ChemInform Abstract: ROUTES TO BICYCLO (X.3.0) RING SYSTEMS: STEREOSELECTIVE SYNTHESIS OF CIS AND TRANS-8-METHYLHYDRINDANS

Chemischer Informationsdienst ◽

10.1002/chin.197937194 ◽

1979 ◽

Vol 10 (37) ◽

Author(s):

P. R. BERNSTEIN ◽

G. STORK

Keyword(s):

Stereoselective Synthesis ◽

Ring Systems ◽

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ChemInform Abstract: (Dichloromethyl)dimethylsilyl Group as a Hydroxymethylidene Diradical Equivalent: Radical Annulation of Dienols and Its Application to the Stereoselective Synthesis of cis- and trans-Hydrindan Ring Systems.

10.1002/chin.199452116 ◽

2010 ◽

Vol 25 (52) ◽

pp. no-no

Author(s):

K. TAMAO ◽

K. NAGATA ◽

Y. ITO ◽

K. MAEDA ◽

M. SHIRO

Keyword(s):

Stereoselective Synthesis ◽

Ring Systems ◽

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Stereoselective Synthesis of cis-and trans-Beta,Gamma-Unsaturated Carboxylic Esters via Reaction of Alkenyldichloroboranes with Ethyl Diazoacetate

10.21236/ada239049 ◽

1991 ◽

Author(s):

Herbert C. Brown ◽

Ashok M. Salunkhe

Keyword(s):

Stereoselective Synthesis ◽

Ethyl Diazoacetate ◽

Carboxylic Esters ◽

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Chiral recognition in the reaction of the enolate derived from [(η5-C5H5)Fe(CO)(PPh3)COCH2OCH2Ph] with cis- and trans-2,3-epoxybutane: The stereoselective synthesis of cis and trans-βγ-disubstituted-γ-lactones

Tetrahedron Letters ◽

10.1016/s0040-4039(00)95262-6 ◽

1989 ◽

Vol 30 (5) ◽

pp. 587-590 ◽

Author(s):

Stephen G. Davies ◽

David Middlemiss ◽

Alan Naylor ◽

Martin Wills

Keyword(s):

Chiral Recognition ◽

Stereoselective Synthesis ◽

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ChemInform Abstract: NICKEL COMPLEX-CATALYSED REACTION OF PROPYLMAGNESIUM BROMIDE WITH BUTADIENE, A HIGHLY STEREOSELECTIVE SYNTHESIS OF CIS- AND TRANS-(2-VINYLCYCLOPENTYL)METHYLMAGNESIUM BROMIDE

Chemischer Informationsdienst ◽

10.1002/chin.197527329 ◽

1975 ◽

Vol 6 (27) ◽

pp. no-no

Author(s):

H. FELKIN ◽

L. D. KWART ◽

G. SWIERCZEWSKI ◽

J. D. UMPLEBY

Keyword(s):

Nickel Complex ◽

Stereoselective Synthesis ◽

Catalysed Reaction ◽

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Rearrangement-Ring Expansion Reaction of Functionalized Cyclic Ethers. Stereoselective Synthesis of the ST- and XY-Ring Systems of Maitotoxin

Heterocycles ◽

10.3987/com-96-s31 ◽

1997 ◽

Vol 44 (1) ◽

pp. 105 ◽

Author(s):

Tadashi Nakata ◽

Kazuo Nagasawa ◽

Nobuyuki Hori ◽

Ryuichi Shiba

Keyword(s):

Stereoselective Synthesis ◽

Ring Expansion ◽

Cyclic Ethers ◽

Ring Systems ◽

Ring Expansion Reaction

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ChemInform Abstract: STRAINED RING SYSTEMS. 16. SUBSTITUENT EFFECTS ON THE PKA VALUES OF CIS- AND TRANS-1,2-DIMETHYL-2-X-CYCLOPROPANE-1-CARBOXYLIC ACIDS AND RELATED BICYCLO(N.1.0)ALKANE-1-CARBOXYLIC ACIDS

Chemischer Informationsdienst ◽

10.1002/chin.197710168 ◽

1977 ◽

Vol 8 (10) ◽

pp. no-no

Author(s):

R. N. MCDONALD ◽

R. R. REITZ

Keyword(s):

Carboxylic Acids ◽

Substituent Effects ◽

Ring Systems ◽

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ChemInform Abstract: SYNTHESIS OF CIS- AND TRANS-ENYNES IN THE CLASS OF 12- AND 15-MEMBERED RING SYSTEMS

Chemischer Informationsdienst ◽

10.1002/chin.198243180 ◽

1982 ◽

Vol 13 (43) ◽

Author(s):

J. ZOUNTSAS ◽

H. MEIER

Keyword(s):

Membered Ring ◽

Ring Systems ◽

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ChemInform Abstract: SYNTHESIS APPLICATIONS OF CATIONIC AZA-COPE REARRANGEMENTS. PART 13. STEREOSELECTIVE SYNTHESIS OF CIS- AND TRANS-3A-ARYL-4-OXODECAHYDROCYCLOHEPTA(B)PYRROLES

Chemischer Informationsdienst ◽

10.1002/chin.198413156 ◽

1984 ◽

Vol 15 (13) ◽

Author(s):

L. E. OVERMAN ◽

E. J. JACOBSEN ◽

R. J. DOEDENS

Keyword(s):

Stereoselective Synthesis ◽

Cope Rearrangements ◽

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ChemInform Abstract: STEREOSELECTIVE SYNTHESIS OF CIS- AND TRANS-2-SUBSTITUTED 1,3-DITHIANE 1-OXIDES

Chemischer Informationsdienst ◽

10.1002/chin.197712231 ◽

1977 ◽

Vol 8 (12) ◽

pp. no-no

Author(s):

F. A. CAREY ◽

O. D. DAILEY ◽

O. HERNANDEZ ◽

J. R. TUCKER

Keyword(s):

Stereoselective Synthesis ◽

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Intramolecular Diels−Alder Reactions of 3-(Tetrahydropyridinyl)indoles: Stereoselective Synthesis of Novel Pentacyclic Ring Systems

The Journal of Organic Chemistry ◽

10.1021/jo971981+ ◽

1998 ◽

Vol 63 (6) ◽

pp. 1974-1980 ◽

Author(s):

Parviz Gharagozloo ◽

Masao Miyauchi ◽

Berry Birdsall ◽

Nigel J. M. Birdsall

Keyword(s):

Stereoselective Synthesis ◽

Diels Alder ◽

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