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. Author manuscript; available in PMC: 2008 Sep 14.
Published in final edited form as: J Am Chem Soc. 2005 Jun 22;127(24):8602–8603. doi: 10.1021/ja051526s

Table 1.

Reactions of Various Aldehydes

entry RCHO method temp/time (h) yielda (%) Eeb (%) Product
1 graphic file with name nihms63656t1.jpg A −35/48 53 92 graphic file with name nihms63656t2.jpg
B −25/21 56 91
2 graphic file with name nihms63656t3.jpg A −30/48 57 77 graphic file with name nihms63656t4.jpg
B −15/7 74 86
3 graphic file with name nihms63656t5.jpg A −30/48 64 83 graphic file with name nihms63656t6.jpg
B −15/22 46 87
4 graphic file with name nihms63656t7.jpg A −15/8 52 93 graphic file with name nihms63656t8.jpg
B −15/14 66 92
5 graphic file with name nihms63656t9.jpg A −35/36 51 90 graphic file with name nihms63656t10.jpg
B −20/10 56 91
6 graphic file with name nihms63656t11.jpg A −35/36 47 83 graphic file with name nihms63656t12.jpg
B −20/10 37 85
7a graphic file with name nihms63656t13.jpg B −15/17 59 >99
de
graphic file with name nihms63656t14.jpg
7b graphic file with name nihms63656t15.jpg B −15/18 33 71
de
graphic file with name nihms63656t16.jpg
8 graphic file with name nihms63656t17.jpg B −15/15 33 44 graphic file with name nihms63656t18.jpg
9 graphic file with name nihms63656t19.jpg B −15/14 50 91 graphic file with name nihms63656t20.jpg
10 graphic file with name nihms63656t21.jpg A −35/36 49 98 graphic file with name nihms63656t22.jpg
a

All yields are for isolated pure product.

b

The ee’s were determined by chiral hplc.