A HIGHLY STEREOSELECTIVE SYNTHESIS OF RACEMIC JUVENILE HORMONE

[1] ALLYLIC HALOGENATION OF METHYL 3-METHYLBUT-2-ENOATE [J]. JOURNAL OF THE CHEMICAL SOCIETY C-ORGANIC, 1968, (02): : 185 - +

[2] A HIGHLY STEREOSELECTIVE SYNTHESIS OF TRANS-TRISUBSTITUTED OLEFINIC BONDS [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1968, 90 (11) : 2882 - +

[3] THE PREPARATION OF METHYL ESTERS [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1948, 70 (09) : 3135 - 3136

[4] A USEFUL METHOD FOR CONVERSION OF ALCOHOLS INTO IODIDES [J]. JOURNAL OF ORGANIC CHEMISTRY, 1967, 32 (12) : 4160 - &

[5] CORNFORTH JW, 1869, J CHEM SOC, P2539

[6] JUVENILE HORMONE .V. SYNTHESIS OF RACEMIC JUVENILE HORMONE [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1967, 89 (20) : 5292 - &

[7] DAHM KH, 1968, LIFE SCI PT 1 PHYSI, V7, P129

[8] JULIA M, 1960, B SOC CHIM FR, P1381

[9] Kosower E. M., 1963, J ORG CHEM, V28, P630, DOI DOI 10.1021/JO01038A007

[10] A HIGHLY PURIFIED PREPARATION OF JUVENILE HORMONE FROM SILK MOTH HYALOPHORA CECROPIA L [J]. NATURE, 1965, 206 (4981) : 272 - +

[1] ALLYLIC HALOGENATION OF METHYL 3-METHYLBUT-2-ENOATE [J]. JOURNAL OF THE CHEMICAL SOCIETY C-ORGANIC, 1968, (02): : 185 - +

[2] A HIGHLY STEREOSELECTIVE SYNTHESIS OF TRANS-TRISUBSTITUTED OLEFINIC BONDS [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1968, 90 (11) : 2882 - +

[3] THE PREPARATION OF METHYL ESTERS [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1948, 70 (09) : 3135 - 3136

[4] A USEFUL METHOD FOR CONVERSION OF ALCOHOLS INTO IODIDES [J]. JOURNAL OF ORGANIC CHEMISTRY, 1967, 32 (12) : 4160 - &

[5] CORNFORTH JW, 1869, J CHEM SOC, P2539

[6] JUVENILE HORMONE .V. SYNTHESIS OF RACEMIC JUVENILE HORMONE [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1967, 89 (20) : 5292 - &

[7] DAHM KH, 1968, LIFE SCI PT 1 PHYSI, V7, P129

[8] JULIA M, 1960, B SOC CHIM FR, P1381

[9] Kosower E. M., 1963, J ORG CHEM, V28, P630, DOI DOI 10.1021/JO01038A007

[10] A HIGHLY PURIFIED PREPARATION OF JUVENILE HORMONE FROM SILK MOTH HYALOPHORA CECROPIA L [J]. NATURE, 1965, 206 (4981) : 272 - +