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Tetrahedron Letters

Volumn 28, Issue 30, 1987, Pages 3445-3448

DBP ylides: Wittig reagents for synthesis of E-alkenes from aldehydes

(2) Vedejs, E a Marth, C a

a UNIVERSITY OF WISCONSIN MADISON (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0000089380 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4039(00)96322-6 Document Type: Article

Times cited : (37)

References (25)

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8
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10
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- Dibenzophospholium salts and ylides. Preparation, properties, and Wittig olefin synthesis
- 3P analogs
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11
- 84918462193
- 2) into a thick walled tube suitable for sealing. The liquid was cooled (−78°) under vacuum, the tube was sealed, and then heated 30 min at 110 °C to decompose the oxaphosphetanes. [[Truncated]]

12
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- 7b

13
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- Maryanoff¹ Reitz² Mutter³ Inners⁴ Almond⁵ Whittle⁶ Olofson⁷

14
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- Vedejs, E.; Marth, C. M.; Ruggeri, R., unpublished results.

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16
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17
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18
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- 31P NMR: 3c, −64.1 ppm; 4c, −65.5 ppm, −23 °C, THF.

19
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- 31P NMR resolution of oxaphosphetane diastereomers
- (1986) J. Am. Chem. Soc. , vol.108 , pp. 7664
- Maryanoff¹ Reitz² Mutter³ Inners⁴ Almond⁵ Whittle⁶ Olofson⁷

20
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- for NMR characterization of oxaphosphetanes, see
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21
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- Perkin Trans. I
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24
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- threo-3-Hydroxycarboxylic acids as key intermediates in a highly stereoselective synthesis of (Z)- and (E)-olefins and enol ethers
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- Mulzer¹ Pointner² Chucholowski³ Bruntrup⁴

25
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- Trans-Selective Olefin Syntheses
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.