✦ LIBER ✦

Enantiospecific synthesis of (R)-1,6-dioxaspiro[4.5]decane from a derivative of d-fructose

✍ Scribed by Isidoro Izquierdo Cubero; Maria T. Plaza López-Espinosa; Anthony C. Richardson; Kai H. Aamlid

Book ID: 107727216
Publisher: Elsevier Science
Year: 1993
Tongue: English
Weight: 412 KB
Volume: 242
Category: Article
ISSN: 0008-6215
DOI: 10.1016/0008-6215(93)80042-d

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Enantiospecific synthesis fromd-fructose

Enantiospecific synthesis fromd-fructose of (2S,5R)- and (2R,5R)-2-methyl-1,6-dioxaspiro[4.5]decane [the odor bouquet minor components ofParavespula vulgaris(L.)]

✍ Isidoro Izquierdo Cubero; Maria T. Plaza Lopez-Espinosa; Anthony C. Richardson 📂 Article 📅 1993 🏛 Springer 🌐 English ⚖ 1014 KB

Enantiospecific synthesis of (R)-1,7-dio

Enantiospecific synthesis of (R)-1,7-dioxaspiro [5.5]undecane [major component of olive fruit fly (Dacus Oleae) sex pheromone] from d-Fructose

✍ Isidoro Izquierdo Cubero; Maria T. Plaza López-Espinosa; Rafael Acuña Castillo 📂 Article 📅 1991 🏛 Springer 🌐 English ⚖ 581 KB

Synthesis and conformation of 6,8,10-tri

Synthesis and conformation of 6,8,10-trinitro-1,4-dioxaspiro[4.5]decane

✍ Yu. M. Atroshchenko; S. S. Golotvin; I. V. Shakhkel'dyan; O. V. Shishkin; Zh. O. 📂 Article 📅 1999 🏛 Springer 🌐 English ⚖ 391 KB

Alkyl-1,6-dioxaspiro[4.5]-decanes — A ne

Alkyl-1,6-dioxaspiro[4.5]-decanes — A new class of pheromones

✍ W. Francke; G. Hindorf; W. Reith 📂 Article 📅 1979 🏛 Springer 🌐 English ⚖ 204 KB

Spiroketal equilibration: Interconversio

Spiroketal equilibration: Interconversion of 1,6-dioxaspiro[4.4]nonanes and 1,6-dioxaspiro[4.5]decanes. Implications for the synthesis of cephalostatin 7

✍ Jae Uk Jeong; P.L. Fuchs 📂 Article 📅 1994 🏛 Elsevier Science 🌐 French ⚖ 279 KB

Acid-catalyzed equilibration of spiroketals 5SHp6 and 55Haj3 involves a two stage process whereby the 1,6-dioxaspiro]4.4]nonanes can be equilibrated under mild conditions to a pair of 1,6\_dioxaspiro[45]decanes with preservation of the adjacent C-20 methyl stereocenter. Under more forcing conditions

Synthesis of methyl-1,6-dioxaspiro[4,5]d

Synthesis of methyl-1,6-dioxaspiro[4,5]decanes using organoselenium mediated cyclization reactions

✍ Steven V. Ley; Barry Lygo 📂 Article 📅 1982 🏛 Elsevier Science 🌐 French ⚖ 176 KB

Three naturally occurring methyl-1,6-dioxaspiro[4.5]decanes have been prepared in good yield using organoselenium mediated reactions during the crucial cyclization process.