In:
Advanced Synthesis & Catalysis, Wiley, Vol. 347, No. 11-13 ( 2005-10), p. 1653-1658
Abstract:
Several kinds of modified guanidines were applied to the trimethylsilylcyanation of 3‐phenylpropanal, cylohexanecarboxaldehyde, pivalaldehyde, and 4‐phenyl‐2‐butanone. Good to moderate enantioselectivity was obtained, even on a ketonic substrate, when a C 2 ‐symmetrical bicyclic guanidine, (2 S ,3 S ,7 S ,8 S )‐tetraphenyl‐1,4,8‐triaza[2.2.0]bicyclooct‐4‐ene, was used as a base catalyst.
Type of Medium:
Online Resource
ISSN:
1615-4150
,
1615-4169
DOI:
10.1002/adsc.v347:11/13
DOI:
10.1002/adsc.200505161
Language:
English
Publisher:
Wiley
Publication Date:
2005
detail.hit.zdb_id:
2041384-1
detail.hit.zdb_id:
2033084-4
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