Asymmetric reductive cyclization using the intramolecular conjugate addition of enolates onto α,β-unsaturated sulfoxides
Tetrahedron letters Volume 39 Issue 1-2
Page 47-50
published_at 1998-01-01
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| File | |
| Title ( eng ) |
Asymmetric reductive cyclization using the intramolecular conjugate addition of enolates onto α,β-unsaturated sulfoxides
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| Creator |
Yoshizaki Hiroki
Tanaka Tadashi
Yoshii Eiichi
Koizumi Toru
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| Source Title |
Tetrahedron letters
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| Volume | 39 |
| Issue | 1-2 |
| Start Page | 47 |
| End Page | 50 |
| Abstract |
Li(sec-Bu)3BH-mediated reductive cyclization of optically pure 8-((S)-p-tolylsulfinyl)-(2E,7Z)-octadienoate 9 and 7-(p-tolylsulfinyl)-2,6-heptadienoate 16 afforded trans-2-((p-tolylsulfinyl)-methyl)cyclohexane-1-carboxylate and trans-2-((p-tolylsulfinyl)methyl)cyclopentane-1-carboxylate, respectively, as a single isomer.
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| NDC |
Chemistry [ 430 ]
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| Language |
eng
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| Resource Type | journal article |
| Publisher |
Elsevier B.V.
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| Date of Issued | 1998-01-01 |
| Rights |
Copyright (c) 1998 Elsevier B.V.
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| Publish Type | Author’s Original |
| Access Rights | open access |
| Source Identifier |
[ISSN] 0040-4039
[DOI] 10.1016/S0040-4039(97)10414-2
[DOI] http://dx.doi.org/10.1016/S0040-4039(97)10414-2
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