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Tetrahedron Letters

Volumn 18, Issue 29, 1977, Pages 2543-2546

Synthesis of γ-methylene butyrolactones (4-penten-4-olides)

(2) Jager V a Gunther H J a

a JUSTUS LIEBIG UNIVERSITY (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0001273218 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4039(01)83815-6 Document Type: Article

Times cited : (61)

References (33)

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11
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14
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17
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18
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19
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- 5a is not necessary nor advisable in the cases described here: a, the allylic alcohols used are easily available, cheap material; b) orthoacetate and the products formed have similar m.w.; distillative as well as hydrolytic work-up is complicated with a large excess of ortho-acetate present.

20
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21
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22
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23
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- 7c.

24
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- 13C NMR spectra.

25
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- 1c,11; the other 4-penten-4-olides 1b, 1c, and 7 are, to the best of our knowledge, new compounds.

26
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- Prepared from dehydronorcampher in three steps (last step thermolytic retro-Diels-Alder reaction); overall yield 43%.

27
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28
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29
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- Lactone aus Allylmalonsäure, Diallylmalonsäure und Diallylessigsäure
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30
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31
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32
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33
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.