All-cis-[5.5.5.5]Fenestran = [5.5.5.5] Fenestrane tout-cis = All-cis-[5.5.5.5] FenestraneLUYTEN, M; KEESE, R.Angewandte Chemie. 1984, Vol 96, Num 5, pp 358-359, issn 0044-8249Article

Investigating the Arenyl-Diene Double [3 + 2] Photocycloaddition ReactionPENKETT, Clive S; WOOLFORD, Jason A; READ, Timothy W et al.Journal of organic chemistry. 2011, Vol 76, Num 5, pp 1295-1304, issn 0022-3263, 10 p.Article

The quest for planarizing distortions in hydrocarbons: two stereoisomeric [4.5.5.5]fenestranesTHOMMEN, Marc; PREVOT, Lionel; EBERLE, Marcel K et al.Tetrahedron (Oxford. Print). 2011, Vol 67, Num 21, issn 0040-4020, 3766, 3868-3873 [7 p.]Article

SYNTHETIC APPROACHES TO PLANAR CARBON. ITEN HOEVE W; WYNBERG H.1980; J. ORG. CHEM.; USA; DA. 1980; VOL. 45; NO 15; PP. 2925-2930; BIBL. 25 REF.Article

THE FIRST P^V-P^V COMPOUND: BIS (CYCLENPHOSPHORANE), (C₈H₁₆N₄P)₂RICHMAN JE; DAY RO; HOLMES RR et al.1981; INORG. CHEM.; ISSN 0020-1669; USA; DA. 1981; VOL. 20; NO 10; PP. 3378-3381; BIBL. 16 REF.Article

Planarisierung von tetrakoordinierten Kohlenstoffatom. Synthese des überbrückten all-cis-[5.5.5.5]Fenestrans 13-Oxapentacyclo[5.5.2.1^1,7.0^4,15.0^10,15]pentadecan-14-on = Planarisation de l'atome de carbone tétracoordiné. Synthèse du [5.5.5.5] fenestrane ponté tout-cis: Oxa-13 pentacyclo [5.5.2.1^1,7.0.^4,5.0^10,15] pentadécanone-14 = Planarisation of tetracoordinate carbon atom. Synthesis of the bridged all-cis-[5.5.5.5] fenestrane: 13-oxapentacyclo [5.5.2.1^1.7.0^4.15.0^10.15] pentadecan-14onePFENNINGER, A; ROESLE, A; KEESE, R et al.Helvetica chimica acta. 1985, Vol 68, Num 2, pp 493-507, issn 0018-019XArticle

SYNTHESIS OF (4.5.5.5) FENESTRANE AND A (4.4.5.5) FENESTRANE DERIVATIVEDAUBEN WG; WALKER DM.1982; TETRAHEDRON LETT.; ISSN 0040-4039; GBR; DA. 1982; VOL. 23; NO 7; PP. 711-714; BIBL. 14 REF.Article

Planarisation of tetracoordinate carbon atom. A further route to (all-cis)-[5.5.5.5]fenestraneLUYTEN, M; KEESE, R.Helvetica chimica acta. 1984, Vol 67, Num 8, pp 2242-2245, issn 0018-019XArticle

THE (4.4.4.4) FENESTRANES AND (2.2.2.2.) PADDLANE. PROSPECTS FOR THE REALIZATION OF PLANAR TETRACOORDINATE CARBON.WURTHWEIN EU; JAYARAMAN CHANDRASEKHAR; JEMMIS ED et al.1981; TETRAHEDRON LETT.; ISSN 0040-4039; GBR; DA. 1981; VOL. 22; NO 9; PP. 843-846; BIBL. 9 REF.Article

Synthesis and electron-diffraction structure of all-cis-[5.5.5.5]fenestraneBRUNVOLL, J; GUIDETTI-GREPT, R; HARGITTAI, I et al.Helvetica chimica acta. 1993, Vol 76, Num 8, pp 2838-2846, issn 0018-019XArticle

Angular distortions at tetracoordinate carbon: planoid configurations in substituted spiro[4.4]nonanesLUEF, W; KEESE, R; BÜRGI, H.-B et al.Helvetica chimica acta. 1987, Vol 70, Num 3, pp 534-542, issn 0018-019XArticle

Total synthesis of (±)-lauren-1-ene, the unique fenestrane diterpeneTSUNODA, T; AMAIKE, M; TAMBUNAN, U. S. F et al.Tetrahedron letters. 1987, Vol 28, Num 22, pp 2537-2540, issn 0040-4039Article

Intramolecular photocycloadditions: synthesis of sterically congested substituted [4.5.5.5] fenestranes. Models for the total synthesis of laurenene and silphineneCRIMMINS, M. T; MASCARELLA, S. W; BREDON, L. D et al.Tetrahedron letters. 1985, Vol 26, Num 8, pp 997-1000, issn 0040-4039Article

A cis,trans,cis,cis-[4.5.5.5]fenestrane derivativeTHOMMEN, M; KEESE, R; FÖRTSCH, M et al.Acta crystallographica. Section C, Crystal structure communications. 1996, Vol 52, pp 2051-2053, issn 0108-2701, 8Article

General approach for the synthesis of polyquinenes via the Weiss reaction. XV: Synthesis of the [5.5.5.5]fenestrane system via the aldol approach and studies directed toward the [5.5.6.6]fenestranesXIAOYONG FU; KUBIAK, G; WEIJIANG ZHANG et al.Tetrahedron (Oxford. Print). 1993, Vol 49, Num 8, pp 1511-1524, issn 0040-4020Article

General approach for the synthesis of polyquiness via the weiss reaction XIII. Aldol approach to fenestranesKUBIAK, G; FU, X; GUPTA, A. K et al.Tetrahedron letters. 1990, Vol 31, Num 30, pp 4285-4288, issn 0040-4039, 4 p.Article

Synthetic studies on arene―olefin cycloadditions. X: A concise, stereocontrolled total synthesis of (±)-laureneneWENDER, P. A; VON GELDERN, T. W; LEVINE, B. H et al.Journal of the American Chemical Society. 1988, Vol 110, Num 14, pp 4858-4860, issn 0002-7863Article

Some thermal and photochemical reactions of [4.4.4.5]fenestranesWOLFF, S; VENEPALLI, B. R; GEORGE, C. F et al.Journal of the American Chemical Society. 1988, Vol 110, Num 20, pp 6785-6790, issn 0002-7863Article

Planoid distortions in bridged spirocompounds: formation of (all-cis)-[5.5.5.5]fenestrane in the attempted synthesis of the (cis,cis,cis,trans)-isomerLUYTEN, M; KEESE, R.Tetrahedron (Oxford. Print). 1986, Vol 42, Num 6, pp 1687-1691, issn 0040-4020Article

5-TETRACYCLO (3.3.0.0^2.40^3.6) OCT-7-ENYL CARBENE; AN ATTEMPTED SYNTHESIS OF A (4.4.4.4) FENESTRANE DERIVATIVESTAPERSMA J; ROOD IDC; KLUMPP GW et al.1982; TETRAHEDRON; ISSN 0040-4020; GBR; DA. 1982; VOL. 38; NO 20; PP. 3051-3058; BIBL. 33 REF.Article

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Cation, carbene, and radical centers in a [4.4.4.5]fenestraneVENUGOPAL, D; AGOSTA, W. C.Tetrahedron (Oxford. Print). 1992, Vol 48, Num 33, pp 6757-6762, issn 0040-4020Article

A transannulation route to the [5.5.5.7]fenestrane ring system of laureneneGOVERDHAN MEHTA; KASIBHATLA SRINIVAS RAO.Journal of organic chemistry. 1988, Vol 53, Num 2, pp 425-427, issn 0022-3263Article

A SHORT SYNTHESIS OF TRICYCLO (4.2.0.0^1,4) OCTANESWOLFF S; AGOSTA WC.1981; J. ORG. CHEM.; ISSN 0022-3263; USA; DA. 1981; VOL. 46; NO 24; PP. 4821-4825; BIBL. 24 REF.Article

Sequential actions of cobalt nanoparticles and palladium(II) catalysts: Three-step one-pot synthesis of fenestranes from an enyne and an alkyne diesterSEUNG UK SON; KANG HYUN PARK; YOUNG KEUN CHUNG et al.Journal of the American Chemical Society. 2002, Vol 124, Num 24, pp 6838-6839, issn 0002-7863Article