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Volumn 96, Issue 2, 2013, Pages 289-295

The first stereoselective total synthesis of naturally occurring, bioactive (3R,5R)-1-(4-hydroxyphenyl)-7-phenylheptane-3,5-diol and the synthesis of its enantiomer

(4) Reddy, Parigi Raghavendar a Sudhakar, Chithaluri a Kumar, Jayprakash Narayan a Das, Biswanath a

a INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY (India)

Author keywords

Alpinia officinarum; Heptane 3,5 diol, (3R,5R) 1 (4 hydroxyphenyl) 7 phenyl ; Sharpless epoxidation; Stereoselective synthesis

Indexed keywords

4-HYDROXYBENZALDEHYDE; ALPINIA OFFICINARUM; ASYMMETRIC EPOXIDATION; HEPTANE-3,5-DIOL, (3R,5R)-1-(4-HYDROXYPHENYL)-7-PHENYL; KINETIC RESOLUTION; NATURALLY OCCURRING; SHARPLESS EPOXIDATION; STEREO-SELECTIVE; STEREOSELECTIVE SYNTHESIS; TOTAL SYNTHESIS;

CHIRALITY; ENANTIOMERS; STEREOCHEMISTRY;

STEREOSELECTIVITY;

1 (4 HYDROXYPHENYL) 7 PHENYLHEPTANE 3,5 DIOL; 4 HYDROXYBENZALDEHYDE; ANTIEMETIC AGENT; HEPTANE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; DRUG STRUCTURE; DRUG SYNTHESIS; ENANTIOMER; EPOXIDATION; PRIORITY JOURNAL; STEREOCHEMISTRY;

EID: 84874077010 PISSN: 0018019X EISSN: 15222675 Source Type: Journal
DOI: 10.1002/hlca.201200165 Document Type: Article

Times cited : (17)

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