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Featured researches published by Janet Finer.


Tetrahedron | 1979

Ilimaquinone, a sesquiterpenoid quinone from a marine sponge

Richard T. Luibrand; Timothy R. Erdman; John J. Vollmer; Paul J. Scheuer; Janet Finer; Jon Clardy

Abstract Ilimaquinone (1) is a new sponge metabolite of composition C22H30O4. Its structure, which was determined by spectral correlations and X-ray crystallography, comprises a rearranged drimane sesquiterpene moiety linked to a 2-hydroxy-5-methoxybenzoquinone at C-3.


Phytochemistry | 1977

Diterpenes from Dictyota dichotoma

D. John Faulkner; B. N. Ravi; Janet Finer; Jon Clardy

Two new and two known diterpenes were isolated from Dictyota dichotoma. The structures of the new diterpenes were elucidated from spectral and X-ra


Journal of Organometallic Chemistry | 1976

Synthesis and structure of dicarbonyldi-η-cyclopentadienylbis(μ-thiocarbonyl)diiron, a thiocarbonyl analog of the dicarbonyl-η-cycglopentadienyliron dimer

Jan W. Dunker; Janet Finer; Jon Clardy; Robert J. Angelici

Abstract Sodium hydride reduction of (η-C5H5)Fe(CO)2(CS)+ gives cis- and trans[(η-C5H5)Fe(CS) (CO)]2. The trans isomer slowly converts to a cis—trans mixture in xylene solution. An X-ray structural study of the cis isomer shows the CS groups to be in the bridging positions, but otherwise, its structure is nearly identical to that of cia-[(η-C5H5)Fe(CO)2]2. The cis isomer reacts with CH3OSO2F to give the compound, (η-C5H5)2Fe2(CSCH3)(CS)(CO)2+, with a methylated bridging thiocarbonyl group.


Tetrahedron Letters | 1979

The synthesis and structure of 10,11-bistrifluoromethyl-i,o-bicyclo[7.2.2]trideca-10,12-diene. A highly strained inside-outside bicycloalkane derivative.

Paul G. Gassman; Stewart R. Korn; Thomas F. Bailey; Thomas H. Johnson; Janet Finer; Jon Clardy

Abstract 10,11-Bistrifluoromethyl-i,o-bicyclo[7.2.2]trideca-10,12-diene has been prepared by the Diels-Alder addition of hexafluoro-2-butyne to cis, trans-cycloundeca-1,3-diene. Purification was accomplished via formation of an iron tricarbonyl complex whose structure was established via X-ray crystallography.


Archive | 1977

X-ray Diffraction and the Structure of Marine Natural Products

Janet Finer; K. Hirotsu; Jon Clardy

While the success of X-ray diffraction in the elucidation of molecular structure is well known to natural products chemists, the physical principles responsible for this success appear to be only dimly perceived. Various idiosyncratic views range from disgust at an approach that smacks of cheating to contentment with an expeditious way to secure structures. In spite of this wide range of relatively uninformed views, a single-crystal X-ray analysis is taken as the ultimate measure of molecular structure. Why should this be the case?


Journal of the American Chemical Society | 1975

9-Isocyanopupukeanane, a marine invertebrate allomone with a new sesquiterpene skeleton

B. Jay Burreson; Paul J. Scheuer; Janet Finer; Jon Clardy


Helvetica Chimica Acta | 1979

Defense Allomones of the Nudibranch Phyllidia varicosa Lamarck 1801

Mark R. Hagadone; B. Jay Burreson; Paul J. Scheuer; Janet Finer; Jon Clardy


Journal of Organic Chemistry | 1979

Structures of dictyodial and dictyolactone, unusual marine diterpenoids

Janet Finer; Jon Clardy; William Fenical; L. Minale; Raffaele Riccio; Julian Battaile; Michael P. Kirkup; Richard E. Moore


Journal of the American Chemical Society | 1976

A NOVEL DITERPENE FROM DOLLABELLA CALIFORNICA

Chris M. Ireland; D. J. Faulkner; Janet Finer; Jon Clardy


Journal of Organic Chemistry | 1976

Some chemical constituents of the digestive gland of the sea hare Aplysia californica.

Chris M. Ireland; Martha O. Stallard; D. John Faulkner; Janet Finer; Jon. Clardy

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Paul J. Scheuer

University of Hawaii at Manoa

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B. Jay Burreson

University of Hawaii at Manoa

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D. J. Faulkner

University of California

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