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Tanaka et al.¡¯s Ru(I)-catalyzed [2 + 2 + 2] cyclotrimerization of ethyl cyanoformate (28, 29) also proceeded effectively for diynes 4a,b,d, to afford pyrrolopyridine carboxylates 28a,b,d regioselectively. Deiters and coworkers have carried out similar reactions previously on solid support (27, 30). Similarly, Saito and coworkers¡¯ Ni(0)-catalyzed [3 + 2 + 2] cycloaddition with ethyl cyclopropylidene acetate (31) was translated effectively to solid support-bound diynes 4a¨Cc. The initial cycloheptapyrrolidine ester products were then converted to the correspondingWeinreb amides 29a¨Cc/29¡äa¨Cc (32) to facilitate downstream separation of E and Z isomers after cleavage from the solid support. |
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lgq101(½ð±Ò+15, ·ÒëEPI+1): лл~~~~~ 2011-06-24 12:16:53
Mally89(½ð±Ò+1): ¸ÐлӦÖú£¡~ 2011-06-24 21:36:36
lgq101(½ð±Ò+15, ·ÒëEPI+1): лл~~~~~ 2011-06-24 12:16:53
Mally89(½ð±Ò+1): ¸ÐлӦÖú£¡~ 2011-06-24 21:36:36
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Tanaka et al.¡¯s Ru(I)-catalyzed [2 + 2 + 2] cyclotrimerization of ethyl cyanoformate (28, 29) also proceeded effectively for diynes 4a,b,d, to afford pyrrolopyridine carboxylates 28a,b,d regioselectively. TanakaµÈµÄÇè¼×ËáÒÒõ¥îÉ´ß»¯[2 + 2 + 2]»·Èý¾Û·´Ó¦Ò²¿É¸ßЧµØÒÔ¶þȲ4a¡¢b¡¢dΪµ×Îï½øÐв¢Ìá¹©ÇøÓòÑ¡ÔñÐÔ¡£Deiters and coworkers have carried out similar reactions previously on solid support (27, 30). Deiters¼°ÆäͬÊÂÏÈǰÔÚ¹ÌÏàÔØÌåÉϽøÐÐÁËÏàËÆµÄ·´Ó¦¡£ Similarly, Saito and coworkers¡¯ Ni(0)-catalyzed [3 + 2 + 2] cycloaddition with ethyl cyclopropylidene acetate (31) was translated effectively to solid support-bound diynes 4a¨Cc. ÓëÉÏÊöÀàËÆ£¬Saito¼°ÆäͬʵÄethyl cyclopropylidene acetate Äø´ß»¯[3 + 2 + 2] »·»¯¼Ó³ÉÒ²±»ÓÐЧµØÒýÈëµ½¶þȲ4a-cΪµ×ÎïµÄµÄ¹ÌÏàÔØÌåºÏ³ÉÖС£ The initial cycloheptapyrrolidine ester products were then converted to the corresponding Weinreb amides 29a¨Cc/29¡äa¨Cc (32) to facilitate downstream separation of E and Z isomers after cleavage from the solid support.×î³õµÄcycloheptapyrrolidine ester²úÎïËæºó±»×ª»¯ÎªÏàÓ¦µÄWeinrebõ£°·29a¨Cc/29¡äa¨Cc£¬ÒÔÀûÓÚEºÍZͬ·ÖÒì¹¹Ìå´ÓÔØÌåÉϽâÀëÏÂÀ´ºóµÄÏÂÓηÖÀë¡£ |
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