ChemInform Abstract: CARBENE REARRANGEMENT. PART 18. SPIROACETAL FORMATION BY CARBENE(CARBENOID) INSERTION REACTION: SYNTHESIS OF THE MAIN COMPONENTS OF THE SEX ATTRACTANT OF THE OLIVE FLY (DACUS OLEAE)

U. H. BRINKER; A. HAGHANI; K. GOMANN

doi:10.1002/chin.198528363

ChemInform Abstract: CARBENE REARRANGEMENT. PART 18. SPIROACETAL FORMATION BY CARBENE(CARBENOID) INSERTION REACTION: SYNTHESIS OF THE MAIN COMPONENTS OF THE SEX ATTRACTANT OF THE OLIVE FLY (DACUS OLEAE)

Chemischer Informationsdienst ◽

10.1002/chin.198528363 ◽

1985 ◽

Vol 16 (28) ◽

Author(s):

U. H. BRINKER ◽

A. HAGHANI ◽

K. GOMANN

Keyword(s):

Sex Attractant ◽

Insertion Reaction ◽

Reaction Synthesis ◽

Dacus Oleae ◽

Olive Fly ◽

Main Components

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Spiroacetal Formation by Carbene (Carbenoid) Insertion Reaction: Synthesis of the Major Constituent of the Sex Attractant of the Olive Fly (Dacus oleae)

Angewandte Chemie International Edition in English ◽

10.1002/anie.198502301 ◽

1985 ◽

Vol 24 (3) ◽

pp. 230-231 ◽

Cited By ~ 8

Author(s):

Udo H. Brinker ◽

Ali Haghani ◽

Klaus Gomann

Keyword(s):

Sex Attractant ◽

Major Constituent ◽

Insertion Reaction ◽

Reaction Synthesis ◽

Dacus Oleae ◽

Olive Fly

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ChemInform Abstract: Aminopalladation-Triggered Carbene Insertion Reaction: Synthesis of 2-(1H-Indol-3-yl)acetates.

ChemInform ◽

10.1002/chin.201530165 ◽

2015 ◽

Vol 46 (30) ◽

pp. no-no

Author(s):

Ziwei Hu ◽

Shuang Luo ◽

Qiang Zhu

Keyword(s):

Insertion Reaction ◽

Reaction Synthesis ◽

Carbene Insertion

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Application of the double intramolecular hetero-Michael addition (DIHMA) approach in spiroketal synthesis: total synthesis of (±)-(4S,6S)-4-hydroxy-1,7-dioxaspiro[5.5]undecane, a Dacus oleae olive fly pheromone

Tetrahedron Letters ◽

10.1016/s0040-4039(01)02084-6 ◽

2002 ◽

Vol 43 (1) ◽

pp. 1-2 ◽

Cited By ~ 16

Author(s):

Junliang Hao ◽

Craig J Forsyth

Keyword(s):

Total Synthesis ◽

Michael Addition ◽

Dacus Oleae ◽

Olive Fly

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THE OLIVE FLY (DACUS OLEAE GMEL.) IN CRETE, GREECE

Acta Horticulturae ◽

10.17660/actahortic.1990.286.76 ◽

1990 ◽

pp. 371-374 ◽

Cited By ~ 6

Author(s):

S.E. Michelakis

Keyword(s):

Dacus Oleae ◽

Olive Fly

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Isolation and synthesis of 3- and 4-hydroxy-1,7-dioxaspiro[5.5]undecanes from the olive fly (Dacus oleae)

Journal of the Chemical Society Chemical Communications ◽

10.1039/c39820000601 ◽

1982 ◽

pp. 601 ◽

Cited By ~ 35

Author(s):

Raymond Baker ◽

Richard H. Herbert ◽

Andrew H. Parton

Keyword(s):

Dacus Oleae ◽

Olive Fly

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A facile synthesis of (−)- and (+)-Geissman–Waiss lactone via intramolecular Rh(II)-carbenoid mediated C–H insertion reaction: synthesis of (1R,7R,8R)-turneforcidine

Tetrahedron Letters ◽

10.1016/s0040-4039(00)01664-6 ◽

2000 ◽

Vol 41 (47) ◽

pp. 9025-9029 ◽

Cited By ~ 16

Author(s):

Andrew G.H Wee

Keyword(s):

Insertion Reaction ◽

Reaction Synthesis ◽

Facile Synthesis

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Identification and synthesis of the major sex pheromone of the olive fly (Dacus oleae)

Journal of the Chemical Society Chemical Communications ◽

10.1039/c39800000052 ◽

1980 ◽

pp. 52 ◽

Cited By ~ 92

Author(s):

Raymond Baker ◽

Richard Herbert ◽

Philip E. Howse ◽

Owen T. Jones ◽

Wittko Francke ◽

...

Keyword(s):

Sex Pheromone ◽

Dacus Oleae ◽

Olive Fly

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Note on the Control of Olive Fly (Dacus oleae [Gmel.]) by Means of Low and Ultra-low Volume Bait-spraying

EPPO Bulletin ◽

10.1111/j.1365-2338.1971.tb02552.x ◽

1971 ◽

Vol 1 (2) ◽

pp. 63-65

Author(s):

P.S. Orphanidis ◽

P.A. Mourikis ◽

M.C. Souliotis

Keyword(s):

Dacus Oleae ◽

Olive Fly ◽

Low Volume

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Synthesis of Enantiomerically Pure 1,7-Dioxaspiro[5.5]undecanes, Pheromone Components of the Olive Fly (Dacus oleae)

Angewandte Chemie International Edition in English ◽

10.1002/anie.198405191 ◽

1984 ◽

Vol 23 (7) ◽

pp. 519-520 ◽

Cited By ~ 16

Author(s):

Hartmut Redlich ◽

Wittko Francke

Keyword(s):

Dacus Oleae ◽

Enantiomerically Pure ◽

Olive Fly ◽

Pheromone Components

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A SEX ATTRACTANT OF THE OLIVE FRUIT FLY, DACUS OLEAE AND ITS BIOLOGICAL ACTIVITY UNDER LABORATORY AND FIELD CONDITIONS

Entomologia Experimentalis et Applicata ◽

10.1111/j.1570-7458.1977.tb02660.x ◽

1977 ◽

Vol 21 (1) ◽

pp. 81-87 ◽

Cited By ~ 24

Author(s):

G. E. HANIOTAKIS ◽

B. E. MAZOMENOS ◽

J. H. TUMLINSON

Keyword(s):

Biological Activity ◽

Sex Attractant ◽

Fruit Fly ◽

Field Conditions ◽

Olive Fruit Fly ◽

Dacus Oleae ◽

Olive Fruit

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ChemInform Abstract: CARBENE REARRANGEMENT. PART 18. SPIROACETAL FORMATION BY CARBENE(CARBENOID) INSERTION REACTION: SYNTHESIS OF THE MAIN COMPONENTS OF THE SEX ATTRACTANT OF THE OLIVE FLY (DACUS OLEAE)

Spiroacetal Formation by Carbene (Carbenoid) Insertion Reaction: Synthesis of the Major Constituent of the Sex Attractant of the Olive Fly (Dacus oleae)

ChemInform Abstract: Aminopalladation-Triggered Carbene Insertion Reaction: Synthesis of 2-(1H-Indol-3-yl)acetates.

Application of the double intramolecular hetero-Michael addition (DIHMA) approach in spiroketal synthesis: total synthesis of (±)-(4S*,6S*)-4-hydroxy-1,7-dioxaspiro[5.5]undecane, a Dacus oleae olive fly pheromone

THE OLIVE FLY (DACUS OLEAE GMEL.) IN CRETE, GREECE

Isolation and synthesis of 3- and 4-hydroxy-1,7-dioxaspiro[5.5]undecanes from the olive fly (Dacus oleae)

A facile synthesis of (−)- and (+)-Geissman–Waiss lactone via intramolecular Rh(II)-carbenoid mediated C–H insertion reaction: synthesis of (1R,7R,8R)-turneforcidine

Identification and synthesis of the major sex pheromone of the olive fly (Dacus oleae)

Note on the Control of Olive Fly (Dacus oleae [Gmel.]) by Means of Low and Ultra-low Volume Bait-spraying

Synthesis of Enantiomerically Pure 1,7-Dioxaspiro[5.5]undecanes, Pheromone Components of the Olive Fly (Dacus oleae)

A SEX ATTRACTANT OF THE OLIVE FRUIT FLY, DACUS OLEAE AND ITS BIOLOGICAL ACTIVITY UNDER LABORATORY AND FIELD CONDITIONS

Application of the double intramolecular hetero-Michael addition (DIHMA) approach in spiroketal synthesis: total synthesis of (±)-(4S,6S)-4-hydroxy-1,7-dioxaspiro[5.5]undecane, a Dacus oleae olive fly pheromone