Online citations, reference lists, and bibliographies.
Please confirm you are human
(Sign Up for free to never see this)
← Back to Search
DOI: 10.1039/C39800000683

Synthesis Of (±)-lavandulol And Its Related Homoallylic Alcohol Via Allyl Transfer From Sulphur To Tin

Y. Ueno, S. Aoki, M. Okawara
Published 1980 · Chemistry

Save to my Library
Download PDF
Analyze on Scholarcy
Share
(±)-Lavandulol and related homoallylic alcohols were prepared by the stannolysis of allylic sulphones and the subsequent hydroxymethylation of the resulting allylic stannanes with trioxan–BF3·OEt2.



This paper is referenced by
10.1016/B978-0-08-097742-3.00202-0
2.02 Allylsilanes, Allylstannanes, and Related Compounds
P. Ramachandran (2014)
10.1016/J.CES.2004.08.035
A one-step production of fine chemicals using supercritical water: an environmental benign application to the synthesis of monoterpene alcohol
Y. Ikushima (2004)
10.1002/9780470129708.CH3
The Synthesis of Monoterpenes 1980—1986
A. Thomas (2007)
10.1016/B978-0-08-052349-1.00041-X
Allylsilanes, Allylstannanes and Related Systems
I. Fleming (1991)
10.1016/B978-0-408-01435-9.50008-0
Chapter 2 – Preparation of organotin reagents
M. Pereyre (1987)
10.1070/RC2000V069N05ABEH000561
Sulfones and sulfoxides in the total synthesis of biologically active natural compounds
E. N. Prilezhaeva (2000)
Lavandulol – biological activity and synthesis
K. Ciołak (2014)
10.1002/chem.201704099
Photocatalytic Transfer Hydrogenolysis of Allylic Alcohols on Pd/TiO2 : A Shortcut to (S)-(+)-Lavandulol.
Y. Takada (2017)
10.1016/S0040-4020(99)00600-6
Desulfonylation reactions: Recent developments
C. Nájera (1999)
10.1016/S0040-4020(01)80694-3
Stereocontrol in radical cyclizations on sugar templates
Catherine Lesueur (1994)
10.1002/CHIN.198143296
SYNTHESIS OF (.+‐.)‐LAVANDULOL BY THE PRINS REACTION
R. Cookson (1981)
10.1016/B978-0-408-01435-9.50016-X
Chapter 10 – Access to carbon–carbon bonds
M. Pereyre (1987)
10.1016/J.TETLET.2010.01.120
Methyl 3-bromomethyl-3-butenoate as an isopentane building block for the stereoselective preparation of (S)-4-methyl-3,6-dihydro-2H-pyran-2-carbaldehyde and (+)-faranal
I. V. Mineyeva (2010)
10.1002/CHIN.198049136
SYNTHETIC REACTIONS USING ORGANOTIN AND SULFUR COMPOUNDS. 5. SYNTHESIS OF (.+-.)-LAVANDULOL AND ITS RELATED HOMOALLYLIC ALCOHOL VIA ALLYL TRANSFER FROM SULFUR TO TIN
Y. Ueno (1980)
10.1002/EJOC.201300520
A Synthesis of (–)‐(R)‐ and (+)‐(S)‐Lavandulol, (+)‐Lavandulyl 2‐Methylbutanoate, and (+)‐Lavandulyl Senecioate through Ortho­ester Johnson–Claisen Rearrangement
R. A. Fernandes (2013)
10.1021/ol200779y
Selective deoxygenation of allylic alcohol: stereocontrolled synthesis of lavandulol.
H. Kim (2011)
10.1016/B978-0-08-097742-3.00830-2
8.28 Reduction of Sulfur Carbon Bonds and of Other Heteroatoms Bonded to Tetrahedral Carbon
J. M. Manthorpe (2014)
10.1016/B978-0-08-052349-1.00248-1
Reduction of Sulfur–Carbon Bonds and of Other Heteroatoms Bonded to Tetrahedral Carbon
P. Caubère (1991)
Semantic Scholar Logo Some data provided by SemanticScholar