Vote for your favorite mineral in #MinCup25! - Kosmochlor vs. Azurite
It's a battle of green vs blue as rare but vibrant chromium-bearing kosmochlor up against the deep blue copper alteration mineral azurite.
Log InRegister
Quick Links : The Mindat ManualThe Rock H. Currier Digital LibraryMindat Newsletter [Free Download]
Home PageAbout MindatThe Mindat ManualHistory of MindatCopyright StatusWho We AreContact UsAdvertise on Mindat
Donate to MindatCorporate SponsorshipSponsor a PageSponsored PagesMindat AdvertisersAdvertise on Mindat
Learning CenterWhat is a mineral?The most common minerals on earthInformation for EducatorsMindat ArticlesThe ElementsThe Rock H. Currier Digital LibraryGeologic Time
Minerals by PropertiesMinerals by ChemistryAdvanced Locality SearchRandom MineralRandom LocalitySearch by minIDLocalities Near MeSearch ArticlesSearch GlossaryMore Search Options
Search For:
Mineral Name:
Locality Name:
Keyword(s):
 
The Mindat ManualAdd a New PhotoRate PhotosLocality Edit ReportCoordinate Completion ReportAdd Glossary Item
Mining CompaniesStatisticsUsersMineral MuseumsClubs & OrganizationsMineral Shows & EventsThe Mindat DirectoryDevice SettingsThe Mineral Quiz
Photo SearchPhoto GalleriesSearch by ColorNew Photos TodayNew Photos YesterdayMembers' Photo GalleriesPast Photo of the Day GalleryPhotography

Stork, Gilbert, Cohen, Jonathan F. (1974) Ring size in epoxynitrile cyclization. General synthesis of functionally substituted cyclobutanes. Application to (+-)-grandisol. Journal Of The American Chemical Society, 96 (16) 5270-5272 doi:10.1021/ja00823a053

Advanced
   -   Only viewable:
Reference TypeJournal (article/letter/editorial)
TitleRing size in epoxynitrile cyclization. General synthesis of functionally substituted cyclobutanes. Application to (+-)-grandisol
JournalJournal Of The American Chemical Society
AuthorsStork, GilbertAuthor
Cohen, Jonathan F.Author
Year1974 (August)Volume96
Issue16
PublisherAmerican Chemical Society (ACS)
DOIdoi:10.1021/ja00823a053Search in ResearchGate
Generate Citation Formats
Mindat Ref. ID1326054Long-form Identifiermindat:1:5:1326054:5
GUID0
Full ReferenceStork, Gilbert, Cohen, Jonathan F. (1974) Ring size in epoxynitrile cyclization. General synthesis of functionally substituted cyclobutanes. Application to (+-)-grandisol. Journal Of The American Chemical Society, 96 (16) 5270-5272 doi:10.1021/ja00823a053
Plain TextStork, Gilbert, Cohen, Jonathan F. (1974) Ring size in epoxynitrile cyclization. General synthesis of functionally substituted cyclobutanes. Application to (+-)-grandisol. Journal Of The American Chemical Society, 96 (16) 5270-5272 doi:10.1021/ja00823a053
In(1974, August) Journal Of The American Chemical Society Vol. 96 (16) American Chemical Society (ACS)

See Also

These are possibly similar items as determined by title/reference text matching only.

STORK, GILBERT, COHEN, JONATHAN F. (1974) ChemInform Abstract: RING SIZE IN EPOXYNITRILE CYCLIZATION, A GENERAL SYNTHESIS OF FUNCTIONALLY SUBSTITUTED CYCLOBUTANES, APPLICATION TO (+-)-GRANDISOL. Chemischer Informationsdienst, 5 (42) doi:10.1002/chin.197442217
Stork, Gilbert, Cama, Lovji D., Coulson, D. R. (1974) Epoxynitrile cyclization. General method of ring formation. Journal Of The American Chemical Society, 96 (16) 5268-5270 doi:10.1021/ja00823a052
STORK, GILBERT, CAMA, LOVJI D., COULSON, D. R. (1974) ChemInform Abstract: EPOXYNITRILE CYCLIZATION, A GENERAL METHOD FOR RING FORMATION. Chemischer Informationsdienst, 5 (42) doi:10.1002/chin.197442137
Stork, Gilbert, Maldonado, Luis (1974) Conjugate addition of acyl carbanion equivalents via the protected cyanohydrin method. Journal Of The American Chemical Society, 96 (16) 5272-5274 doi:10.1021/ja00823a054
Stork, Gilbert, Szajewski, Richard P. (1974) Carboxy .beta.-lactams by photochemical ring contraction. Journal Of The American Chemical Society, 96 (18) 5787-5791 doi:10.1021/ja00825a015
Stork, Gilbert, Singh, Janak (1974) Regiospecific Michael reactions in aprotic solvents with .alpha.-silylated electrophilic olefins. Application to annelation reactions. Journal Of The American Chemical Society, 96 (19) 6181-6182 doi:10.1021/ja00826a038
Meyers, A. I., Fleming, Steven A. (1986) Efficient asymmetric (2 + 2) photocycloaddition leading to chiral cyclobutanes. Application to the total synthesis of (-)-grandisol. Journal Of The American Chemical Society, 108 (2) 306-307 doi:10.1021/ja00262a026
Stork, Gilbert, Kahn, Michael (1985) Control of ring junction stereochemistry via radical cyclization. Journal Of The American Chemical Society, 107 (2) 500-501 doi:10.1021/ja00288a038
Stork, Gilbert, Isobe, Minoru (1975) General approach to prostaglandins via methylenecyclopentanones. Total synthesis of (+-)-prostaglandin F2.alpha. Journal Of The American Chemical Society, 97 (16) 4745-4746 doi:10.1021/ja00849a042
Stork, Gilbert, Jung, Michael E., Colvin, Ernest, Noel, Yves (1974) Synthetic routes to halomethyl vinylsilanes. Journal Of The American Chemical Society, 96 (11) 3684-3686 doi:10.1021/ja00818a071
Stork, Gilbert., Darling, S. D., Harrison, Ian T., Wharton, Peter S. (1962) A Stereospecific Total Synthesis of 18-Substituted Steroids. Application to the Synthesis ofdl-Conessine. Journal Of The American Chemical Society, 84 (10) 2018-2020 doi:10.1021/ja00869a060
 
and/or  
Mindat.org is an outreach project of the Hudson Institute of Mineralogy, a 501(c)(3) not-for-profit organization.
Copyright © mindat.org and the Hudson Institute of Mineralogy 1993-2025, except where stated. Most political location boundaries are Β© OpenStreetMap contributors. Mindat.org relies on the contributions of thousands of members and supporters. Founded in 2000 by Jolyon Ralph.
To cite: Ralph, J., Von Bargen, D., Martynov, P., Zhang, J., Que, X., Prabhu, A., Morrison, S. M., Li, W., Chen, W., & Ma, X. (2025). Mindat.org: The open access mineralogy database to accelerate data-intensive geoscience research. American Mineralogist, 110(6), 833–844. doi:10.2138/am-2024-9486.
Privacy Policy - Terms & Conditions - Contact Us / DMCA issues - Report a bug/vulnerability Current server date and time: September 9, 2025 13:06:03
Go to top of page