An efficient synthesis of chiral nonracemic diamines: Application in asymmetric synthesis

Tetrahedron Letters

Volumn 39, Issue 1-2, 1998, Pages 167-170

  Saravanan, Parthasarathy ^a   Singh, Vinod K ^a  

^a INDIAN INSTITUTE OF TECHNOLOGY KANPUR   (India)

Author keywords

[No Author keywords available]

Indexed keywords

CARBOVIR; MANDELIC ACID;

ARTICLE; BIOSYNTHESIS; CHEMICAL STRUCTURE; CHIRALITY; REACTION ANALYSIS;

EID: 0031962847     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(97)10578-0     Document Type: Article

References (24)

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11. The β-amino alcohol of this type is very important in asymmetric synthesis. For references, see: (a). Simons, K.E.; Wang, G.; Heinz, T.; Giger, T.; Mallat, T.; Pfaltz, A.; Baiker, A. Tetrahedron: Asymmetry 1995, 6, 505.
12. (b). Wang, G.; Heinz, T.; Pfaltz, A.; Minder, B.; Mallat, T.; Baiker, A. Chem. Commun. 1994, 2047.
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15. Addition of water (10-20 equivalent) was essential in case of other amines as well.
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18. (a). For other asymmetric synthesis of Utenone A, see: Miyaoka, H.; Watanuki, T.; Saka, Y.; Yamada, Y. Tetrahedron 1995, 51, 8749.
19. (c). For racemic synthesis, see Takeda, K.; Nakayama, I.; Yoshii, E. Synlett 1994, 178.
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24. All the new compounds were fully characterized by spectroscopic and analytic methods.