[1]
Luesch H, Yoshida W Y, Moore R E et al. Total Structure Determination of Apratoxin A, a Potent Novel Cytotoxin from the Marine Cyanobacterium Lyngbya majuscula [ J ]. J. Am. Chem. Soc., 2001, 123, 5418-5423.
DOI: 10.1021/ja010453j
Google Scholar
[2]
Mazur R H, James P A, Tyner D A et al. Bradykinin analogues containing N alpha-methyl amino acids [ J ]. J. Med. Chem., 1980, 23, 758-763.
DOI: 10.1021/jm00181a012
Google Scholar
[3]
Ali F E, Bennett D B, Calvo R R et al. Conformationally constrained peptides and semipeptides derived from RGD as potent inhibitors of the platelet fibrinogen receptor and platelet aggregation [ J ]. J. Med. Chem., 1994, 37, 769-780.
DOI: 10.1021/jm00032a009
Google Scholar
[4]
Vedejs E, Lin S, Klapars A et al. Heteroarene-2-sulfonyl Chlorides (BtsCl; ThsCl): Reagents for Nitrogen Protection and >99% Racemization-Free Phenylglycine Activation with SOCl2 [ J ]. J. Am. Chem. Soc., 1996, 118, 9796-9797.
DOI: 10.1021/ja961485n
Google Scholar
[5]
Fukuyama T, Jow C K, Cheung M. 2- and 4-Nitrobenzenesulfonamides: Exceptionally Versatile Means for Preparation of Secondary Amines and Protection of Amines [ J ]. Tetrahedron Lett., 1995, 36, 6373-6374.
DOI: 10.1016/0040-4039(95)01316-a
Google Scholar