(\pm)-Chrysolic acid $[I; R = CH_2CH_2C(OH)MeCH_2CO_2R_1, R_1 = H]$ was prepd. in 4 steps from I (R = H). MeCOCH_2CO_2Et was alkylated with I (R = CH2Cl), followed by deethoxycarbonylation to give I (R = CH_2CH_2COMe). Reformatsky reaction of I with $BrCH_2CO_2R_1 (R_1 = CMe_3, Me)$ gave $I [R = CH_2CH_2C(OH)MeCH_2CO_2R_1, R_1 = H, Me, resp.]$ after work up
Section A. Synthesis of (+)-trans-Chrysanthemic Acid and some Analogues. (+)-trans-Chrysanthemic aci...
Starting from Me 4-phenylbutanoate, p-R1C6H4CH2CH2CH2R (I; R = CO2Me, R1 = H), the synthesis of 1,1-...
Starting from Me 4-phenylbutanoate, p-R1C6H4CH2CH2CH2R (I; R = CO2Me, R1 = H), the synthesis of 1,1-...
Sydonic acid $[I; R = C(OH)Me CH_2CH_2CH_2CHMe_2, R_1 = R_3 = H, R_2 = CO_2H]$ was prepd. in 2 steps...
Sydonic acid $[I; R = C(OH)Me CH_2CH_2CH_2CHMe_2, R_1 = R_3 = H, R_2 = CO_2H]$ was prepd. in 2 steps...
Chloride I $(R=Cl, R_1=CMe_3)$, obtained from $2,4-Me_2C_6H_3OH$, was converted into the cyanomethyl...
Chloride I $(R=Cl, R_1=CMe_3)$, obtained from $2,4-Me_2C_6H_3OH$, was converted into the cyanomethyl...
Monoterpenic hydroquinone di-Me ethers I (R = Me, CHO) were synthesized starting from a common inter...
Section A. Synthesis of (+)-trans-Chrysanthemic Acid and some Analogues. (+)-trans-Chrysanthemic aci...
$p-RC_6H_4CHMeCH_2COCH_2CHMe_2$ (I; R=CHO) was prepared from chiral I CR=Me) by oxidation to I $(R=C...
$p-RC_6H_4CHMeCH_2COCH_2CHMe_2$ (I; R=CHO) was prepared from chiral I CR=Me) by oxidation to I $(R=C...
Department of Chemistry, Panjab University, Chandigarh-160014. Manuscript received 26 August 1974 ;...
Department of Chemistry, Panjab University, Chandigarh Manuscript received 28 September 1974; revis...
This study involved the preparation of mycolic acid (ll) containing a double bond in a cis configura...
Mycophenolic acid (28) has been obtained by a convergent synthesis starting from methyl 6-bromo-4-me...
Section A. Synthesis of (+)-trans-Chrysanthemic Acid and some Analogues. (+)-trans-Chrysanthemic aci...
Starting from Me 4-phenylbutanoate, p-R1C6H4CH2CH2CH2R (I; R = CO2Me, R1 = H), the synthesis of 1,1-...
Starting from Me 4-phenylbutanoate, p-R1C6H4CH2CH2CH2R (I; R = CO2Me, R1 = H), the synthesis of 1,1-...
Sydonic acid $[I; R = C(OH)Me CH_2CH_2CH_2CHMe_2, R_1 = R_3 = H, R_2 = CO_2H]$ was prepd. in 2 steps...
Sydonic acid $[I; R = C(OH)Me CH_2CH_2CH_2CHMe_2, R_1 = R_3 = H, R_2 = CO_2H]$ was prepd. in 2 steps...
Chloride I $(R=Cl, R_1=CMe_3)$, obtained from $2,4-Me_2C_6H_3OH$, was converted into the cyanomethyl...
Chloride I $(R=Cl, R_1=CMe_3)$, obtained from $2,4-Me_2C_6H_3OH$, was converted into the cyanomethyl...
Monoterpenic hydroquinone di-Me ethers I (R = Me, CHO) were synthesized starting from a common inter...
Section A. Synthesis of (+)-trans-Chrysanthemic Acid and some Analogues. (+)-trans-Chrysanthemic aci...
$p-RC_6H_4CHMeCH_2COCH_2CHMe_2$ (I; R=CHO) was prepared from chiral I CR=Me) by oxidation to I $(R=C...
$p-RC_6H_4CHMeCH_2COCH_2CHMe_2$ (I; R=CHO) was prepared from chiral I CR=Me) by oxidation to I $(R=C...
Department of Chemistry, Panjab University, Chandigarh-160014. Manuscript received 26 August 1974 ;...
Department of Chemistry, Panjab University, Chandigarh Manuscript received 28 September 1974; revis...
This study involved the preparation of mycolic acid (ll) containing a double bond in a cis configura...
Mycophenolic acid (28) has been obtained by a convergent synthesis starting from methyl 6-bromo-4-me...
Section A. Synthesis of (+)-trans-Chrysanthemic Acid and some Analogues. (+)-trans-Chrysanthemic aci...
Starting from Me 4-phenylbutanoate, p-R1C6H4CH2CH2CH2R (I; R = CO2Me, R1 = H), the synthesis of 1,1-...
Starting from Me 4-phenylbutanoate, p-R1C6H4CH2CH2CH2R (I; R = CO2Me, R1 = H), the synthesis of 1,1-...