Process for preparation of indenol

Organic compounds -- part of the class 532-570 series – Organic compounds – Amino nitrogen containing

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552 1, 549545, C07C21138, C07D30306

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active

057314640

ABSTRACT:
The invention relates to the preparation of (1S,2R)-cis-1-aminoindan-2-ol represented by formula (IX): ##STR1## and intermediates derived therein.

REFERENCES:
Ito, Satoru, et al: "Preparation of Chiral Allylic Alcohols Using Rhizopus nigricans. Use of the Harada-Nakanishi exciton Chirality Method for Varifying Configurational Assignments of Allylic Alcohols". Can J. Chem, vol. 65, 1987, pp. 574-582.
Didier, Eric, et al: "Chemo-Enzymatic Synthesis of 1.2-and 1.3-Amino Alcohols and Their Use in the Enantioselective Reduction of Acetophenone and Anti-Acetophenone Oxime Methyl Ether with Borene", Tetrahedron, vol. 47, No. 27, 1991, pp. 4941-4958.
Takahashi, etal, Chem Pharm Bull, 43(9), 1585-7 (1995-Sep.).

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