Vote for your favorite mineral in #MinCup25! - Taenite vs. Nontronite
It's a mineral found mostly in the farthest reaches of space vs one so common an exhaustive list of localities is nigh impossible as alloy #taenite faces off against clay #nontronite.
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

Sumida, Shin-ichi, Ohga, Masanori, Mitani, Junji, Nokami, Junzo (2000) New and Stereoselective Synthesis of 1,4-Disubstituted Buten-4-ols (Homoallylic Alcohol α-Adducts) from the Corresponding γ-Isomers (3,4-Disubstituted Buten-4-ols) via an Acid-Catalyzed Allyl-Transfer Reaction with Aldehydes. Journal Of The American Chemical Society, 122 (7) 1310-1313 doi:10.1021/ja990057p

Advanced
   -   Only viewable:
Reference TypeJournal (article/letter/editorial)
TitleNew and Stereoselective Synthesis of 1,4-Disubstituted Buten-4-ols (Homoallylic Alcohol α-Adducts) from the Corresponding γ-Isomers (3,4-Disubstituted Buten-4-ols) via an Acid-Catalyzed Allyl-Transfer Reaction with Aldehydes
JournalJournal Of The American Chemical Society
AuthorsSumida, Shin-ichiAuthor
Ohga, MasanoriAuthor
Mitani, JunjiAuthor
Nokami, JunzoAuthor
Year2000 (February)Volume122
Issue7
PublisherAmerican Chemical Society (ACS)
DOIdoi:10.1021/ja990057pSearch in ResearchGate
Generate Citation Formats
Mindat Ref. ID1569785Long-form Identifiermindat:1:5:1569785:9
GUID0
Full ReferenceSumida, Shin-ichi, Ohga, Masanori, Mitani, Junji, Nokami, Junzo (2000) New and Stereoselective Synthesis of 1,4-Disubstituted Buten-4-ols (Homoallylic Alcohol α-Adducts) from the Corresponding γ-Isomers (3,4-Disubstituted Buten-4-ols) via an Acid-Catalyzed Allyl-Transfer Reaction with Aldehydes. Journal Of The American Chemical Society, 122 (7) 1310-1313 doi:10.1021/ja990057p
Plain TextSumida, Shin-ichi, Ohga, Masanori, Mitani, Junji, Nokami, Junzo (2000) New and Stereoselective Synthesis of 1,4-Disubstituted Buten-4-ols (Homoallylic Alcohol α-Adducts) from the Corresponding γ-Isomers (3,4-Disubstituted Buten-4-ols) via an Acid-Catalyzed Allyl-Transfer Reaction with Aldehydes. Journal Of The American Chemical Society, 122 (7) 1310-1313 doi:10.1021/ja990057p
In(2000, February) Journal Of The American Chemical Society Vol. 122 (7) American Chemical Society (ACS)

See Also

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

Nokami, Junzo, Anthony, Laurence, Sumida, Shin-ichi (2000) New Route toα-Adducts of Homoallylic Alcohols by an Acid-Catalyzed Stereospecific Allyl-Transfer Reaction fromγ-Adducts. Chemistry - A European Journal, 6 (16). 2909-2913 doi:10.1002/1521-3765(20000818)6:16<2909::aid-chem2909>3.0.co;2-2
Nokami, Junzo, Yoshizane, Kenji, Matsuura, Hiroyuki, Sumida, Shin-ichi (1998) New Concept in the Allylation of Aldehydes:  Regiospecific Allylation of Aldehydes by an Allyl-Transfer Reaction of Homoallylic Alcohols. Journal Of The American Chemical Society, 120 (26) 6609-6610 doi:10.1021/ja9810742
Nokami, Junzo, Ohga, Masanori, Nakamoto, Hitoshi, Matsubara, Tadahiro, Hussain, Iqbal, Kataoka, Kazuhide (2001) The First and Highly Enantioselective Crotylation of Aldehydes via an Allyl-Transfer Reaction from a Chiral Crotyl-Donor. Journal Of The American Chemical Society, 123 (37) 9168-9169 doi:10.1021/ja011257f
Shafi, Siddiqi M., Chou, Jingyu, Kataoka, Kazuhide, Nokami, Junzo (2005) Stereoselective 4-Benzyloxybut-2-enylation of Aldehydes via an Allyl-Transfer Reaction Using a Chiral Allyl Donor. Organic Letters, 7. 2957-2960 doi:10.1021/ol050890t
Brown, Herbert Charles, Suzuki, Akira, Miyaura, Norio, Itoh, Mitsuomi, Holland, George W., Negishi, Eichi (1971) New four-carbon-atom homologation involving the free-radical chain reaction of 1,3-butadiene monoxide with organoboranes. Synthesis of 4-alkyl-2-buten-1-ols from olefins via hydroboration. Journal Of The American Chemical Society, 93 (11) 2792-2793 doi:10.1021/ja00740a040
Hayashi, Sayuri, Hirano, Koji, Yorimitsu, Hideki, Oshima, Koichiro (2005) Gallium-Mediated Allyl Transfer from Bulky Homoallylic Alcohol to Aldehydes via Retro-allylation:  Stereoselective Synthesis of Botherythro- andthreo-Homoallylic Alcohols1. Organic Letters, 7. 3577-3579 doi:10.1021/ol0515199
Nokami, Junzo, Nomiyama, Kenta, Shafi, Siddiqi M., Kataoka, Kazuhide (2004) A Novel Enantioselective (2Z)-Alk-2-enylation of Aldehydes via an Allyl-Transfer Reaction from Chiral Allyl Donors Prepared from (+)-Isomenthone. Organic Letters, 6. 1261-1264 doi:10.1021/ol0400140
MOELLER, R., ENGEL, N., STEGLICH, W. (1978) ChemInform Abstract: PREPARATION OF (E)-3-ALKOXY- AND (E)-3-(ALKYLTHIO)BUTEN-2-OLS AND THE CORRESPONDING ALDEHYDES. Chemischer Informationsdienst, 9 (50) doi:10.1002/chin.197850140
Wenglowsky, Steve, Hegedus, Louis S. (1998) An Asymmetric Synthesis of Optically Pure α,α-Disubstituted Amino Aldehydes, α,α-Disubstituted Amino Acids, and Sterically Demanding Dipeptides. Journal Of The American Chemical Society, 120 (48) 12468-12473 doi:10.1021/ja9823518
Ma, Shengming, Zhao, Shimin (2001) Novel Substituent and Chelating Effects in the Pd-Catalyzed Reaction of 2,3-Allenols, Aryl Iodides, and Amines. Highly Regio- and Stereoselective Synthesis of 2-Amino-3-alken-1-ols or 4-Amino-2(E)-alken-1-ols. Journal Of The American Chemical Society, 123 (23) 5578-5579 doi:10.1021/ja0035553
Miura, Katsukiyo, Okajima, Shigeo, Hondo, Takeshi, Nakagawa, Takahiro, Takahashi, Tatsuyuki, Hosomi, Akira (2000) Acid-Catalyzed Cyclization of Vinylsilanes Bearing a Hydroxy Group:  A New Method for Stereoselective Synthesis of Disubstituted Tetrahydrofurans1. Journal Of The American Chemical Society, 122 (46) 11348-11357 doi:10.1021/ja002496q
 
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 © 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 15, 2025 07:14:35
Go to top of page