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Protection, blocking, masking esters

Carreira and co-workers have also extended the scope of aldehydes that may be utilized in catalytic addition reactions to include stannylpropenal 108 as a substrate (Table 8B2.12, Entry 7). The adduct produced from the aldol addition of 105 is isolated with 92% ee and serves as a useful building block, as it is amenable for further synthetic elaboration (Scheme 8B2.9). Thus, vinylstannane 109 is a substrate for Stille cross-coupling reactions to give a diverse family of protected acetoacetate adducts 110. Following deprotection of the masked keto ester, the corresponding hydroxy keto ester 111 may be converted to either the syn or anti skipped polyols 112 or 113. A recent total synthesis of macrolactin A by Carreira and co-workers utilizes aldol... [Pg.534]


See other pages where Protection, blocking, masking esters is mentioned: [Pg.103]    [Pg.546]    [Pg.547]    [Pg.575]    [Pg.264]    [Pg.239]    [Pg.917]    [Pg.919]    [Pg.197]    [Pg.199]    [Pg.56]    [Pg.24]    [Pg.148]    [Pg.169]    [Pg.137]    [Pg.83]    [Pg.39]    [Pg.270]    [Pg.244]    [Pg.155]    [Pg.329]   
See also in sourсe #XX -- [ Pg.21 , Pg.140 ]

See also in sourсe #XX -- [ Pg.17 , Pg.20 , Pg.172 , Pg.271 ]

See also in sourсe #XX -- [ Pg.17 , Pg.271 ]

See also in sourсe #XX -- [ Pg.17 , Pg.271 ]

See also in sourсe #XX -- [ Pg.15 , Pg.27 ]




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