Weight | 157.314 g/mol |
---|---|
Formula | C6H11NSSi |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
2-(Trimethylsilyl)thiazole (79265-30-8)
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- Iterative, stereoselective homologation of chiral polyalkoxy aldehydes employing 2-(trimethylsilyl)thiazole as a formyl anion equivalent. The thiazole route to higher carbohydrates (Journal of Organic Chemistry, 1989)
- ChemInform Abstract: Stereochemistry Associated with the Addition of 2-(Trimethylsilyl)thiazole to Differentially Protected -Amino Aldehydes. Applications Toward the Synthesis of Amino Sugars and Sphingosines. (Journal of Organic Chemistry, 1990)
- SYNTHESIS OF TAXOL AND TAXOTERE SIDE CHAINS BY 2-(TRIMETHYLSILYL)THIAZOLE BASED HOMOLOGATION OF L-PHENYLGLYCINE (Synthesis, 1995)
- Chelation- and Non-chelation-Controlled Addition of 2-(Trimethylsilyl)thiazole to .alpha.-Amino Aldehydes: Stereoselective Synthesis of the .beta.-Amino-.alpha.-hydroxy Aldehyde Intermediate for the Preparation of the Human Immunodeficiency Virus Proteinase Inhibitor Ro 31-8959 (Journal of Organic Chemistry, 1995)
- New organometallic reagents: Use of 2-(Trimethylsilyl)thiazole in acyclic stereoselective strategies (Pure and Applied Chemistry, 1990)
- Carbohydrate Homologation by the Use of 2-(Trimethylsilyl)thiazole. Preparative Scale Synthesis of Rare Sugars: l-Gulose, l-Idose, and the Disaccharide Subunit of Bleomycin A2 (Journal of Organic Chemistry, 1997)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC[Si](C)(C)C1=NC=CS1
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InChIKeyVJCHUDDPWPQOLH-UHFFFAOYSA-N
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