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PROPELLANES. XV. SYNTHESIS OF 3-THIA (3.2.2.) PROPELLANE AND ATTEMPTED RING CONTRACTION OF 5-MEMBERED THIOETHER RINGS TO CYCLOBUTANESLANTOS I; GINSBURG D.1972; TETRAHEDRON; G.B.; DA. 1972; VOL. 28; NO 9; PP. 2507-2519; BIBL. 24 REF.Serial Issue

PROPELLANES. VIII. SOME BENT CYCLOPROPYL CATIONS-ARE THEY PARTIALLY-OPENED.WARNER P; SHIH LAI LU; SUAE CHEN CHANG et al.1978; TETRAHEDRON LETTERS; G.B.; DA. 1978; NO 22; PP. 1947-1950; BIBL. 17 REF.Article

GENERAL METHOD FOR THE SYNTHESIS OF (N.3.3) PROPELLANES, N >OU= 3.WEBER RW; COOK JM.1978; CANAD. J. CHEM.; CANADA; DA. 1978; VOL. 56; NO 2; PP. 189-192; ABS. FR.; BIBL. 11 REF.Article

(2.2.1) PROPELLANEWALKER FH; WIBERG KB; MICHL J et al.1982; J. AM. CHEM. SOC.; ISSN 0002-7863; USA; DA. 1982; VOL. 104; NO 7; PP. 2056-2057; BIBL. 29 REF.Article

Synthesis of monosubstituted [1.1.1]propellanesBOTHE, H; SCHLUÊTER, A.-D.Chemische Berichte. 1991, Vol 124, Num 3, pp 587-590, issn 0009-2940, 4 p.Article

PHOTOELECTRON SPECTRA OF DITHIAPROPELLANESKOBAYASHI M; GLEITER R.1978; Z. NATURFORSCH., B; DEU; DA. 1978; VOL. 33; NO 9; PP. 1057-1058; BIBL. 4 REF.Article

REACTIONS OVER SUPPORTED METAL CATALYSTS. IV. THE STEREOCHEMISTRY AND MECHANISM OF HYDROGENOLYSIS OF SOME PROPELLANES.GOODING KR; JACKSON WR; PINCOMBE CF et al.1977; AUSTRAL. J. CHEM.; AUSTRAL.; DA. 1977; VOL. 30; NO 7; PP. 1517-1522; BIBL. 10 REF.Article

KONSTITUTIONS- UND KONFIGURATIONSAUFKLAERUNG DER ISOMEREN DICHLORDITHIAPROPELLANTETROXIDE MIT HILFE DER ¹³C-NMR-SPEKTROSKOPIE. = CONSTITUTION ET CONFIGURATION DE DICHLORODITHIAPROPELLANES TETRAOXYDE ISOMERES A L'AIDE DE LA SPECTROMETRIE RMN DE ¹³CWEINGES K; BAAKG H; DISTLER H et al.1977; CHEM. BER.; DTSCH.; DA. 1977; VOL. 110; NO 9; PP. 2978-2985; ABS. ANGL.; BIBL. 8 REF.Article

PROPELLANES. I: 3,6,10,13-TETRATHIA(4,5,11,12-TRANS-DICYCLOHEXANO)-(6,6,1) PROPELLANE = PROPELLANES. I: TETRATHIA-3,6,10,13(TRANS-DICYCLOHEXANO-4,5,11,12) (6.6.1) PROPELLANEJAMROZIK J.1979; J. PRAKT. CHEM.; DDR; DA. 1979; VOL. 321; NO 3; PP. 437-442; ABS. GER; BIBL. 10 REF.Article

Deprotonation of hydrazinium dications in the diazoniapropellane series to form bridgehead iminium ions; external and intramolecular trappingALDER, R. W; SESSIONS, R. B; GMUNDER, J. O et al.Perkin transactions. 2. 1984, Num 3, pp 411-417, issn 0300-9580Article

(1.1.1.) PROPELLANEWIBERG KB; WALKER FH.1982; J. AM. CHEM. SOC.; ISSN 0002-7863; USA; DA. 1982; VOL. 104; NO 19; PP. 5239-5240; BIBL. 17 REF.Article

Synthesis of bicyclo[n.2.1] bridgehead alkenes acetoxy substituted at the opposite bridgehead positionTOBE, Y; FUKUDA, Y; KAKIUCHI, K et al.Journal of organic chemistry. 1984, Vol 49, Num 11, pp 2012-2015, issn 0022-3263Article

High molecular weight poly([1.1.1]propellane)s and a new polyamide with bicyclo[1.1.1]pentane fragmentsBOTHE, H; SCHLÜTER, A.-D.Advanced materials (Weinheim). 1991, Vol 3, Num 9, pp 440-442, issn 0935-9648Article

ERGIEBIGE SYNTHESE VON HEPTALEN AUS NAPHTHALIN UEBER EIN BIS(BICYCLO (1.1.0) BUTAN)-DERIVAT = SYNTHESE EXCELLENTE D'HEPTALENE A PARTIR DE NAPHTALENE EN PASSANT PAR UN DERIVE DU BIS(BICYCLO(1.1.0) BUTANE)PAQUETTE LA; BROWNE AR; CHAMOT E et al.1979; ANGEW. CHEM.; DEU; DA. 1979; VOL. 91; NO 7; PP. 581-582; BIBL. 9 REF.Article

REDUCTIVE CLEAVAGE OF PROPELLANE-TYPE HYDRAZINIUM DICATIONS AS A ROUTE TO MEDIUM-SIZED RING BICYCLIC DIAMINES WITH BRIDGEHEAD NITROGEN ATOMSALDER RW; SESSIONS RB; BENNET AJ et al.1982; PERKIN TRANS. 1; ISSN 0300-922X; GBR; DA. 1982; NO 2; PP. 603-609; BIBL. 18 REF.Article

Synthesis of a potential bifunctional mimic of transaminasesYIKANG WU; AHLBERG, P.Acta chemica scandinavica (Copenhagen. 1989). 1992, Vol 46, Num 1, pp 60-72, issn 0904-213XArticle

Propellanes. LXXIII: Cyclic oligomers from a [4.3.3] propellene-bis-imide and 1,ω-dibromoalkanesASHKENAZI, P; TATARSKY, D; GINSBURG, D et al.Tetrahedron (Oxford. Print). 1984, Vol 40, Num 17, pp 3325-3328, issn 0040-4020Article

PROPELLANES AS STEREOCHEMICAL MODELSGINSBURG D.1974; ACCOUNTS CHEM. RES.; U.S.A.; DA. 1974; VOL. 7; NO 9; PP. 286-293; BIBL. 19 REF.Article

Die zentrale Propellanbindung als polymerisationsfähige CC-Einfachbindung: Poly(tricyclo[4.2.0.0^2,7]octan-1,7-diyl) ― ein «Poly([1.1.1]propellan)» = La liaison centrale du propellane comme liaison simple CC apte à la polymérisation: (polytricyclo [4.2.0.0^2,7] octandiyl-1,7), un poly [1.1.1] propellane = The central propellan bond as a polymerisable simple CC bond : polytricyclo [4.2.0.0^2,7] octonedyl-1,7 a poly [1.1.1] propellaneSCHLÜTER, A.-D.Angewandte Chemie. 1988, Vol 100, Num 2, pp 283-285, issn 0044-8249Article

A [1.1.1]propellane with a protected functional group in the side chain and its homopolymerFREUDENBERGER, R; LAMER, W; SCHLÜTER, A.-D et al.Journal of organic chemistry. 1993, Vol 58, Num 23, pp 6497-6498, issn 0022-3263Article

8,11-DICHLORO (5) METACYCLOPHANETURKENBURG LAM; DE WOLF WH; BICKELHAUPT F et al.1983; TETRAHEDRON LETTERS; ISSN 0040-4039; GBR; DA. 1983; VOL. 24; NO 17; PP. 1817-1820; BIBL. 13 REF.Article

2,6-METHANO-2,6-DEHYDRONORBORNANE: AN EXCEPTIONALLY STRAINED (3.1.1) PROPELLANEVINKOVIC V; MAJERSKI Z.1982; J. AM. CHEM. SOC.; ISSN 0002-7863; USA; DA. 1982; VOL. 104; NO 14; PP. 4027-4029; BIBL. 24 REF.Article

THERMOLYSIS OF THE (N.2.2) PROPELLANES. MECHANISMS FOR THE THERMOLYSIS OF BICYCLO (2.2.0) HEXANESWIBERG KB; MATTURRO MG.1981; TETRAHEDRON LETT.; ISSN 0040-4039; GBR; DA. 1981; VOL. 22; NO 36; PP. 3481-3484; BIBL. 14 REF.Article

THERMOLYSIS OF THE TRICYCLIC 1,2-DIOXETANES 3,4:3,4-DIPROPANO-3,4-PENTANO-3,4-PROPANO-, AND 3,4-BUTANO-3,4-PROPANO-1,2-DIOXETANEKOPECKY KR; LOCKWOOD PA; GOMEZ RR et al.1981; CAN. J. CHEM.; ISSN 0008-4042; CAN; DA. 1981; VOL. 59; NO 5; PP. 851-858; ABS. FRE; BIBL. 38 REF.Article