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Volumn 38, Issue 3, 1999, Pages 392-395

Enantioselective inclusion complexation of N-nitrosopiperidines by steroidal bile acids

Author keywords

Chirality; Circular dichroism; Inclusion compounds; Solid state structures

Indexed keywords

1 NITROSOPIPERIDINE; BILE ACID; CHOLIC ACID; DEOXYCHOLIC ACID; STEROID;

EID: 0033082647     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1521-3773(19990201)38:3<392::AID-ANIE392>3.0.CO;2-H     Document Type: Article
Times cited : (45)

References (29)
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    • note
    • 2 = 0.200, GOF = 1.094 for all 4485 independent reflections).
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    • A mixture of the complex (5 mg) and KBr (300 mg) was ground and formed into a disk with a radius of 10 mm. The disk was rotated around the optical axis, and the CD recordings were made for several positions in order to check the reproducibility of the spectra. For details of the experimental procedure, see also a) R. Kuroda, Y. Saito, Bull. Chem. Soc. Jpn. 1976, 49, 433-436; b) K. Rasmussen, N. Ch. P. Hald, Acta Chem. Scand. Ser. A 1982, 36, 549-544.
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    • A mixture of the complex (5 mg) and KBr (300 mg) was ground and formed into a disk with a radius of 10 mm. The disk was rotated around the optical axis, and the CD recordings were made for several positions in order to check the reproducibility of the spectra. For details of the experimental procedure, see also a) R. Kuroda, Y. Saito, Bull. Chem. Soc. Jpn. 1976, 49, 433-436; b) K. Rasmussen, N. Ch. P. Hald, Acta Chem. Scand. Ser. A 1982, 36, 549-544.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.