Abstract
A seven-step route to diols (1) and (2) is described, along with a pathway for achieving incorporation of the aliphatic chain of 2 into a cyclohexane core.
| Original language | English |
|---|---|
| Pages (from-to) | 27-30 |
| Number of pages | 4 |
| Journal | Heterocycles |
| Volume | 50 |
| Issue number | 1 |
| Publication status | Published - 1999 Jan 1 |
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All Science Journal Classification (ASJC) codes
- Analytical Chemistry
- Pharmacology
- Organic Chemistry
Cite this
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Synthesis of meso- and dl-2,2'-methylenebis[tetrahydro-2-furanmethanol]. Potential building blocks for the construction of ionophores housing spirotetrahydrofuranyl motifs. / Paquette, Leo A.; Stearns, Brian A.; Mooney, Pamela A.; Tae, Jinsung.
In: Heterocycles, Vol. 50, No. 1, 01.01.1999, p. 27-30.Research output: Contribution to journal › Article
TY - JOUR
T1 - Synthesis of meso- and dl-2,2'-methylenebis[tetrahydro-2-furanmethanol]. Potential building blocks for the construction of ionophores housing spirotetrahydrofuranyl motifs
AU - Paquette, Leo A.
AU - Stearns, Brian A.
AU - Mooney, Pamela A.
AU - Tae, Jinsung
PY - 1999/1/1
Y1 - 1999/1/1
N2 - A seven-step route to diols (1) and (2) is described, along with a pathway for achieving incorporation of the aliphatic chain of 2 into a cyclohexane core.
AB - A seven-step route to diols (1) and (2) is described, along with a pathway for achieving incorporation of the aliphatic chain of 2 into a cyclohexane core.
UR - http://www.scopus.com/inward/record.url?scp=0032838967&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0032838967&partnerID=8YFLogxK
M3 - Article
VL - 50
SP - 27
EP - 30
JO - Heterocycles
JF - Heterocycles
SN - 0385-5414
IS - 1
ER -