQUENCE, SITE},
	isbn = {0006-2960},
	url = {<Go to ISI>://000073515500048},
	author = {Johnson, A. E. and Tanner, M. E.}
}
@article {4325,
	title = {Ligand elaboration mediated by a Cp*W(NO) template: Stepwise incorporation of small molecules into a tungsten vinyl fragment},
	journal = {Organometallics},
	volume = {17},
	number = {5},
	year = {1998},
	note = {ISI Document Delivery No.: ZC012Times Cited: 21Cited Reference Count: 81},
	month = {Mar},
	pages = {854-871},
	type = {Article},
	abstract = {{Thermolysis of the alkyl vinyl complex Cp*W(NO)(CH2SiMe3)(CPh=CH2) (1) in the presence of unsaturated, heteroatom-containing compounds such as esters and nitriles quantitatively affords metallacyclic products of reductive coupling. These are trapped as 18e complexes via either intramolecular rearrangement or intermolecular reaction with added trapping reagents. The nature of these metallacycles is consistent with the intermediacy of the acetylene complex Cp*W(NO)(eta(2)-CPh=CH) (A) derived in situ from the reductive elimination of SiMe4 from 1. With esters ROAc (R = Me, Et), reductive coupling and C-O bond cleavage yields the alkoxide-containing oxametallacyclopentadiene complexes Cp*W-(No)(eta(2)-O=C(Me)CH=CPh)(OR) (2},
	keywords = {ACTIVATION, ALKYNE COMPLEXES, BOND-CLEAVAGE, C-H, INSERTION, KETONE COMPLEXES, METAL-COMPLEXES, ORGANIC-SYNTHESIS, ORGANOMETALLIC NITROSYL CHEMISTRY, RAY CRYSTAL-STRUCTURE, SEQUENTIAL, ZIRCONOCENE COMPLEXES},
	isbn = {0276-7333},
	url = {<Go to ISI>://000072530700014},
	author = {Legzdins,Peter and Lumb, S. A. and Young, V. G.}
}
@article {4395,
	title = {UDP-N-trifluoroacetylglucosamine as an alternative substrate in N-acetylglucosaminyltransferase reactions},
	journal = {Carbohydrate Research},
	volume = {306},
	number = {1-2},
	year = {1998},
	note = {ISI Document Delivery No.: 100VZTimes Cited: 15Cited Reference Count: 28},
	month = {Jan},
	pages = {127-136},
	type = {Article},
	abstract = {The synthesis of UDP-N-trifluoroacetylglucosamine [uridine 5{\textquoteright}-(2-trifluoroacetamido-2-deoxy-alpha-D-glucopyranosyl diphosphate, UDP-GlcNAc-F-3] is reported. The compound is found to serve as a substrate for the {\textquoteright}core-2{\textquoteright} GlcNAc transferase (EC 2.4.1.102) that is involved in the biosynthesis, of O-linked glycoproteins and for the GlcNAcT-V transferase (EC 2.4. 1.155) that is a key biosynthetic enzyme controlling the branching pattern of cell surface complex Asn-linked oligosaccharides. The trisaccharide beta-o-Gal p-(1 {\textendash}> 3)-[beta-D-GlcpNAc-F-3(1 {\textendash}> 6)]alpha-D-GalpNAc-OR [R = (CH2)(8)CO2Me] was prepared from beta-D-Galp-(1 {\textendash}> 3)-alpha-D-GalpNAc-OR using the {\textquoteright}core-2{\textquoteright} GlcNAc transferase. The tetrasaccharide beta-D-GlcpNAc-(1 {\textendash}> 2)-[beta-D-GlcpNAc-F-3-(1 {\textendash}> 6)]-alpha-D-Manp-(1 {\textendash}> 6)-beta-D-Glcp-OR [R = (CH2)(7)CH3] was prepared from beta-D-GlcpNAc-(1 {\textendash}> 2)-alpha-D-Manp-(1 {\textendash}> 6)-beta-D-Glcp-OR [R = (CH2)(7)CH3] using the GlcNAcT-V transferase. Removal of the trifluoroacetyl group was achieved under mild basic conditions to give the corresponding glucosamine containing tetrasaccharide. These examples demonstrate the feasibility of introducing masked forms of glucosamine residues into oligosaccharides using GlcNAc-specific transferases. The requirement for the trifluoroacetamido group as a specific recognition element was evident in the observation that neither UDP-glucosamine nor UDP-glucose served as a donor substrates for the {\textquoteright}core-2{\textquoteright} GlcNAc transferase. (C) 1998 Elsevier Science Ltd. All rights reserved.},
	keywords = {GLYCOPROTEINS, N-acetylglucosaminyltransferase, OLIGOSACCHARIDE, OLIGOSACCHARIDES, ORGANIC-SYNTHESIS, RECOGNITION, SYNTHESIS, UDP-sugar analog},
	isbn = {0008-6215},
	url = {<Go to ISI>://000074837200012},
	author = {Sala, R. F. and MacKinnon, S. L. and Palcic, M. M. and Tanner, M. E.}
}
@article {3663,
	title = {A remarkable multiple rearrangement process in the bromination of endo-3-bromo-4-methylcamphor: Intermediates for triterpenoid synthesis},
	journal = {Tetrahedron},
	volume = {52},
	number = {47},
	year = {1996},
	note = {ISI Document Delivery No.: VT272Times Cited: 2Cited Reference Count: 36},
	month = {Nov},
	pages = {14661-14672},
	type = {Article},
	abstract = {The remarkable transformation of endo-3-bromo-4-methylcamphor (9) to endo-3,9-dibromo-4-(bromomethyl)camphor (11) forms the basis of a new approach to intermediates for the synthesis of lanostane triterpenoids, euphane triterpenoids and 14 alpha-methyl steroids. Copyright (C) 1996 Elsevier Science Ltd},
	keywords = {4-METHYLCAMPHOR, CAMPHOR, CYCLIZATION, DERIVATIVES, ENANTIOSPECIFIC SYNTHESIS, NATURAL PRODUCT SYNTHESIS, ORGANIC-SYNTHESIS, ROUTE, STEROID-SYNTHESIS, SYNTHONS},
	isbn = {0040-4020},
	url = {<Go to ISI>://A1996VT27200003},
	author = {Ferguson, C. G. and Money, T. and Pontillo, J. and Whitelaw, P. D. M. and Wong, M. K. C.}
}
@article {7012,
	title = {PREPARATION AND ISOMERIZATION OF 1-PHENYLSELENO 1,3-DIENES},
	journal = {Journal of Organic Chemistry},
	volume = {56},
	number = {26},
	year = {1991},
	note = {ISI Document Delivery No.: GW891Times Cited: 18Cited Reference Count: 33},
	month = {Dec},
	pages = {7201-7211},
	type = {Article},
	abstract = {{The preparation of a series of 1-phenylseleno 1,3-dienes is described starting from enyne derivatives via a hydrozirconation/transfer sequence. Hydrozirconation of a series of conjugated enynes having the general formula HC = CCR1 = CR2R3 (3a: R1 = R2 = R3 = H; 3b: R1 = R3 = H},
	keywords = {CONVENIENT PREPARATION, DERIVATIVES, DIELS-ALDER REACTIONS, HYDROZIRCONATION, ORGANIC-SYNTHESIS, ORGANOSELENIUM CHEMISTRY, selenium, TRANSITION-METAL DIENYLS, transmetalation, ZIRCONIUM},
	isbn = {0022-3263},
	url = {<Go to ISI>://A1991GW89100006},
	author = {Fryzuk,Michael D. and Bates, G. S. and Stone, C.}
}
@article {7036,
	title = {STEREOSELECTIVITY OF C(3) METHYLATION AND ALDOL CONDENSATION OF CAMPHOR AND DERIVATIVES},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {69},
	number = {3},
	year = {1991},
	note = {ISI Document Delivery No.: FE808Times Cited: 14Cited Reference Count: 38},
	month = {Mar},
	pages = {558-566},
	type = {Article},
	abstract = {The stereoselectivity of methylation and aldol condensation of camphor and derivatives is determined by the presence or absence of a C(7) syn-methyl group and (or) C(5) and C(6) endo-hydrogen atoms.},
	keywords = {APPROACH, BICYCLO<2.2.1>HEPTANES, C(3)ALDOL, C(3)METHYLATION, CAMPHOR, NUCLEAR MAGNETIC-RESONANCE, ORGANIC-SYNTHESIS, PSEUDOGUAIANOLIDES, STEREOCONTROLLED, VITAMIN-D METABOLITES},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1991FE80800029},
	author = {Hutchinson, J. H. and Li, D. L. F. and Money, T. and Palme, M. and Agharahimi, M. R. and Albizati, K. F.}
}
